Dear Janice,

I just watched your segment this morning on Fox & Friends about your struggle with Multiple Sclerosis. Your story was very moving for me and deeply touched my heart.

My mother lost her battle with this disease just three days after Thanksgiving in 1996. She was diagnosed in 1978.

Medicine has come a long way since 1978 and I am so thankful that you were correctly diagnosed and early enough in the disease’s onset that your doctors have found an effective therapy to treat you. Such was not the case with my mother.

I have always thought you were a lovely individual with a truly delightful personality. Seeing your courageous story this morning made we wish my mother were still alive to see how well you are coping. My mother was a very brave woman throughout her life and she certainly was her very bravest when she learned she had MS.

I will keep you in my heart always with prayers and best wishes. You closed the segment with the words, “I’ll keep dancing until I can’t dance anymore.” My mother did the same thing and when she couldn’t dance anymore her heart took over the dance. She always had a smile for me and endless love.

I tell everyone, “I have diabetes, diabetes doesn’t have me.” Don’t let MS “have you.” God bless you, Janice. May God bless your lovely family as well. Take care.

Best personal regards,

Carol Hall
A friend of Fox & Friends

Janice, I wrote a thread for you at my blog.

Janice,

I admire you for having the courage to share this very personal issue with us. More than ever, I consider you a Goddess. A silly crush has evolved into awe. You are truly a role model.

Luis

Prayers and warm thoughts.

Don’t ever let fear be the deciding factor in anything you do…

Dawn

Dear Janice,

I DVR Fox and Friends Weekend so I don’t miss a minute of it when I wake up. I just watched your segment a few minutes ago. My son is 5 1/2 years old and he has Myotonic Muscular Dystrophy. Anyway, listening to you speak about living a normal life gives me hope for my son. I worry every day about what will happen to him and how he will manage when he gets older. He was diagnosed at 21 months so like you said aboout your diagnosis, we know early on what is wrong with him so we can make sure he gets all the necessary therapies he needs along with the proper medical treatment. People also often mistake his MD for MS. Living a somewhat normal life is all I wish for my son and listening to others like you talk about your life and your accomplishments make me feel like it is possible. Thank you for sharing your story.

Krissy
Loyal Fox and Friends Listener

Janice, you’re awesome. We love you.

Dearest Janice,
Thank you for sharing this with us. I love watching you and enjoy your candid nature on the show. It’s real people like you that make the world go ’round! I have never met you, but I’m willing to bet that you are one of those people that lights up the room when you enter. There’s nothing like a warm, lovely weather girl on a cold New England day.
Hugs,
Steve

Janice,

I was diagnosed with MS in 1992. As with others, you can relate to symptoms from years earlier, but for one reason or another, didn’t pursue it or was misdiagnosed. In the mid 90’s I was feeling a little depressed. I was raising two teen boys (wife passed away years earlier) and traveling around the country at a moments notice and incurring the wrath of self injections of the disease modifying drugs. A “co-worker” I did not know came to visit me and informed me that he also had MS. After telling each other many MS related anecdotes he said to me before he left, “there is really no sense in having this crap if you can’t laugh about it.” I have been laughing ever since and doing great. Also, I believe stress plays an important facctor. I was seeing the neurologist every 3 or 6 months. My last visit I was told “see you in a year.” Retirement a year ago has done wonders. No stress. After 34 years with the FBI I can do alot more laughing. God bless and keep laughing.

Chris

Krissy…

Warm and peaceful thoughts and prayers to your son and the rest of your family…I know your love and support for him will help him deal with whatever challenges he may face in his life….

Warmly
Dawn

Janice,

My thoughts and prayers are with you. I know that you
will laugh and dance your way through this disease.
You are a blessing to all and I love the way
you tell it like it is.

All the best.
Cindy

Janice,

I thought I did DVR Fox and Friends this morning …but the show I recorded started at 8AM and I missed your appearance
(hope to catch it later).

So I read the blog and just found out about your courageous fight against Multiple Sclerosis.
Of course, I didn’t expect it and don’t know much about the disease but in a way, given the fact you are one of the most incredibly positive and genuine personality on TV, I’m sure it is somehow a blessing for all the persons who have MS to have you to speak on their behalf now to all the rest of us and to inform us better.

And I’m actually going to read now the links you posted in your message.

Love you Janice,
you’re so meaningful…
you’re the best!

Guillaume

Janice,

My thoughts are with you and your family. I too have MS I was diaognosed when I was 24, six months after the birth of my first/only son. I’m now 26 and living life one day at a time. My son has been the best cure for me. My husband and Mom bought me my dream farm a year ago. I now live on four acres and have my horses and other animals to keep me very busy. My son and I spend every day enjoying what life has given us. My horses seem to be one of the best therapies for me right now. There calmness and never ending love just lets my body feel free. I don’t feel so alone anymore when I here that there are stories silmilar to mine. Take care and thanks for your strength.

Warmest thoughts,
Erin

Janice,

It takes a truly special person to be able to share something like this with everyone, even folks that you don’t personally know. I always knew that you were a sweet and special woman, and this just further proves that point. You will most certainly be in my thoughts and prayers, and I have no doubt that I speak for everyone when I say I love you. There’s no question in my mind that you will make it through this.

Justin

Janice,

Thanks for sharing a very personal and difficult challenge in your life. I, too, have MS; I was diagnosed in 1989 at the age of 24. I have found that talking to others about MS not only educates them but I draw strength from their responses, as well.

Laughter is a big part of dealing with the good times and the bad news, so never lose your sense of humor

I wish you an abundance of happiness and strength as you face this challenge. Be open and flexible, and always listen to what your body is telling you; you may not like what it says, but it will make your life a little easier if you do.

You are in my prayers,
Kelly

Hey, Janice:

I saw your segment this morning. First, you will always be known as a lady and as the Weather Machine, and NOT AS “that lady with MS.” So, don’t worry about that.

It is always brave to admit to having illnesses, especially when you broadcast it. All I can say is, yes, indeed, you can strive and survive with MS as you put it.

I think that illnesses (in general) are like fear, it is something that you have to put in its proper perspective and the results can (hopefully) do wonders for you.

That’s it. There is nothing more I can say about this, especially since everyone else here says it much better than I can.

Janice-you RAVISHING, RED HOT BABE!

Sal

BTW-I am flattered that you missed my presence here. I did not have a chance to visit the site because I have been taking care of my own issues. No, no improvement on the love life here (you asked me once about it)…being a Fox news watcher is like being a nice guy…we sleep alone. NYC is a very difficult town when it comes to dating.

In any event, the name of the game is for you to continue doing what you do, Janice and for us to constantly watch your broadcasts since we do love you.

Janice, I am saddened to hear that you have been diagnosed with MS, the same disease that Teri Garr and Alan Osmond were diagnosed with. As a fan of yours (and from the Christmas Day 2005 dancing episode to the day you announced your engagement to your husband-to-be Sean [I really loved the Christmas 2006 episode where you modeled the rings], my major crush-now I see why Sean married you), I know that you are very brave and can fight this, and you have the support of your husband Sean (who helped with the NYFD in America’s most tragic time) and us. We love you Janice Dean. Get Well Soon!

Dear Janice; Inasmuch as 3/10-3/17 is MS Awareness Week it seems fitting to add some comments to your blog site. Your attitude re. MS puts you in the drivers seat from the get go. As you evaluate your ongoing response to the vagaries of the disease and the medications you may be recieving be aware that your options now include a truly disease-modifying biological which markedly diminishes the number of relapses and improves quality of life. The choice of treatment options,of course, is a totally individual matter. The most significant factor to stress is that the days of despair re. therapy for this disease are over, and I feel certain that you can find the best treatment regimen available so that all of us can continue to enjoy you at your very optomistic best. All the best—Rey

Janice..

I got up early to watch you this morning..and was broken hearted with your news.. I could see and feel your deep emotions..along with that super inner strength that I know you have. I know I may appear to be a nut-case with my silly southern words sometimes…but I care deeply about people and their pain.. I am glad you shared this…and if anybody can make something good from it, you can..I really admire you Janice,you are beautiful on the inside and out…the world is a better place, because you are in it…and I am proud to be your blog friend…

Love,Deb

Hi Janice,

I was born in Watertown NY and my cousin Marcia Fields now resides in Dexter turned me on to the Newsjunky. I read your blog off the NewsJunky and want you to know I too have MS. I now reside in Henrietta, NY. For years my disease was never diagnosed my earliest symptoms of this disease started when I was about 12 or 13 years old, I would lay in bed flat on my back and my arms and legs would be numb like they had fallen asleep, I was told by doctors that “it was growing pains” or “well your a women”. When I turned 40 years old I had a problem with vertical double vision and went to an eye doctor who told me “Well you need bifocals”. The following year in 2000 I suffered sever double vision horizontally and went back to the same eye doctor who leaped out of his chair, and the very next day I was back to see the neuro-opthamologist in this office who leaped out of his chair and the next day I went for an MRI some people in the office waiting had an appointment one or two months prior, so I knew something was strange. Needless to say I was diagnosed with a severe form of this disease. I work with the most wonderful Neurologist in Rochester Dr. David N. Smith. One thing Janice is never let this disease stop you or anyone with it. Keep the faith. Years ago there were not many drugs if any drugs to treat this disease, but now there are so many. I was on most of the ABC drugs and IV steroids to no avail, but now I go once a month for IV treatment of Tysabri and I have not had what I call an attack for one year, which is a miracle for me, each attack I had caused me perment damage. My right arm feels like a tree limb, but it did feel like a concrete block wall, so I will take the tree limb my vision, bladder, bowels, balance and the ability to walk for very short periods with Canadian crutches. Thanks to my friends were I worked for 24 years when I did not qualify for a scooter through my HMO the people at work took up a private collection amongst themselves and raised $2000.00 to purchase a brand new scooter for me.

My message is hang in there and keep passing that message on, each person seems to have MS in different degrees of MS and some people may never experience what I have and I know I don’t have MS as bad off as others do. Keep praying for better drugs, which are in phase one and two and three drug trials all the time. Develop a great relationship don’t be afraid to ask questions of your doctors talk to them and get their opinions or feelings on what you are saying. WHAT’S MOST IMPORTANT! LAUGH IT’S THE BEST MEDICINE.

Jefferson County has a chapter of the MS society and I am sure they would love any assistance in meetings of the local chapter and the MS walk held in April or May.

Take care Janice keep the faith

Trudy Taylor
Henrietta NY

Janice,
I had missed your segment this morning, but did DVR F&F. I have just now watched your segment and am deeply moved by your story and your courage. You are now permanently added to my daily prayer list of those I love and want to lift up for God’s mercy, strength, comfort, healing, or whatever it may be that you need on a particular day.

Please know that your many fans love you so dearly and hope to continue watching you dance for years to come.

My very best thoughts and prayers are with you today.

Gwen Walton
Collinsville, MS

Janice,

Like the many others who posted before me, I was so touched to see you share your very personal story this morning. I am sure it must have been very difficult for you, but what a blessing your story has been to so many.

Thank you for letting us in, in a very personal way. Thank you for sharing your struggle and putting yourself out there, with no pretenses.

Jenn
Apex, NC

Janice,

The definition of courage is to be scared out of your mind and do something anyway. Revealing that you have a serious illness like MS, whether you did it here on the blog or on the air, shows that you have courage. You rock, lady!

Scarlet Termite

Janice,
You will always be known as The Weather Machine. It is good to have the support from your coworkers and fans and especially Neil, who has lived with the disease for years. Stay strong and don’t lose your sense of humor.

Tim

Janice,
You’re truly a ‘calm’, on many a days when there are ’storms’.

I was dx’ed in 03′. I’ve had 19 infusions, with my choice of a DMD.(Disease Modifying Drug) Like you, no one would ever know I have MS. I’m still dx’ed mild, after 5 years and I’m 54 yrs old. Laughter is truly one of the best medicines, along with a-lot of love and support from close friends and family. I also add huge doses of:
Diet, excercise, supplements, and prayer. This is good a good regiment, even if you’re ‘normal’!

Loved the day you became engaged, the wedding photos and just your ‘true’ daily appearance, on FOX.

Wishing you and yours, well!
Beth

Hi Janice,

I admire you for posting this information about yourself.
You are a strong girl and no doubt you will fight this disease and you will gain victory.

There are many treatments that you should be worry…..If it is not too personal, would you mind share what treatment are you taking at this time?

We all love you and hope to see you strong on your feet as usual.

PJ

Janice – You are a great inspiration to members of the Fox audience. You have so many people pulling for you! It’s been a delight watching you lighten things up over the years. I know we’ll be watching you for many, many years to come. Our thoughts and prayers are with you. It’s just a matter of time before the breakthrough that will lead to resolving MS once and for all! Much love….

Kevin

Janice

Thanks for sharing. I too have MS, I was diagnoses 3 yrs ago, as a single parent I worried what would happen. I felt alone, wanting to know why me, what had I done to deserve this. A friend of mine introduced me to someone who also had MS and after long discussions and support. I started living again. I take one day at a time, I have destress my life as much as I could, which is difficult to do and doing things that I’ve always wanted to do.

warmest thought

Janice, I’ll keep this brief. Thank you for being honest. You are an inspiration to many. We love you and are praying for you!

I’m on dialysis after losing my kidneys to another autoimmune disease, Wegener’s granulomatosis. The disease is different, but we have some circumstances in common.

You have a huge asset working for you. You are a naturally joyful person. That positive attitude will serve you well.

Maybe you should put together an album of Janice Dean’s favorite dance tunes to benefit the MS Society! Throw in a DVD of your best moves, and you’d have a big seller on your hands!

I don’t think I’ve ever seen this many comments on your blog before. I was at church this morning so missed the segment! Is it online anywhere? Would love to see it!
I know this had to be a very scary decision for you to make. I hope that you’ll only receive positive and supportive responses, but you never know with people. I have a dear friend who has MS. She’s such an amazing person and always seems to push forward no matter what. MS seems to be one of those conditions that people know so little about. It could be because it effects each person so differently. There isn’t a list of stages that everyone goes through. What you’re doing by coming out and letting everyone know that you’re going through this, it will help people to understand what it is better and that life does go on and you can face each day as it comes.
Know that you’re in my thoughts and prayers so much. And I REALLY want to see the segment so please tell me it’s online somewhere!!!!!!!

Dear Janice,(Weather Machine,Dancing Girl)
You are so courageous and brave to share with us about your MS;I love watching you on
Fox and reading your blog and the cartoons;you are a blessing to manyof us with your cheerful attitude;praying for you.
Betty

(Lynn…Not sure if Janice is going to post the segment on the blog…I know you can see it here…)

(Hope you dont mind my posting a link to the segment Janice…Feel free to remove if you would rather not ….Which ever makes you feel comfortable)

http://homepage.mac.com/mkoldys/blog/qtb226768915.html

Awww, Janice, bless you and Neil Cavuto! I love you both!

Dear Janice,
Thank you so much for allowing the rest of us in on what is an extremely personal issue. I have had MS for over 20 years and although I am extraordinarily lucky in that I am still so well, it does sometimes scare me. Why does it make me feel better to have someone share his or her story? I am not sure – but thank you! Thanks also to Neil Cavuto for sharing his story with us as well. I wish you and Neil the very best.
Sincerely,
Dianne Wells

Janice,

I am surprised the story wasn’t about this treatment for MS as CBS just did this story in Florida and all of us taking this drug for MS, Parkinson’s and myself for cancer know it is ability to halt disease.

http://www.youtube.com/results?search_query=Low+dose+naltrexone&search_type=

Those taking Low dose Naltrexone for MS can’t say enough about it:
http://www.lowdosenaltrexone.org/

Instead of giving into the disease and doing a program about “awareness” , we recommend you do your research and look into helping all those people who would benefit.

I know it has kept me alive with terminal cancer.

Dee
http://www.ldn4cancer.com

Hi…a Gretawire poster shared your information over there and just wanted to stop by and wish you the best. I have a friend who has had the disease for some 15 years now–she is in her early 50’s and she is doing great! Your attitude is everything and looks like you have chosen some fabulous people for support in Richard and Neil. Truly wish you the best of health and thank you for the good work you do on Fox. And I salute you for coming out, so-to-speak, re having the disease as I am certain you are helping more people than you will ever know…

Janice, you are in my prayers. One day they will find cures for all these diseases. Hope it’s soon.
Neil is a great person, too. Wish you both the very best. I think God picks the cream of the crop to bring things into the open. You, girl, are the cream of the crop!

Janice: You have surrounded yourself with some mighty fine people (Richard and Neil) as mentors! I have a friend who has had MS for 15+ years and she is doing just fine! Thank you for “coming out” as I am sure you are helping more people than you’ll ever know. The importance of a positive attitude can never be denied. God Bless and take care.

Hello,

I admire your strength and your courage to speak about your battles with MS. I was diagnosed September 2004. After struggling through some really depressing times I finally stopped feeling sorry for myself and used the experience as a positive one also. I went back to school and will have an MBA this September. Woo Hoo

I admire your courage to speak out because I still am not comfortable letting people know about this illness. In fact, I know I have hurt some close friends and relatives because they want to show how much they care about me by getting everyone they know involved with the MS walks and I get very irritated with them for putting the spotlight on me. It’s getting better little by little but still very unsettling.

MSWatch used to have chat rooms for people with MS and their caregivers to talk about things. In the newly diagnosed chat room there was a lady named Cindy A.K.A. “HostMom”. This woman helped me and I believe several other individuals through very difficult times. I attribute some of my recent successes to her because she was always so strong, nuturing, and kept me focused on my goals. SHe also has MS.
Unfortunately, MSWatch does not provide this service anymore. I wish there was another site that would offer these chats because it provides some comfort to MS patients when they do not want to unload on their caregivers, friends, and family.

Stay strong
Warmest Regards,
Dani

Hey Janice,

I was just telling my husband 2 days ago that your face is one of my favorite faces on t.v. You are so open-faced. Now, I know you are an open-soul. How brave of you to announce your personal struggles in such a public way. My prayers are with you. Bless your sweet soul, Donna

Dear Janice-

I am a big fan of Fox and also a big fan of yours.

I always thought of you as a very pretty woman, but I know now that you are beautiful inside.

Thanks for sharing your personal story and I will include you in my prayers.

Warmest Regards,

Angelo

Hi Janice

As other’s, I have seen, an enjoyed your weather segiment, you are a brave person, an I’m sure

your husband is very proud of you.

There are many people who can relate too your problem, an doing so creates a real support team.

Just reading through the comments makes one tear-up and realizing how MS effect so many people.

God Bless both you and Neil.

Charlie

Hey Janice, was soo shocked to hear of your illness. I am soo very sorry to hear this but seeing the kind of girl you are, you are sure to get better ! I just want you to know that I will keep you in my thoughts & prayers ! Just keep being the lively,bubbly great person that we all have come to admire & love !!
Hugs & loads of prayers,
Lurlene in La.

Janice…

You obviously have considered today’s announcement for a long time and I applaud you for determining that publicly acknowledging your disease may benefit others. May the attention you draw have a great impact on continued research and, to that end, a positive effect on you.

God bless,

Terry in Indiana

Janice,

A good attitude and a sense of humor are a must when dealing with chronic illnesses. I have long looked to others for encouragement when dealing with my own MS, and I am glad to hear you are doing the same thing.

I believe each of us has our own cross to bear. Ours is a disease which may make our lives more difficult at times, but it can only beat us if we allow it to. My way of fighting is much like yours; I inject myself every day, take the good days with gratitude and the bad days with a sense of humor, and keep on going. There are no other choices.

Good luck to you. I am glad you have joined the ranks of celebrities who are speaking out. You really do inspire the rest of us.

Joanne

Wishing you well, literally…Stay strong

Janice,here’s wishing you well you are a brave person I am sure your husband and family
are proud of you,as you are a sweet and caring person,you are in my prayers and on my
church’s prayer list,also Neil–I wish you both the very best,love and ((HUGS)) Joyce…..

I can save your life, period. You DO NOT HAVE MS. If you want to live a normal life you would contact me. I have spoken to Mr. Bird a long time ago. I have been Nation wide with my Knowledge. Contact me.

Janice

Thanks for your honesty and courage. You are an inspiration. Love seeing you on FOX and will keep you in my thoughts and prayers.

Barbara

Janice,

Why do bad things happen to good people? Be strong and stay positive.

Janice, I am so proud of you, keep dancing and making snow angles~

I was diagnosed August 1981 with MS effecting my eyes and my right leg with numbness that I still have but my eyes are fine~

Your attitude will keep you going, don’t ever give up on anything, I haven’t~

God Bless you and Neal~
Mary in Arkansas

I have a couple of good friends with MS. One of them, I work with every day. For 13 years, I have ridden in the MS-150 Bike Tour…a 150 mile bicycle ride to benefit the National MS Society. This year will be number 14. There’s a place on the number I pin to my jersey where I can write in the names of people I want to say I’m riding for. This year, in addition to my two friends, I’m going to write in your name.

God Bless.

Janice,
My sweet husband just saw Lori Dhue mention that you had MS. I don’t know how we missed your segment this morning,but he came and asked me if I had heard that you had MS. I kept asking him if he was sure he heard her correctly. (I, too, share this uninvited guest. I was diagnosed in 1997 after just waking up completely blind one morning.) The very next thing he said was at least she is willing and able to put a beautiful face and a voice behind this disease. And we thank you for that. We just had our very first grandchild and life just couldn’t be any more fun! She is the absolute joy and love of our lives. I think part of the fight is being around positive people, and you are one of the most uplifting women-with the best attitude I have ever seen. That will help you with those days you have to fight a little harder. Again, we thank you for sharing what I know personally is rather difficult to do. We might have MS, but we just can’t let MS have us! We will keep you and your husband in our thoughts and prayers. Bonnie & Donald

Thank you for sharing the other side of your life with us. I’m sure countless people will benefit from your willingness to share your personal story.

Thanks for the links you included.

Recommend you obtain a detailed mineral analysis of your own hair to provide additional clues for your condition. MS can be worsened by chronic low levels of toxic metals (especially mercury)stored in the body that normally are not discovered in routine blood or urine tests. The hair analysis will reveal if you have a toxic metal problem. If so; you possibly may need chelation IVs and replacement of all dental amalgams, and nicklel bridges from your teeth. I will provide you some good web links to read if you desire.

dear janice, i did not know you had your own blog until today and i will visit often. just wanted to let you know that you will be in my prayers as you deal with the ms. i have a couple of friends that are in the same game with you and have been for several years and they are doing very well. keep your faith and know that we love you and were here with you.

janice you are in my prayers and my thoughts. your an awesome lady and i love seeing you on fox. i have a couple of friends that have ms too and they are doing very well one who lives in nc has had it for years and continues to do well. ill check in from time to time just know that we love you and have your back

Janice,

Thanks for sharing your life with us. It may seem silly but through these words we type each day we all have become a type of family. I am sure others feel this way but I feel as if I ‘know’ you and you in a way ‘know’ me.

Now with me I do not have MS I have contracted inactive tuberculosis. Apparently I got it while in Iraq last year. Inactive is different from active. Active is what Doc Holiday had in Tombstone. Inactive lies dormant in your cells and usually never causes any problems, but as I get older and my immune system starts to weaken then signs of TB could become evident. Right now I am on a 9month 2 pills a day regiment to help fight off most of the TB. Now I am not comparing MS to TB. I am just comparing how we feel when that type of news is given to us. We feel alone. But as you found out sharing with others builds your strength.

Just remember Janice you have tons of people all over the country thinking about you.

Take care,

David

I wish you the best, and hope you stay strong and maintain that great sense of humor you have.

My best to Neil Cavuto, also.

Hi, Janice…I’m a long-time fan of Janice Dean the Weather Machine, and just learned of your MS diagnosis. Bless your heart, I don’t want you sick with ANYTHING, but I know your inner spirit and soul will enable you to forge ahead and live a full and happy life. You surely must feel all the love and support that comes through from your viewing audience, and these e-mails are just the ‘tip of the iceberg’ of support that is yours!

God bless you for your courage, stamina, and the most amazing gift of humor on the planet! You are a joy to watch – who else can tell us it is 20 below and makes us feel like we’re gonna be alright anyway, because her smile is as warm as a summer day? Nobody but Janice Dean the Weather Machine, and she is loved and prayed for 24/7.

A big hug to you and God bless,
Bobbie

Janice,
You are one of the few…the endearing, open, fun, delightful people in the media. You warm my heart, regardless of the temperature outside. To whom much is given, much is required. You are handling your public life and as much of your private life as you choose to share with dignity, honor, and grace. You are an inspiration to me.
Blessings,
Lynne

Hi Janice,
This is a lot harder than it sounds, but please don’t get discouraged. I remember the first time I heard the MS diagnosis, it felt like getting hit in the chest with a sledgehammer. I was diagnosed with relapsing / remitting MS 21 years ago. I did have some minor flare-ups during the first few years, but then I attended two healing services at church and began taking Betaseron injections. The flare-ups stopped right away, but after 8 years I had some liver problems caused by the Betaseron and they switched me to Copaxon. I’ve been on it ever since and the MS has been totally quiet for over 15 years now. I do have some residual numbness, but no visible signs of the disease and lead a normal active life. Once you get past the panic attacks caused by the fear of what lies ahead, it’s just an annoying handicap.
I will add you to my prayer list,
Regards,
Jim
Kodak, TN

You are a smart, funny and brilliant woman.

I can now add “brave” to that list of modifiers.

God bless you, Janice.

Janice,

Man oh man take a break from this and find out about the MS. All I can tell you Man to Woman is keep your chin up dont let the disease run your life. I personally dont know anyone with MS but my Uncle has a friend whos wife has this disease and she has had it for quite a long time and from what I hear about her from my Uncle and Aunt is she is probably the strongest friend they have. I always have my family and friends in my prayers and you may bet you just earned a spot there. Letting the public know takes a lot of guts. And I wish nothing but the best for you and your husband

Janice,
I found it heart warming that you shared this with others..even if we do not have the same illness
it helped me.After being a sober Alcoholic for 28 years i found myself in a severe depression.After seeing Doctors for a few years now i finally have hope.Hope is great after feeling so hopeless for years.
My prayers are with you and your wonderful new husband,Janice so many men would have run.God bless him for staying with you,i love you and think you are so funny and laughter really is the best medicine!!!!!!Keep smiling and being our weather machine.I laughed so when Sheppard started calling you that…………Blessed in Austin

Janice,

I don’t watch Fox, except for Greta, but I just heard about your diagnosis. I wish you well.

I enjoyed you so much when you were on Imus in the Morning, but I can see where those guys can be a bit much.

Stay strong.

Janice,

I don’t watch Fox, so I didn’t see you this morning. I loved you when you were on Imus in the Morning.

I wish you all the best. Hang in there.

Janice,
It is said that they do not know what causes this autoimmune disease (MS), but some say it might have something to do with “leaky gut syndrome”. Don’t know if you have any problems with food allergies or foods that bother you, but you might consider getting yourself tested for “gluten intolerance” and/or “Celiac disease”. “Leaky gut” is just what it says. Because of “food intolerances” it causes the gut to “leak” things into the system that would not normally be allowed through.
You might consider doing some research on this and asking your Doctor about it.
Celiac disease is also an autoimmune disease and gluten is the food that causes damage to the small intestine, which in turn would cause the “leaky gut syndrome”.
Wishing you the best and God’s mercy as you handle this challenge in your life,

Janice,

I saw a small portion of the news cast of your decision to share your story with the public in an effort to help educate the public about MS.

The reason I am writing is because I believe you can be helped with specific upper cervical chiropractic care.

I am a full time student at Palmer College of Chiropractic, when I graduate I will be a 3rd generation chiropractor and number 12 in the family. After I retired from the USAF, I decided to go back to school to become a Doctor of Chiropractic. I am 55 years old and I tell you this so that you know I’m not a young college student that is just excited about my new career.

I recommend that you seek care under an Atlas Orthogonal Chiropractor. I would also recommend that you go to: http://www.globalao.com and view the website. I would also recommend that you call the office of Dr. Roy and Matt Sweat. Dr. Roy Sweat is the Pioneer and Founder of the Atlas Orthogonal Chiropractic Program, and has been a chiropractor for about 58 years.

As you are a celebrity you could also contact Montel Williams as he too has been diagnosed with MS and has been under the care of an Atlas Orthogonal Chiropractor in NYC.

I do want you to understand that chiropractic and chiropractors do not cure anything, we simply find the nerve interference, correct the cause of the interference and that allows the body to heal and repair the way it is supposed to. Your body knows how to heal just like when you cut yourself. As soon as the cut happen, your body begins to do everything necessary to stop the bleeding and for the clott along with all of the other process that occur, you don’t have to make the decisions it just happens.

If I can be of any other assistance I always welcome the opportunity to help people find solution to health related issues. If you have any questions I would love an opportunity to talk to you on the phone, just reply to me with a less public e-mail address and I will give you my cell phone number.

Sincerely.

Corbin Fox

Janice,

I was diagnosed with ms in 1990.

Was able to competitively team rope till 1998 and worked full-time till 2003.

My ms has progressed, I now have the secondary progressive form of the disease, have had a baclofen pump installed and am in a wheelchair.

I’ve long been a fan, and want you to know your “bubbly” personality and great sense of humor will be your strongest ally as you confront this disease. You have plenty of folks to share with, but I found the alt.support.mult-sclerosis group a great place to share and learn.

I still work with the New Mexico State University rodeo team, raise money for the DuBois Rodeo Scholarship program and maintain a news weblog, The Westerner. I’m confident with the current treatments available and your positive attitude that I will be enjoying your forecasts for years to come.

Sending love, encouragement and understanding from way out west,

Frank

Janice, you rule! Very brave for you to come out with your illness in what can be such a shallow business. Hang in there and know that you are also not alone either. We’re all out here too.
Take care and much peace,
patrick

Janice, I have watching you since your days on “Imus in the morning”. I have always been a huge fan of yours. God bless you. P.S. Keep on dancing.

Dear Janice
I have had MS. for 34 years, and I hope there will be a cure soon.
I have been on Low Dose Naltrexone (LDN) 4.5 mgs and it has helped me. It is not a cure but it can slow down MS. and help with systems of MS.
None the MS. Center will offer you any information on LDN.
LDN is a prescription drug in 50mgs prescription. MS. patients take it in low dose prescriptions.
Please check on LDN.
Bless you,
diane

Janice,

Thank you for going public with your MS. I was diagnosed five years ago at age 46. I can track back to symptoms 3 years earlier. I have found a lot of encouragement from watching well known people who have shown they can keep going and adapt. Neil Cavuto and Terri Garr have been my main inspirations along with Montel, Clay Walker, David Landers (Squiggy), Richard Cohen.

I remain happy and optimistic. I take daily injections and visit the MRI machine about once a year. I have not had a new lesion since I started treatment. My walking is variable and my legs tire easily. It doesn’t bother me to use whatever I need to use to get around when I need it.

I belong to a group on MySpace that has 3200 members with MS. They post what is going on with them. From reading their posts it seems their biggest problem is other people, especially family members, not understanding what MS is. This is understandable because it is hard for the person with MS to fully grasp. We just know that we have to adapt because how we feel and how we move changes hour to hour and minute to minute.

Thanks again and best wishes.

MS is a hard diagnosis, as is all of the auto-immune conditions. One thing I hope you have exausted it the possibility that you have Chronic Lyme Disease. Most doctors in mainstream think Chronic Lyme is a very rare condition… I am convinced it is not.

The CDC website says there were 23,000 new Lyme cases in 2006… and also says that the undiagnosed cases were 10 times that number. That means around 1/4 million Americans had a new Lyme infection in 2006. Undiagosed defaults to 1/4 million UNTREATED! But we are told they do not become “Chonic Lyme”, so why do we treate ANY Lyme cases?

The CDC tallies 40,000 new cases of HIV infections in 2006….or 1/6 the number of Lyme cases. The Lyme Literate Doctors will tell you that Chronic Lyme patients suffer similar to late stage Cancer patients.

MS, ALS, Lupus, Rheumatoid, Sjogren’s, Chronic Fatigue Syndrome, Fibromyalgia, and many other auto-immune disorders share as differential diagnosis’ with Chronic Lyme. Only one Lab is consistantly accurate for testing for a Western Blot for diagnosing Lyme… IgneX in Los Altos, CA. Lab Corp’s CD57 may be more useful for diagnosing a chronically ill Lyme person… and Bartonella, Babesia, and Erlichia are important co-infections you need to have ruled out also.

Research Dr. Martz successes with “ALS” patients.

God Bless

Be SURE you do not have an undiagnosed infection that is not politically correct before resigning youself to the MS

When I was dx with MS, I too was afraid to be labeled as the “person with MS”. I have done that my self when I learned of other peoples illnesses. I now know how unfair it is to limit my thoughts to just their illness and not about who they are. Thank you for coming forward.
linda

Janice,
I hear you girlfriend. I truly understand the why and the need to do this! What does not kill you only makes you stronger is the battle cry for many cancer survivors, and with MS I am sure it is also true. Every day you feel great celebrate it as your last, because this is not a sprint race this is a journey. A journey that takes days, weeks, years to make. And that my friend can get you through the yucky times, the sad times and the great times.

You are being brave by going public, I am grateful that you are. MS can be well managed a lot of the time, there is a friend I know that has it. He still works fulltime and is very independent. His business is booming, he has hired the right kind of people and they serve him well.

Neil has been incredible, I watch him with awe!

Just remember to live your life no matter what the sign on your forehead says. Love your spunk and your candor.

ms
i had a sister that had ms and she lived a good life. go on a glutin free diet and you will be better off. read lots of labels. she had a very bad type where she shook all the time. but it didnt stop her from enjoying life. she had the best sense of humor. she told my mother one time that she and i would open a business. shed be the soda jerk and i would hand them out. there is more known today then when she was found with the desease. god love you and stay bright. sue

Janice,
I am proud your segment on Fox Sunday about multiple sclerosis awareness week, and the fact that you also suffer from M S.

I was finally diagnosed with M S in 2006 after 4 years of tests for this, that and everything else. I have never had anything come easy to me since a genetic heart disease that struck me in 1995. Every doctor that I saw at The Hershey Medical Center in Hershey, Pa were looking at my symptoms from a cardiology standpoint.

Just before Christmas of 2006 a pharmacist saw me for my routine blood test and he insisted I see a stroke neurologist. I met with the man in March, and after a routine neurological exam he was willing to come to the conclusion that I had M S, and since I have a pacemaker I was unable to have an MRI, so I was given a lumbar puncture and his diagnosis was confirmed. After a 5 day I V steroid treatment and then being placed on Rebif, I am able to walk again only with the aid of a cane and an orthopedic brace.

I have what they call secondary progressive M S, in that when I have an attack I am usually stuck with what ever the attack affects. I have a severe Right Dropped foot in which I have to wear a brace in order not to stumble over my foot as I walk. I also have other symptoms such as bladder control, a slow digestive system, numbness sin my feet and hands, but because of the medications I am on I can still function what I consider a normal life.

I was able to continue to work until November of 2007 as a dispatcher for a major refrigerated trucking company, but my wife and I both felt that it was time to call it quits because of all of the stress from the job. It was not the M S that made me retire, but more my heart condition. I guess I am one of the lucky people though, I can get my insurance through my wife’s employment, and God enabled us to sell and buy a smaller home that is more M S friendly meaning there are no steps in it.

I feel honored that I am still able to get around and still do some of the normal thing in life such as drive, go shopping, cook, and yes even clean and do the wash for my wife. From the first day I was diagnosed with M S, I was not going to let M S control me, but I was going to control it.

My whole family supports me every day along with my neurologist and his nursing staff. There has not been one time that when I have had a problem that my doctor has not called me and helped me with any issues that I have had. But more so than the people that I have mentioned above the support group that I attend every month has been a God send to me. It has been through these people have I obtained not only support, but helpful hints and ideas to help better myself live with my M S.

If I have one complaint, it is the people you mentioned in your segment, and the people organizations such as MS lifelines tend to showcase as there ambassadors with M S. Just once would I like to see someone or some organization do a profile on people with secondary or primary progressive M S. To show the struggles these people go through to do ordinary tasks of daily living. My youngest daughter said it best when she once told me that she was thankful not to have to struggle to do ordinary things such as getting in and out of a car like I have to.

I am 56 years old and my doctors have told me that I probably have had M S since I was 40. My three grown children jokingly call me an old goat, but this old goat has always remembered this one saying that was voiced during the confirmation hearing of Supreme Court Justice Clarence Thomas. It was said that he just pulled himself up by the boot straps and kept on going. What wise words to live by when one has M S.

Dave
Lancaster County, Pennsylvania

Janice,
You are ALWAYS a bright light on Fox & Friends. With your weather reports, your dancing and your banter, you bring energy to a DECIDEDLY NON-ENERGETIC time of day. The way you are handling this diagnosis tell me there are fists of steel in your velvet glove personality. God Bless You and Keep You.

Janice, sorry to read that you have MS. But I’m “happy” to read that your MS is treatable. My sister-in-law is not so lucky. Her MS is progressive. She can’t walk anymore. She is in mild heart failure because of the chemo she received as a treatment for MS. I wish you could send her an e-mail of encouragement. If you can see my e-mail address e-mail me and I’ll send you her name and address. I am admirer of Neil Cavuto. And now you’re on my “list.” Take care, Janice.
Best wishes…

Janice,
You are a true treasure. Your smile lights up all that are lucky enough to catch your work on FOX.
Stay tough kid!!

Janice,

There apparently is a strong correlation between drinking diet sodas with Aspertame and MS-like symptoms. If you are a diet soda drinker, you may want to try eliminating them to see if your condition improves.

I have read that “When the temperature of Aspertame exceeds 86 degrees F, the wood alcohol in Aspertame converts to formaldehyde and then to formic acid, which in turn causes metabolic acidosis. Formic acid is the poison found in the sting of fire ants. The methanol toxicity mimics, among other conditions, multiple sclerosis and systemic lupus. Many people were being diagnosed in error. Although multiple sclerosis is not a death sentence, Methanol toxicity is!”

I hope this information proves to be helpful.

You might look into getting a Segway for help in getting about. My Segway has certainly been life-changing. Check out Segs4Vets.com. Many amputees are benefitting greatly.

Janice, we love ya, we will put you on our prayer list…..you are special to all of us out in Fort Riley, Kansas area. Thank you for sharing yourself with us, your viewers, your friends.
Testimonies always help others, yours I am sure will touch many.
Blessings to you and the hubby.
Kathy Felix

I hope you do well. From one who has it, I could give tons of advise, but you’ll receive plenty of that. Main one, stay fit or get in shape while you can! I also hope you don’t face employment problems and lose your job too. Take care.

hi,Janice!
Wow..I am surprised..
Glad to see that you obviously are doing well..
I am glad also to see that you have a place to make people aware..
Although I know that the news anchors,and weather anchors we see on TV daily are ordinary people like me and all.I think it’s so important for those that feel they can use a blog to share feelings like that of personal things like triumphs and things they are going through to remind us that you are not just a face on TV but a person too.

I was diagnosed in 1985. The key is to tell yourslef that you CAN beat this thing. I sometimes am forced to use a cane, but I will continue to fight every minute I live to maintain a similitude of normalcy even though MS will continue to fight back! Never give up. I made a promise when I was diagnosed and this is what I promised myself and my God: “I will greet each day as if it were my very first, and I will live each day as if it is my very last. Be strong.

Janice – It is hard to believe that you have had MS for 2-1/2 years and yet resonated this cheery, up-lifting attitude as the “weather machine”. Somehow I missed the episodes where you announced your engagement and showed your wedding/honeymoon photos. (Boo-hoo)

We use to be Imus fans and witnessed when he hired you. You were this girl from Canada as is my husband. What you do at FOX is so much more appropriate for you than the Imus gig. You
definitely made a good decision when you went to FOX. You and your personality just blossomed. We really enjoy seeing you being your cheerful (sometimes silly) self. We feel like we know you and were saddened to hear that you are faced with this health challenge.

It is obvious that you have reached a place in your life where you are able to give a voice to this
disease and by encouraging others in turn it helps you. What a great girl you are and your family must be very proud of you.

We will continue to wish you well and pray God will always be with you.

Congratulations and best wishes on your marriage!

Carolyn

Janice,

It is great that you decided to come forward. Far too many afflicted with this disease will not or are afraid to. I applaud you for your candor and courage. I also commend Neil Cavuto for his courage. By virtue of your positions awareness can be made at an all new level. I think Bill O’Rielly needs to interview the two of you and raise public awareness.

My name Robert Wolz and I am a retired SFC from the US Army. I served 20 years + as a Chemical, Biological, Radiological, Nuclear Specialist. I had 2 tours Korea, 2 tours Germany, Gulf War, Operation Iraqi Freedom, and various stateside units. I grew up in Louisville, a 1983 graduate from Bishop David High School. I am not currently residing in Congressman Yarmuth’s district, however, the rest of my family does.

I have remitting-relapsing MS. On February 21, 2008, I spoke at a Congressional Briefing Examining MS among Veterans. In an effort to secure $15 million appropriation specifically for MS research in the Congressionally Directed Medical Research Programs (CDMRP) through the Department of Defense. In 2007, the work of a strong coalition paid off when MS was listed as a research area eligible to compete for funding through this program for the first time. This year, we can work to secure a specific appropriation for MS research.

Congressmen Russ Carnahan and Michael Burgess, M.D. released a Dear Colleague letter in the House of Representatives that requests the House Appropriations Subcommittee on Defense to include $15 million dedicated to MS research through the CDMRP.

New evidence shows a potential link between the incidence of multiple sclerosis and combat service. A recent study in the Annals of Neurology identified 5,345 cases of MS among U.S. veterans that were deemed “service-connected

Dr. Mitch Wallin, an Associate Professor of Neurology at Georgetown University School of Medicine and Associate Director of Clinical Care at the Department of Veterans Affairs MS Center of Excellence-East in Baltimore, shared his experience treating members of the U.S. military living the disease and his findings on the increased risk of MS among veterans.
See story at link below.

http://www.courier-journal.com/apps/pbcs.dll/article?AID=/20080222/NEWS0101/802220390

Good luck, I know what you are going through. But having a supportive family really helps.

God Bless,
Bob

Dear Janice

You don’t know who I am but by way of introduction, I used to anchor at CNBC and Bloomberg TV, a little Court TV and CBS. I know a little bit about survivng bright lights and negativity this business and this world can bring.

And as much as I think I have endured, I must say it’s stories like yours last evening that put everything back into perspective.

I honor you for your courage, your grace, your beauty and your steady work on Fox. I now also honor you for doing so in the face of a condition that surely frightened you and may still. I have seen the pictures of your wedding, heard you graciously kid with other folks at Fox and admired your work for many years. Now I am humbled by your path.

People like you do more good for others than you may ever realize. Thank you for sharing and good luck in your continuing inspirational path. You will be in my prayers.

God Bless you and yours always
Bonnie

Dear Janice–I am so sorry to learn of your MS diagnosis. Your charming and delightful demeanor have been a source of inspiration to me since you joined FOX, but even more so now that I know that you’ve been dealing with such a “real life” problem these past 2 1/2 years with such grace and good cheer.

You’ll be in our thoughts and prayers and we’ll toast you every night! Stay the winner we all know you to be!

God Bless You, Janice. I have Chronic Fatigue Syndrome, and was inspired when I read an article about Neal Cavuto – how he finds ways to compensate for his symptoms so he can keep working. I saved that article on my computer and titled it: “When I Think I Can’t”.

When I’m having a bad day with the CFS, I think of Neal and his strong spirit, and that inspires me. Now I will think of you, too. Thanks for having the courage to share!

Love and Best Wishes,
Liesa Healy-Miller
Framingham, MA

Dear Janice,

As a devoted viewer of Fox News, I’ve been constantly amazed at the level of courage and integrity that your organization provides. You join such fine examples as Neil Cavudo, himself suffering with the same illness. Other colleagues of yours, while not enduring significant illnesses, demonstrate the strength of their convictions and devotions in an increasingly sterile and secular world.

I will be watching you and your friends every day. Your positive example, together with those of other luminaries of faith at Fox News, is a constant encouragement to me. May God richly bless you, send you healing, and enfold you in His presence like a warm blanket.

Warmest regards,

Bruce

Dear Janice,

I have had MANY health issues, to the point of walking with a cane in my twenties.
I went from specialist to specialitst. What has helped me the most with a FMS/cronic thyroid
and damaged organs is….. traditional acupunture. It has changed my life. I am on
specific natural supplements for my conditions and recieve treatments that I need.
That is the beauty of acupuncture. It will be what you need. I strongly encourage you to seek
a traditional acupunture dr. You will be amazed.
You will be in my prayers. Take good care.

Sheri

PS havent used the cane in 6 yrs and counting

Janice,
Your a very strong person to come forward. I also have MS and I have refuse to let my life change in any way. The truth is my life has become better. I appreciate things more, my eyes have opened and I am strong!

I admire you and also Niel. I have always looked up to Niel, he has been my inspiration and now you too will also be another pioneer. Keep the faith!

I enjoy FOX News and have and hope to continue to enjoy watching you.

Hi Lady,

You are a very brave lady. I was sadden to hear about your illness, however, it seems you have accepted it and will make the best out of the cards that the Lord has delt you. I will pray for you and wish you the best in the effort to live with the illness. God Bless you and your new husband. By the way, my son is a weather forcaster in the Air Force. You do a good job and so does my son. Best of luck and stay safe.

Sincerely,
Wendell

WOW! I know I admired you for a reason, other than your bright personality and leeting the viewers in on your life. I too have MS and have been very vocal about how the diseace affects me. I have all the hidden symptoms, the one,s that make everyone say, Really, no way, you look so good!” I beleive that God not only graced me with the disease, he also gave me the grace to deal with it. I can tell you that when I was diagnosed 12 years agao (Martin Luther King Day 1996), my children were not quite 3, 5 and 9. So my children have gown up with the disease I tel;l everyone, it is my best friend, because it is alwasy with me and we don’t get along all the time, but it is always with me. My kids and husband can tell when my MS is flaring better than do. They see it in my actions and on my face. My oldest was diagnosed 3 years agao with Spondylitis (arthritis of the spine) also an immune system disease. She says that my MS has helped her to deal with her disease. I beleive the more we all talk about our lives with MS, the better off we will all be – maybe someone we talk to is struggling with the disease, or we inspire a scientist to fight it, or someone to give money to reasearch.

I will end my soapbox now, I just wanted to thank you for speaking out… and welcome to our world!

Regards,

Sara, NC

From http://testimonials.silvermedicine.org/content/ms-cured-argentyn.html

“…August 2002

My MS Update This is the second anniversary of my long, but wonderful journey with colloidal silver (CS). I am a 59-year-old female who had relapsing remitting MS for 31 years. About 1995 it changed to secondary progressive MS. Thus began my long road of decline. Everyday I got worse. When I discovered CS I could barely walk. I was beginning to use a cane. I could not even go up on the curb without aid. My prognosis was grim. I had some knowledge of the great properties of silver, so the idea of CS intrigued me. I researched CS. What did I have to loose?

I began drinking 16 oz per day. In about three weeks I began to notice a difference. You already have a log of my first year’s progress. I seemed to reach a plateau about this time. I did not improve, BUT I never got worse.

I have since had an MRI and it showed that at this time Aug 2001, I no longer had MS. I have had no new lesions for well over a year. What I was working on at the time is to now repair the damage. Since the damage is to the myelin and not the central nervous system, I was quite confident I could improve…”

Thank you for sharing Janice! I was DX two years ago April and it is so inspiring to see others, like me, out there working and trying live their lives of “new normals.” Good luck!

T

I was shocked when I saw the headline on everythingcody.com about you having MS. My mom has had MS since the late 80’s. I was further surprised to read your story and find out that another one of my favorite Fox News people, Niel Cavuto, has MS. You have done well by talking to people that know the struggles of living with MS.

My mom is involved in a western music group (Sons of the Pioneers genre). She too is used to being active, but she has had to learn to budget her energy.

It is amazing how much the weather can affect someone with MS. When Mom is feeling not so great, she always comments that there must be a change coming in the weather. Inevitably, later on that day, a storm will hit, even if brief.

Hang in there and keep on keepin’ on.

Janice–You are always such a delight to watch on Fox–so full of joy and enthusiasm. You’ve been an inspiration to me –even more so now since I learned you’ve been fighting MS for 2 1/2 years.

You’re a winner, Janice, and you will prevail! We’ll keep you in our thoughts and prayers and toast you every night!

You were an inspiration before your disclosure, you are more of an inspiration now, Janice!

We (others with MS) are here for you!

Thanks so much for being vocal and unafraid!!
..MS already has power and control… no need giving it an ounce more!

My husband has MS he was active duty Army since he was 18 and at age 35 had to do a Medical Retirement,and the stress does have a factor in his illness and i believe if you can live stress free it does help with it and also i believe that marijuaina is a good thing and should be legal for ppl with MS and other dieases,so support to leaglize it everyone that reads this blog, but have it controlled of course.

Lisa

janice, I just wanted to let you know I think your great and my husband likes you to cause your so real……….I am being tested now for ms…..but my prayers are with you and your husband and family. I know that this is scarey but with God’s help we’ll all get thru this………….I love watching you on tv and how funny and happy you seem.send me a picture of your wedding. I didn’t get to see it………but I am sure you were a beautiful bride……take care and tell neil cauvuto I admire him also. My prayers will always be with ya. sincerly diane layman/galveston,texas

hi janice- from the first time i saw you on fox, years ago, i liked you and could tell how nice you must be. and i know, know know you will be fine and there is no question about it and i will pray for you too. i think anybody who ever saw you had to say to themself, what a great person she is!

Dear Janice:

It was in the midst of Hurricane Katrina that I realized I was facing storms within and without. I lived in the area that was hit by Hurricanes Katrina and Rita within weeks of each other. I worked for 39 days straight in the aftermath of the storms without. Went to the hospital less than two months after Katrina, had the right breast removed and returned to work four days later. I managed to work (well, at least be there) through 8 chemo treatments. I’ve since moved from Ground Zero and have the energy to enjoy six grandkids. Also I provide part-time child care for an adorable red-headed two year old boy who can throw a football like a professional, has read (or listened to) more books than many high schoolers and is teaching me to see the wonder of the world through the eyes of a child.

You are going to make it!!!!!!

If you ever need anything from me — inspirational advice, a good joke or an e-hug I am just an e-mail away.

Jean
Ponchatoula, LA

janice, you are a winner and you will win!

Janice:

I salute your courage!

I’ve always enjoyed your rapport with Sheppard Smith, but now I can also look up to you as an individual.

God Bless You and keep up your sense of humor.

Regards,
John Markowski

Janice…..

Thank you so very much for sharing your life with all of us. I am a TV Meteorologist and I work in the Denver market and have since 1977. I have been very active with helping to raise money and awareness for Juvenile Diabetes and I feel honored to know that a fellow Meteorologist is just as human as the rest of us.

I have enjoyed your weather reports on Fox and will continue to do so. By the way, congrats on your recent marriage and please tell Megan Kelley, congrats on her recent marriage as well.

God bless you and your family and my thoughts will be with you in your journey with MS. Stay strong and keep a smile always.

Sincerely,

Rob “Sunny” Roseman
KGWN Channel 2 – Denver

i read a good article a couple of years ago of a young girl who walked with leg braces. she got information from someone about horseback riding helping ms patients. she tried it at an equine handicap facility and to her amazement it really helped her, so she bought a horse and threw her braces away. she says that she rides everyday so that she can walk. maybe worth a try if you like horses. God bless you through all your trials alvin

Thank you for doing this giant step! I am a MS self-help group leader and I remember well the feeling to want to talk to someone who has MS, who understands the fear I felt then!

I hope your journey with MS continues to be only a inconvenience but if it develops into more you will face it with courage and come through it a better person.

God Bless
Brenda

Janice( forever the weather machine),

As all the comments I have read indicate, you are LOVED and ADMIRED for your courage and forthcoming attitude towards this problem. I am amazed every day at your positive, bubbly outlook towards life. Your smile is like a beacon of happiness in a sea of depressing news and I look forward to your banter with the hosts, esp. Shepard Smith. We will pray for you and keep your family in our thoughts.

You are in great hands with the fox family and its viewers.

Bless You

Janice…you are the weatherperson I have been in love with for a long time. You,along with the rest of the fox crew come across so human, humble,lively and great. I constantly remark to my wife that all of you look as though you are having so much fun,every day.
I know that with your positive attitude , great fox friends and fans you will push thorough this and all of the attendent factors in the future. I look forward to seeing you and following your career for the rest of my time here.
My best respects to you and all the fox group!
Larry Uloth
Gum Spring, VA

i have always liked you JD, but now i realize just how special a woman you are!! my best to you and your hubby during this difficult situation.i know God has a special place in his heart for someone like you.Janice you truly are a sweet,classy woman.

Hi Janice,

I want to refer you to a charity called Direct MS. Their webstie is: Direct-MS.org

I urge you to read all of the information there as the diet and nutritional recommendations given are proven to be successful for people with MS and Transverse Myelitis (which is what I had). After a year on this regimine, an MRI showed that the leison on my spinal cord was gone. I have read many, many testimonies of people who had severe cases of MS who are living normal, healthy lives since adopting the recommendations listed on this site.

Very sincerely,
L. Hatam

I commend your step and wish you the best in the battle and in the journey. I went a bit differently in my choice way of fighting but whatever the direction I suggest that one look for quality years more than quanity years. Who wants a marker that says “died and fifty buried at eighty”? Who wants to just exist? Blessings. Chaplain Bob

P.S. Just for the record I turn eighty this years and still hike miles and enjoy quality living.

Janice,
I am sorry to hear of your diagnosis. If you have not already done so, consider having your mercury levels measured. A “challenged” urniary test is inexpensive (about $60), covered by most insurances and offers some real insight.

I was also diagnosed with MS, but delved further into the matter and discovered I had mercury poisoning. Once I had all my the dental amalagam fillings (which are 50% mercury and vaporize constantly) replaced, my “MS” disappeared. I have been told by physicians at leading hospitals that MS is one of the leading misdiagnoses of mercury poisoning. Mercury poisoning is not uncommon, and I urge you to share with your readers that it is worth pursuing particularly if they have dental amalgam (silver colored) filliings, get frequent flu shots which contain thimerosal ( a mercury preservative) or eat excessive fish and sushi. The very best to you. Susan

Hi Janice,

You will be fine! I am glad you have friends like Neil Cavuto who know exactly what you’re going through. I too, have MS, diagnosed in 1999 but symptoms since 1995. Life does go on, I inject myself daily too (Copaxone), yeah, it can be annoying but I thank God my MS has remained stable.

You will have good days and bad days just like everyone else. Researchers have come a long ways and hopefully, in our lifetime, they will find a cure.

Stay strong and hopeful!

Raylene Nance

Hi,

Naltrexone is a medication approved in 1984 by the U.S. Food and Drug Administration for treating heroin and opium addiction In very low doses, it is proving to be amazingly effective in treating multiple sclerosis–with minimal side effects and at a price anyone can afford.

For more information about Low Dose Naltrexone in the treatment of MS, visit

http://tinyurl.com/2boot2

With best wishes,

Dudley Delany, R.N., M.A., D.C.

As someone diagnosed with MS this past January, I just want to say thank you.

Hi Janice.
I have followed your illustrious career since you were on Imus in the Morning and
put up with his ‘BS’ while pushing his toothrbush sponsor ‘brush like a dentist!”

I have always admired your spunk and your positive attitude–even on those mornings when the Imus Chauvinists put you through their ‘makeover’ and other miscellaneous
demeaning Animal House rituals!
I love your weather reports now on Fox and I know Shep loves to volley back and forth with you and you always have a wonderful sense of humor and attitude which will certainly carry you through this time and whatever you have to deal with in your future–

You are not only liked out here in TV-Land–I venture to say you are admired and loved by those of us who know your work as you always have a special light around you even when your forecast is for overcast and gloomy weather.
Trite as it sounds, you are in my thoughts and prayers and somehow I trust you WILL
be stronger for what you will go through.
Take care of yourself and keep that fabulous sense of humor–if Imus couldn’t bring you down, a little MS is certainly not going to succeed!
Best to you and yours-
Ann Darling–(Still a crazy masochistic Imus-watcher even on RFD!)

You go, Janice! I’ve always admired you for being so happy and peppy on the air ALL the time! Little did I know you were hiding a big secret. I am cheering loudly for you (and Neil.. and everyone else) to beat this big bad MS disease!!!

God Bless you, and know that faith, family and friends will keep you STRONG!

Janice, your courage is amazing.
Bless you and your family.

I wish you the best in everything. MS is bad, but early dignosis can help you to live a relatively normal life. Best of luck.

Ms Dean,
I’ve had MS since 1980, when I was diagnosed after going blind in my right eye. I’ve had quite a few excerbations during the next 20 years. Almost all of them varied in intensity, duration and location. I’m SS disabled now. However, I can walk without assistance, albeit short distances before resting. I also take injections once a week and have now for over 7 years. MS has required some adjustment in lifestyle, working conditions, and family association, but not necessarily negatively impacted my overall life.
The first blessing from this cloud, for lack of a better term, was that it forced me to re evaluate just exactly what was my most important priorities in life. I knew now that bad things could happen to me. This gave me an advantage over other people, whose priorities were more materialistic and monetary. Those are not real reasons for well rounded and healthy mental stability. The result of this evalution required me to revise my personal convictions as to the important things in life. One of those, was to overcome any disabling effects by experimenting with different hobbies, occupations, and schooling to permit an active, enjoyable, productive and independent life to the best of my disability. This has led me to a varied and most enjoyable overall time for my life.
I live in a remote area of Alaska, population 3. My wife of 36 years and a full time crew member. I live on the coastline of Prince William Sound on my 5 acres of private property surrounded by 20 miles in every direction by property owned by the federal or state government designated by forest or parks. I probably would not have tried to live a Thoreau type lifestyle, had I not been diagnosed with the disease. I’ve lived here full time, summer and winter, for over 2 decades and have never regretted the decision.
I just wanted to give you a little background as I was in a similar employment position, when I was diagnosed. I was the second highest official for the Electrical Workers Union IBEW, which covered the entire State of Alaska. My occupation was a power lineman working high voltage electric lines. Obviously with weakened legs and numbness, I could not continue working this trade. It would be extremely hazardous to myself and crew. I was devastated that I had to quit this work, as I really liked it. So, on to different and better things.
Your decision to discuss your condition is a good sign that you have accepted the potential effects of the disease and are going to deal with them in a positive manner. This is a mental stage that with everyone I’ve talked who has been diagnosed, has finally arrived at. Some sooner, some later. It is after this individual acceptance and positive outlook that living for the now becomes more important than living for tomorrow. You will appreciate the roses a bit more than before, appreciate your fellow man with a bit more compassion, and appreciate your family a bit more than you might have normally. You will also notice a substantially reduction in your stress levels. This reduction is actually beneficial, in that stress has been indicated to initiate MS attacks. The object in the disease’s control is to reduce the length, duration, and quantity of attacks. If stress aggravates attacks, then it must be eliminated or reduced to prevent occurences.
I wish you the best and think you are on the correct pathway to living a nearly normal lifestyle. One in which you may look back upon with surpise.
Sincerely
Greg Williams
Falls Bay, Alaska

Janice

God bless you for your for both your forthrightness, and your bravery. Every day you step in front of that green screen you do the viewers a favor….not just by telling them about the weather, but how to address life when things are not exactly 100 percent peachy-keen.

My cheers, and prayers, are always with you.

Best Regards,
Larry Cosgrove

Hi Janice,
Thank-You for going public with this sometimes very invisible disease. The more people that share their story, help those of us that do sometimes feel alone with this crazy and sometimes annoying disease. Back in 1994 I was diagnosed with MS. Misdiagnosed for a number of years. Looking even farther back onset was in 1987 or earlier. So I’ve had this for over 20 years. The onset days were so frightening! Numbness and tingling that would magically disappear once moving into an airconditioned environment. The extreme fatigue is the most difficult to deal with. Or a leg that just did what it wanted. I have just recently suffered an attack that affected my vision. It is not fully back. I have faith it will. I have also started taking Rebif very recently. We will see how it goes. I hope others feel free to share. Don’t be afraid to say no to people. They will understand.
Love yourself and take time to rest even if it’s for a half an hour. God Bless you.

Thanks again Janice. Take Good care.
Lisa

Just proves that you are as beautiful inside as you are on the outside. God will continue blessing you as you do those things that you are meant to do. We love you!!

Janice:

Being in broadcast, you probably have more friends than you can imagine. I have always enjoyed your presence on Fox News.

You are added to our family’s prayer list.

Reg

thanks.

Janice, bless you for your brave transparency. I pray that you are one of the ones who responds well to medication and that you will remain joyous through this journey.

First, I’m sorry that you were diagnosed with multiple sclerosis. I have a few colourful metaphors that I like to use to describe this disease, but I shall refrain as this is a public forum.

I facilitate a support and swim group for both those diagnosed as well as for their caregivers, and their problems and successes run the full spectrum. I hope your course of this disease stays on the relative easy side, but I can tell you that your approach to it is spot-on perfect and I have no doubt whatsoever that you’ll be fine regardless of how it eventually progresses.

Thanks for sharing this, Janice. You did a good thing.

Janice,

How courageous you are! Your persona on tv has certainly not given me any clue. You appear to me to be vivacious and even a little honery.

We, my wife and I have some insight into your situation. She has since been diagnosed with gastral paresis and has peripheral neurapathy. At first they folk at Mayo thought it might be MS. To date, no reason has been given for the paresis.

I do not intend for this to be about us, my apology. What I want to say is that I as a pastor have watched many of my parishioners struggle with all sorts of disease and brokenness. Over the years it has been fairly consistent that those who do their best to continue to lead “normal” lives are the ones who are most successful. They are also the ones who experience the most joy in the midst of their trial.

I won’t preach at you. But I will pray and I have seen miracles, so I pray you experience your own.

Blessings to you and yours,

Brian

I understand. My wife has some wierd disease that has no name yet gives her symptoms of a variety of neurological diseases. She faces an up hill battle every day, yet she remains up beat (most times) and always my hero. It was hinted that she too may have MS, but that was discounted a couple of years ago. So, we march on. Dealing with life on life’s terms and I guess that’s the way it ’s suppose to be. Some day, she will know what’s wrong.

Janice, I have watched you for a few years on the Fox Network. You have been serious when need be, but also hilarious when the moment was right. Keep the faith and all will be well. Cures are around the corner, just have to get there.

Len

FIRST OF ALL, GOOD LUCK TO YOU AS YOU FIGHT MS. I HAVE SEEN YOU ON FOX MANY TIMES AND ENJOY YOUR WEATHER FORECASTS BECAUSE OF YOUR EASY GOING STYLE. ALTHOUGH YOU TALKED ABOUT HOW DIFFICULT IT WAS TO MAKE THIS ANNOUNCEMENT, I AM SURE THAT YOUR OUTGOING PERSONALITY AND WORK AND FAMILY RELATIONSHIPS MADE IT SOMEWHAT EASIER. I JUST HOPE THAT HOW YOU HANDLED YOUR ILLNESS PROVES A MODEL FOR OTHERS WHO FACE THE SAME CHALLENGE IN THE FUTURE AND ARE NOT SO SELF CONFIDENT OR WHO DON’T HAVE OTHERS THAT THEY CAN TURN TO. I ADMIRE HOW YOU HAVE HANDLED THIS, AND
WISH YOU THE BEST IN THE FUTURE.

Janice,
you really are a beautiful person both
inside and out.
I’d like to recommend a book to you:
“You’ve Already Got It!” by Andrew Wommack

Your friend in Christ,

Nick Schiefen
Houston, Tx

Janice~

Welcome to the club that nobody wants to be a member of. I was diagnosed in 1999 and felt like my world had crashed down on me.

Now, 9 years later, I have donated my body to science in the form of a clinical trial for the new medication on the horizon, Fingolimod (yes, hopefully they’ll come up with something catchier before it hits the market). It’s a once a day oral medication and in earlier trials it had wicked results at keeping the MS attacks at bay. Hopefully you won’t have to be a pin cushion for much longer. I was on Copaxone before so I know the stinging, burning, itching lumps well.

Thanks so much for sharing your story with us all. That took guts. Do remember, tho, that you are a weather lady, someone’s daughter, perhaps a sister, a mother (?), a friend…you are many things. Don’t wear the MS label and forget the other stuff because it’s easy to lose your sense of who you are despite the disease.

I had my EDSS assessment for this clinical trial last week and the doc said I’m doing really great for 9 years out. You can’t even tell by looking at me that anything’s wrong and I walked the whole 500 meter walk unaided. That should be encouraging to you.

Here’s wishing you the best! I’ll be rooting for you from the sidelines.

Jeri

PS, what’s the weather going to be like this weekend for NE Florida? Hey, can’t blame me for asking.

JD, TWM,

GOD BLESS YOU!

I hope He blesses you with additional strength to carry on. I became an adoring fan when you were on Imus. Your laughter makes me laugh. Your incredible smile makes me smile and your rye wit is best of all.

I have one regret. I have not seen JD, The Dancing Machine clip. That is still accessible isn’t it?

I am new to blogging. I got my start with your compadre, Alisyn Camerota’s blog. Anyway, if and when my wife and I can make it to NYC (my birthplace) I hope to see you, AC, and Gretchen Carlson. The short blond hair guy (the one from he Jimmy Dean commericials) and the one with the bad tupe would be fun to meet as well.

Janice

I’m a fan. My wife and I have always enjoyed your enthusiasm for the weather. Your a great part of the overall Fox News package.

I’ve taught martial arts for years, both the hard arts (karate) and the soft arts (t’ai chi). I’ve had the privelege of working with people living with MS. I’ve learned from them and have been pleased to help them work to improve their balance and strength.

I wish you all the best. Your attitude couldn’t be better.
Jim

Janice,

A friend in the television production business forwarded your blog to me and I was shocked and saddened at the news.

You see and hear of things like this happening to “other” people, but never someone you know. As a friend and former co-worker I want you to know how special you have always been to me. Although we may not talk as often as I think of you, I’ve kept up with your career after you left Houston and am so proud of how far you have come in this sometimes cruel business.

I hope we’ll be able to see each other again soon so I can give you a great big hug and kiss and tell you again, “I love you.”

We’re all saying our prayers down here for you.

Sincerely,
Don Armstrong
Traffic Reporter
SkyFox
Fox 26 Houston

Janice-
My mom has been diagnosed for over 23 years. While my mother will probably never live to see a cure, I appreciate that you have used your celebrity to highlight this worthy cause. I empathize with your struggles, and it does give my mother some solace to see that this disease knows no boundries when it comes to fame, wealth or station in life.
Good luck to you, and God Bless you.

Janice Dean,

You are such a real person on air and apparently off. I applaud you for your honesty and sharing of your challenge. I have always been inspired Neil Cavuto’s approach to dealing publicly with his MS. I expect no less from a wonderful person such as you.

Courage!

John

Janice,

You have been part of our family for quite a while. You are very brave for opening up and sharing your story. God bless you. Prayers for continued strength and courage. Keep up the great work.

dw

janice,

thanks for your openess. I think as more people are willing to share their roads, we will all benefit.

You and your husband will be in my thoughts and prayers. Best Wishes.

Jane

Janice,

Thank you for sharing your illness with us. God bless you and keep you.
You are a very brave and courageous woman, even when you don’t feel like one.
You will always be in my prayers and thoughts.

Thank you for sharing your story….I have a friend that has M.S. and she will be encouraged by your positive attitude. You are a strong lady….

Janice, as someone who also has been diagnosed with RRMS, I was so glad to see your story. I had just gotten back from my 6 month neurology visit, and my dear husband had saved your story on line for me to read. I am selectively telling people I know about this disease and that I have it. I cried reading your post because you have mirrored my feelings with how you are processing your diagnosis in your own mind. It’s terrifying and intriguing at the same time! Thank you again! It may help take the fear and stigma of being wheelchair bound to others who don’t know much about MS (yet!).

Janice Dean,

Your are great and I love it when you make a move, dance that is. I’m sorry to hear about your illness. Take courage: one day all illness will be done away with, Rev 21:3,4 and Isa.33:24.

I truly enjoy you and your weather report, hang in there.

Horace

ATTN: Bill21782

Hope you come back to read this thread….To get to video clips go to

http://www.foxnews.com/video/index.html

Then “Top Video by Section”

Then “Fox Fan”

There are a few clips there of Janice dancing

Janice,
I admire you courage to be so open with millions of people. You are truly a role model to us on how to live for the moment. As the song goes- “…life is a journey, not of destination.” Best wishes to you and your family. I have a feeling your family just grew exponentially!

Karri O.
Barboursville, VA

Hey Janice, I went into your blog because I saw you recently with a big ol’ diamond on and wanted to say hey, you go girl, didn’t expect the MS thing… but, God Love ya (as my grandma would say), you have a great outlook on life… sometimes the curve balls that life deals you, just make you a better, stronger person… stay positive and life will be good.. I’ve been experiencing my own “curve balls”, but, as long as we keep our heads up and a smile on our faces.. it’s all good!
Kerry

Janice, you are one of the rare and real media sweethearts and one of the few I feel it would be worthwhile to meet in person.

Sorry for your illness, although I know this won’t keep you down. You’re a dandy. Best of wishes in all things.

Jim

Dear Janice,

Thank you for your courage. Thank you for sharing your struggle with MS and bringing attention to this health issue. Thank you for bringing joy and a smile to the Fox weather reports. I am more of an admirer now because in spite of the MS diagnoses, you continue to be wonderfully winsome and positive. You are an inspiration.

You have been one of my very favorite on-air personalities ever since the Julian “Kung-Fu” segment aired a year or two ago and you responded with your own version of the Kung-Fu dance. It was a great segment to showcase your great on-air personality!

You will be in my thoughts and prayers.

En Cristo,
eloy

Hello Janice-
thank you – thank you- thank you- for putting a face on MS that is known to the world via FOX News! Your video does a get job at explaining too – it gives those of us with MS whose faces are NOT so known a face and a voice!!
I appreciate it more then YOU know!
It sounds like you were diagnosed around the same time as me. I have beem fighting those pesky lesions since August 2005- and celebrated today kicking off MS Awareness Week by going to my MS doctor – hehe who happens to be from Canada like you (Dr. Dean Wingerchuk, with the Mayo Clinic).
He is down here in Scottsdale, Arizona now- where I currently live- (I am orginally from NJ as your co-worker Neil, I believe)
Don’t visit Phoenix in the summer, your MS will suffer for it! Well YOU know the weather here ..hehe
I also posted your story on my myspace and send massive e-mails to all my friends in honor of this Awareness week.
I will keep you in my prayers-
love and MS HUGS~
Jill

BRAVO Janice!

You are an inspiration to all, espicially to those of us who fight the good fight daily to battle the misconceptions people have about those of us who live with chronic conditions.

You are a CLASS ACT!

Hi Janice.

You never fail to make my day brighter when you are on my TV.
You always have a sweet smiling face when I need it
Although the weather might sometimes be gloomy you remind me
that it will be better tomorrow.

PS…. When you gonna do Redeye again?
You are the best guest ever! You make
me laugh with your silly (and sometimes
naughty!) comments

You are an incredible brave woman, to come tell all of us about this. Anything this Canadian OV guy can do, let me know.

I was saddened and moved by your story of having MS. I suffer from other autoimmune disorders as well. You have brightened the set of FOX News with your vibrant, joyous spirit and approachable personality. God bless you in your future!

Dear Janice,

You are a beautiful and brave person, first of all for sharing your diagnosis rather than hiding it. There are so many people who hear a diagnosis like that and it derails them. They lose their courage, they become dependant so easily. As long as you keep the faith, try to stay strong, and remain open about your disease process, many people will become aware, become less frightened of hearing about MS, and it may give them enough of a boost emotionally to stand up for their lives and keep on keeping on, as you dear lady.

God Bless you, and stay strong.
Rochelle R. Helton
Hermitage, MO

What made you check for MS? Medical indicators you had. Thanks and take care.

Dear Janice –

I am saddened to her about your struggle with MS. I have a birth defect, and am in a wheelchair. Like you, I am open about my disability, and believe public education is important!

Mark

Janice, We watch fox every morning. You always put a smile on our faces and in our hearts for a start to our day. We hope our prayers can put a smile in your heart ! KEEP ON DANCING !!!
The Buyea’s, Oneida, N.Y.

Dear Janice,
I am a big fan of yours, even more so after you wore your Giants blanket that one morning during your segment!!
Please take care of yourself. And please make sure you don’t ingest anything with aspartame artificial sweetener in it – it has produced MS-like symptoms in many people.
A fellow Giants fanatic (in Texas!),
Andrea

Janice, your a beautiful person inside and out…. you just keep plugging away,
and I’ll keep praying for you.

Keep smiling, your a great person

Janice,
I so admired your story on Sunday. I always enjoy your weather reports. I was a clset Mser for 8 yrs. diagnosed in 1995. It wasn’t until my right leg weakness started that I had to use a cane and now a walker due to balance issues. But hey, life does go on.
I will tell you that over the last 4-5 yrs I have facilatated a Self Help Group and it seems the people I meet diagnosed with MS have incredible life stories to share. I think what most of us want is to be known for who we are as a person and not that we have the dreaded disease.

It is good to put a face to the name and the fact that you are so well known helps people understand that this disease unfortunately has no boundaries. Remember that Attitude is everythng.
And speaking with others that have this disease can be very helpful.

Wish you all the best.

Carol

Janice…I’m sorry it has taken me this long to write you. My wife and I have had the opportunity to watch (and listen) to you through your career. As members of a viewing audience we rarely get to meet, or get to know, those whom we come to admire and even love in an abstract way. I hope one day that we will have that privilege.

As you are one of those who, in the media, get to touch people in an abstract and vicarious way, let me say that you have indeed made an lasting impression in both our lives. I remember when you were the only sane voice coming from the Imus Show…and how you dealt with his “pet name” for you on his crappy program. What a classy lady you were…and are! You are NOWHERE near what he referred to you as.

As for your latest situation…I am certain that you will deal with it with that same poise, character and beauty that you have handled your entire life. I do not offer you pity, you are too good for that. But, my wife and I will wish you well, say a prayer and thank FNC for the wisdom and the courage to allow you to be who you are, and support you through this trying time.

Next time we’re in the city, how’bout lunch? We LOVE Sardi’s!

Be well and blessed,
Bill & Sandy

Dear Ms Dean

I lost my wife to MS a couple of years ago, and I admire your openness and courage to air your personal life on TV. I listeen to Foxnews almost all of the time, i am partially blind and i cannot see the TV very well. You always come across as a cheerful and happy lady. Keep it up. Fox must be a good place to work because everyone seems to enjoy their jobs. I live in Alaska, could you give our weather sometimes, thanks

Well Janice, I admire your will and determination. I was diagnosed in 2002, six months after the birth of my son. I am in the media as well, no where near as big as you…only market #106 (ha ha) and just a Community Relations Director, however, I believe a positive attitude can make anything happen for anyone.

The Mellen Center at the Cleveland Clinic has helped me to live well with MS, my doctor is brilliant and with the injections, medications and meditation…I am making it.

Best wishes to you and thank you for being so brave.

Madonna Chism Pinkard

Dear Janice,

I have watch you every single day and have loved the way you do the news on Fox. I am so happy that you have share this for now I can pray for you along with Neil who is such a strong guy.

I have an old college friend (Biola-Norwalk,Ca.) Dianne Cedarholm we ended up living pretty close to each other when our children were young we have been best friends for years and one of her daughter just found out about two years ago that she has MS she had just gotten married to wonderful man and just gotten her second degree, but what a trooper she is and Janice she just gave birth two months ago his name is Andrew and the doctors tell her she can have one more if she does it fairly soon. You all who have MS are a real help to me just to endure my everyday problems. God Bless you for letting us know! Janice can you keep my e-mail and let me know how you are doing. Sincerely, Mrs. Beverly Fisher

Janice, my thoughts and prayers are with you. I was diagnosed with MS almost 7 years ago at age 54 and am still working over 50 hours a week at a very stressful job (Customer Service Manager in a worldwide manufacturing company). I’m convinced that it is all about attitude. You can let it consume you or you can fight. Stay strong, stay active and don’t give into this.

My best wishes,
Chris

Janice, My daughter was diagnosed with MS over 30 years ago. I thank the Good Lord that it was not the debiliating type that confined a person to a wheel chair and unable to do anything for themselves. With every dark cloud, there has to be some sliver of a silver lining! She’s had 2 son’s who are currently officers in the Navy. She is employed and does everything that “normal” people can do. Once in a while she will have a “spell” and not be able to do different things.
that really infuriates her. Normally, she is a very “normal” person. With the little bit I know about MS, I wish you the best of everything and continue doing what you want to do. Sending a Mom’s love to you and all the others with MS.
Kate

Hi Janice, My husband and I think you are wonderful. We enjoy watching you on the weather. We would like to see you do more news segments. We’ve seen you do several segments…but they need to allow you to do more.
Your segment on “Fox and Friends” about your health was very well done. I have a form of Muscular Dystrophy called Polymyositis, so I know what it is to live with daily pain. I figure if you are going to hurt sitting home on the couch….you might as well hurt while getting out there and doing something worthwhile.
Congratulations on your marriage Janice…to one of our hero Firefighters!! He must truly be a gem
of a guy for you to have chosen him to say YES to. May you have a zillion happy years ahead.
We have been married 38 years and my best advice is COMMUNICATION!! You can never talk too much to each other…you are each others Best Friend!! Do you plan on having children? None of my business…huh!!
Maybe you could help answer a couple questions for both my husband and I. Fox has two Reporters who we believe were Reporters here in Las Vegas at one of our local stations, KLAS TV-8, a CBS Station. The Reporters are, Trace Gallagher who does alot of Fox Reports for Shepard Smith. The other Reporter is Julie Kurtz who reports for Fox from Washington D.C. We sure would appreciate an answer to those two questions…we’ve been wondering about the two of them for months and months.
Again Janice, keep up the Great Work. Keep that Beautiful Smile and Bubbly Personality! We enjoy you so very much. Please give our regards to the “Fox and Friends” crew…Great Show and we look forward to watching it each morning. This is the first time I have ever written to a Personality..but just had to respond to your segment. God Bless You and Your “Mr. Firefighter”!!
We sure would be most appreciative of a reply about Trace & Julie, and we thank you in advance.
With Prayers, Pete & Bonnie Peters

How brave and wonderful for you to go public with this! I was diagnosed with MS in 1996. After many, many tests (you know about those!), doctor’s visits and physical therapy appointments (I couldn’t walk well at that time), I decided that I had MS but it didn’t have me. I am fortunate that my flareups don’t disrupt my life too very much. Most people who know me don’t even realize I have this. When those in the public eye go public with their personal issues like you’ve done, it helps to call attention to this disease. That can do nothing but bring positive attention, funding and research to MS. Thank you for your unselfish commitment to bringing attention to MS. You look as “normal” as I do each day when I watch you on Fox. You are a bright spot in the day. Good luck and I certainly wish you the best!

Thank you for the article. A co-worker sent it to me. I have Primary Progressive MS. Unfortunately, it is only 10-15% of the MS population and does not respond to injections and drugs that are currently helping many relapsing-remitting patients. If you know of anything or anyone who could help me and/or talk, I’d appreciate it. Thank you!

Joanne Bennetti

I think God gave us our trials so we may help others as you are doing by speaking out..i suffer bi polar and cancer and im 61 and im male…its hard to give in to the fear and the stuff that goes with any decease and it hurts everyone around us if we are sad and sick…glad you spoke out and i love ya for your courage. Keep up the good works and we shall get stronger together as a group im sure…..Thanks

Jancie, I feel for you. I have a cousin who live in Alaska who has MS. I saw her for the first time last summer and was really amazed. She is in a wheelchair now and needs help with everything. Despite her illness, she is the most happy-go-lucky person I know. You will be able to get through this…I know you can!

Julie Zimmerman
MN

Janice, may God continue to bless you and give you strength. I can really relate to how you are feeling. I have a disease similary to MS, I have CRPS (21years) and there is little known about it. Can you imagine that diagnosis and not having many avenues to turn to to get answers? There are no telethons, celebrity faces or campaigns for my disease. JUST PAIN.

Again, God bless you Janice, and stay strong. You have a very powerful avenue to share your story and raise awareness for MS, please continue to do so. I will continue to pray for you. I was shocked when I heard “not J. Dean the weather machine”. I watch you everyday. You are beautiful inside and out and I couldn’t even tell – You look GORGEOUS everyday.

Sincerely
Peace for Pain

God bless you Janice and give you strength. When those in the public eye go public with their personal issues like you’ve done, it helps to call attention to this disease. Best wishes to you and your family.

God bless you for writing about your illness. It reminds me of courage, class, and the understanding of the wonder of life in every minute of the day. I do not have you illness, yet I have had some very difficult times and I found you positive attitude inspiring. L.

Dear Janice,
I’m very sorry to hear about your MS. You have a terrible condition, but if anyone can go through it with grace, It is you. You are in my prayers. Keep laughing and God Bless.

Hello Janice: Thank you for your frank discussion about your MS. I don’t have the disease but I know several folks who do. Actually, I was shocked to “connect” MS with YOU! I love your weather reports with their banter & joking around. Just the other day I was thinking, “That woman really loves her job & her co-workers.” Thanks again for sharing…you are brave & intelligent & beautiful, inside & out!

just to let you know that we watch Fox news most days and we love to see you give the weather forecast. Also love your little ‘happy jiggle’ dance. From Dennis and Brenda in Torquay, Devo, UK.
p.s. wet and windy here.

MY PLACE OF EMPLOYMENT ONLY ALLOWS US TO WATCH TWO NEWS CHANNELS,FOX AND CNN,I CHOOSE FOX.SO I SEE YOU PRESENT THE WEATHER NATION WIDE EVERY DAY.TODAY IS THE FIRST TIME I SAW YOUR BLOG ON FOX. I ENJOY WATCHING YOU BECAUSE, YOU HAVE SPUNKY PERSONALLITY.WHEN I LEARNED OF YOUR ILLNESS, I WAS INSPIRED BY YOUR STRENTH AND WILL. NEIL WAS RIGHT ‘STRONGER AND BETTER PERSON’AND IN MY EYES YOUR NEW NICK NAME ‘SPUNKY’STAY STRONG AND GOD BLESS YOU. TODD

Janice,
I have watched you on television since you did the “Scum Report” on Imus in the morning. My daughter works with the MS Society in Denver and forwarded me the article about you have MS. Her boyfriend was diagnosed in October with MS. He is taking daily injections and is also doing fine. Until he was diagnosed, I thought everyone with MS had a death sentence, but I have learned a lot about it since October. I’m going to Denver in May for a Walk-a-Thon for MS. Thanks for sharing your story with us.

Janice,

You are a beautiful woman — Both inside and out.

And your positive attitude towards life and MS shows that you have already won.

Have a great day!
Best Regards,
William

Dear Janice,

I have always loved your personality, grace, charm and quick wit! I especially liked the occasional “couch time” on the weekend Fox and Friends. My thoughts and prayers will always be with you. You are special.

Gary

your a very brave lady, I would love to thank you for letting the world no this and for me also, I had cancer when I was twenty twi old, have been cancer free now for 25 yers, wow where did the time go!!!! it was and is very hard for me to tell peole I had lung cancer at one time, they look at you and do treet you alot diffrent. Enen the ladies I have dated in the past, I was scared to tell them for scaring them away but again thatn you so much

Dear Janice, you are by far the most lively person on Fox News. You seem so happy and care-free, that I would not have imagined this in a million years that you suffer from MS. I admire you for your courage and the ability to be so joyous, funny and cute while doing such a good job.
I pray that I, who suffers from fibromyalsia could possibly have just half of your ability to be so lively and couragous. A committed fan, Love, Judy Camp, South Caroina

You are a beautiful (inside and out), incredible woman! I shall hold you in my thoughts and prayers until they find a cure for you! (And I know they will!)

Keep the faith!
Jan

Dear Janice,
Thank you for your bravery! I was glancing through this book called “All Your health Questions Answered Naturally”, by Maureen Kennedy Salaman while simultaneously reading my Fox News. (I am aworking mother and have mastered multi-tasking) There is a chapter dedicated to MS. I read it. It might be worth a glance from you!! On the front cover of this book it reads, Others Tell YOu what you already know, This book will tell you what you need to know!!! I am looking for help for my husband, he is showing signs of a desease that is not readily recognized by doctors, or by tests. I am going to apply “the suggestions” made in this book to help him learn to live with this desease. Perhaps in a couple months I will email you with a successful update. Don’t rule out going “outside the medicine world”. I truly believe that God has made us perfect in his image, and the ability to find cures/remedys to maintain those images are written and studied by others who share that belief. Read it, it couldn’t hurt!! I will put you on my prayer list and hope that you will always maintain the attitude and positve outlook you have today!! God Bless, all my best, Cathy Hurt, NC

Dear Janice;

Our family just loves you! We are so sorry to hear about your illness. You are in our hearts and prayers and we wish you the very best as you fight this life altering disease. We so enjoy your forecasts and your wholesome quips, always so well delivered. We just wanted you to know that we appreciate your candidness and your willingness to help others who face this disease.

Our Love and Prayers

The Geitz Family

Thank you for sharing your story. You are a beautiful woman with a great future. I love watching you do the weather and it will mean more to me now that I know your story. Best of luck in your battle with this illness.
Love,
Beth

Janice,

I have been waitching FOXNEWS religiously here in South America the last 2 years I have lived here. I have always enjoyed your openess and energy – and the bathtub pic. You are a courageous woman. I wish you the best and know you will be a great spokesperson for MS.

Jacob

Medellin, Colombia

having listened to Janice over the years. Houston doing traffic,and being a radio DJ in Houston. I know janice will do her best to perservere. Her quirkyness one morning when one tal kradio host went on vacation and the station owner didn’t wake up in time. janice and other folks carried the morning. Best to you ,Janice.

Hi Janice. thanks for your blog. I think I’m about to be diagnosed with MS…an eye doctor diagnosed me yesterday with optic neuritis and today I had the MRI to look for leisions. I’m scared. I have no idea what to expect, but I’m so glad there are people out there like you to show us that this disease doesn’t have to be a death sentence. I would love to hear from you.
Most sincerely,
Erica Assimakopoulos
Niskayuna, NY

J.D.,
Thank you for your “blog.” I watch you along with Bill & Meg most every morning. You all are fantastic people. Thanx for sharing about your illness, we will keep you in our prayers for sure. Having lived with Alcertive Colits for 25+ years and now Fibermyalgia one can identify with you. Never give in to the doctors and always go forward in faith. You and Tony Snow etc., are shinning lights. Keep up the great work and that great smile on your face. Blessings. Rev. David J. Dunham – Minot, ND.

Janice,

My thoughts and prayers are with you! My company watches Fox religiously in our NOC and you are always a bright spot in our days, when I saw you have been diagnosed with MS, I felt the need to send you a note as I have been battling MS for over ten years. I was an Infantry Captain until 1998, when I was discharged I was diagnosed with MS. The only advice I can give is live your life the way you do now, I have run two marathons and planning on running a third in May. You can do anything even though you have MS. Just keep you chin up and stay healthy!!!

I also read Neil Cavuto’s book several years back and it is a great read for anyone battling an illness, I am sure you have probably already read it!

Janice,
My husband and I love watching you – you are brave and beautiful and here’s to many more dances! Thanks for making us smile and being such a class act. You are the best and we send our best wishes to you.

A co-worker was diagnosed 4 years ago and has coped very well with this disease.

May God Bless You Janice.

Carmen

Janice, I just read your blog and was very touched. My mother-in-law had chronic MS since 1964 and passed away 42 years later at the age of 82. She led a full life and it was only in her last years that her MS took its toll. Other than B-12 shots she really didn’t have any other medical input. Stay active, rest when you need it and smile that beautiful smile. God speed.

Jeanne

Janice I was shocked and then amazed at your story. You are beautiful and you bring so much needed humor to the news and weather. I crack up at your weather segments. A friend and teacher here in Selma, Alabama was just diagnosed with MS and she also young and attractive and like you will not let it effect her attitude toward life. You are in our thoughts and prayers and please keep us laughing.

Janice,

I never knew, but then how would I know. I donlt have MS but I know people who do. I never really understood clearly exactly what MS was. Now I do. I never realized that I “might” have it myself…. it’s time for me to get checked out. The bottom of my feet comment you made has me concerned.
At any rate, you are a wonderful person on air doing the weather, and a champion for sharing your condition. No wonder Fox does so well, their employees are human, real, compassionate people.
The thing that touched me most was the way you sigend your blog. “Love, Janice. You are talking to millions of people that you donlt knwo and could never meet but you sent your love and I “know” you meant it. Thanks for the class, style, and humanity that you are! Best wishes to you,
Love, Jeff

Dear Janice Dean (our most Fabulous Weather Machine) -
Thank you so much for letting us, your viewing public, learn just a little bit more about what a truly awesome person you are. I’ve read about “Neil’s” challenge and how he views life. We now have one more crusader whom to learn from!

God Bless you Janice!
Jeff Fulton
Flower Mound, TX

Janice,

Your openness and bravery in the face of adversity is an inspiration.

I’m a veteran of the Persian Gulf War (DESERT SHIELD/DESERT STORM), now jokingly referred to as Gulf War I. Anyway, we had a saying we resurrected from our Vietnam War brothers and sisters,

“For those who have fought for it, life has a flavor the sheltered will never experience.”

God Bless you and your family.

Janice;

I am very sorry you have

Thank you so much for sharing this. I had no idea. You are my favorite weather person and I think we are so blessed to have you helping us plan our days! Love and prayers,

Rita Cantrell
Homewood, Alabama

I still miss you on Imus but am always happy to see you on Fox. Good luck and keep your great attitude.

Janice;

I am sorry to hear you have MS, but you are a very lucky lady to have friends who love you and are pulling for you.

Please continue in good thoughts while they find new cures for your decease. You are very resourceful lady and don’t let this get you down.

I love you on Fox as the weather person. You are a very good at what you do. Keep up the good work.

May G-D bless you and keep your chin up.

Pamela
Pensacola, FL

Thank you for sharing some of the details of your illness; the informatin is very inspirational. My friend’s daughter has MS and I pray for her often. I will include you in my prayers.

JD,

You Rock!!! My sister was diagnosed with MS officail at the age of 16 they actually think she had it at 3yrs old. Be thankful for the wonderful life you have and your ability to function at the level you can. Its a true gift. Your wonderful personalitly and caring ways shine thru even on bad days. Thank you for sharing this painful part of your life with the public. Please always know that their are others that live, laugh, love and suffer with you:-)

Janice,
We are sorry to hear about your MS results. Keep your chin up! I’m laid up with a bad back injury. I have damaged nerves in my lower back and recently had a neuro-stimulator implanted just recently. I haven’t smiled much lately. When I watch FOX news(all the time), I love it when you give the weather report. We never know what we are going to get from you. You make me smile EVERY time! Thank you for being you!!! Don’t you ever change!!! We will pray for you!
Love, Terry Ackley, Vestal, NY

I just want to say That I know the journey as well. I was diagnosed with MS in Feb. 2005 and like you I’m sure I had it years ealier. My wife of six years is divorcing me now because she does not want to deal with it. She is a nurse(go figure). I still work and function as close to normal as I can. Thanks for sharing your story. I don’t know anyone else personally that has MS, so it helps when people you see on TV let you know its OK and you are not alone…I am 49 yrs old and hope I am around a long time…

A friend of Fox
Carl

Janice,
I’ve been a fan since you were doing traffic on the radio in Houston!

The Houston to Austin MS150 bicycle ride is coming up April 12th & 13th. Last year, the 12,000+ cyclists raised over $13,000,000. This year, we’re working for even more. Please know I and my 40 member team (Clear Lake Cyclists for Christ) will be riding in your honor.

Thank you for being an inspiration to the thousands of Texans who live with MS. Stay strong!

Janice,
I wish you the best, and thanks for going public with your illness for others in the home audience who are suffering from MS or some other debilitating disease.
You are a joy to watch on FOX — I enjoy your personality that you project when reporting the weather. When there are dangerous storms on the radar, you show an honest concern for all those in its path. You seem to be a kind and caring person.

Many prayers are being said for you.
Becky

Janice,

Thank you for sharing your story.

You always brighten my day with your smile and I enjoy your sense of humor.

My wife and I will be praying for you. Trust God, He will give you the strength you need to see your way through this.

Ken

Hi Janice

I just came in and your segment was on and I caught the tail end of it. I’m really sad that you are going through all that. But Jan it does not have to be that way. I do not have a degree or wear a white coat so you ( do you have good days better then some )
will just have to take my word for it. When you started having these symtoms you went to the Doctor , did he or she take x- rays ? you told them your symtoms they probly found some Demelination or lesians which are nerves which send messages from the brain to the muscles.They
get so excited they die thus the lesians appear on x-rays. Stay away from anything Diet or better yet read eat all Organic food. Read labels carefully. MSG ( it’s in everything ) Breaks the brain barrier that is suppose to protect all of us. It is an Excitotoxin as is Aspartame it is Toxic ! Peoples lives are being destroyed for money, how does it get in there by accident, I don’t think so.You are so beautiful. And it breaks my heart to hear of you with a unnecessary illness. Don’t ask your Doctor, Do you think he or she will go against all they have been taught.I will Pray for you.Take care of yourself

Janice,

You are a delight to watch, one would never know you were dealing with this in your personal life. This must be very scary to have MS and to go public with that. I admire your courage and will be praying for you.

God Bless you.

Dale

Keep Dancin’

God Bless

Bill

Janice,First off congrads on your wedding,I just knew you were a “Hot Babe” lol I watch Fox every
day being retired for a year or so. I always enjoy your part of the program ,as it injects some humor in my AM here in Oregon (HighDesert) by the way its great here this PM sunny mid-50,s
just a little weather report…Thanks for being up front about your illness,I wish you all the best w/
your health and hope for the cure…God Bless

Janice,
You have alot of courage to share your life with others. Most people would hid something so revealing. I just want to encourage you not to lose courage when you feel less than courageous. Knowing many wonderful people who has MS they live happy productive lives. Your “bubbily” personality is essential to living with MS and encouraging others that life doesn’t stop at the water’s edge.

Blessing unto you Janice

Curtis

Janice,

I seldom have the opportunity to watch you give the weather news on tv; and honestly, the newspaper or radio news is usually enough for me. Even now, seeing your smiling face on the internet, i was drawn by your image and personality, rather than a desire to know the news.

I liked you before i knew that you had the courage and generosity of spirit to go public about your disease. I didn’t even know that you are married. Your husband is a very lucky man. The rest of us are fortunate to benefit from your inspiration.

Best of luck in all things,

Peter

janice,

you will always be janice dean the ‘weather machine’. your personality and charm always brightens the screen. just remember to live through your strengths – not your weaknesses.

god bless you! keep on dancin’

ken
lexington, kentucky

Dear Janice,

I was so moved when I read your blog. You are truly an inspiration to us all. God bless you and keep you safe and well. You are in my prayers.

Keep on dancin’

Pat Harper
Pittsburgh PA

Dear Janice,

I watch you all the time on Fox and I am amazed at your incredible energy. You smile is so uplifting and I don’t think anyone would have thought that you had this disease. I am so sorry this has happened to you but there is hope. I know something about that.

On May 27th, 1993 a little boy named Nigel Ian was born to us. He gave something to my life that
wasn’t there. I was frightened yet filled with joy at the same time. All he ever did was smile and
laugh. He never cried, he never was a problem he was the Perfect child. At a little over two and a
half years old we found out what was wrong with this perfect child. Nigel was autistic. I was crushed. I had so many hopes and dreams for this child and those dreams would now go unfulfilled. I vowed never to give up on this little gift from God. He uttered his first word at four and I knew it was going to be a long road. How little did I know what a triumphant road it would be.

Today, Nigel is nearing 15 years old and not only can he speak, he can speak in two languages, can dress himself, cook for himself and do almost all the things that children not afflicted with a
disease can do. I have said many times that Nigel has given my life great purpose and Adriana
(daughter) has been the love of my life. They both were there on August 26th of 2006 when I fell
off the house and almost died in the driveway. The point is it is not what we have to deal with, it
is how we deal with it. I saw another comment that stated you need to control MS, not have MS
control you. I couldn’t agree more.

I think you are a very brave lady for sharing this with all of those who already thought of you as
grand. I wish you God’s speed, peace and hope. For hope is what gets us through to another day.

Be well Janice, you are in are thoughts and prayers.

Edward, Nigel and Adriana Broderick

My Daughter was diagnosed with MS about 3 years ago. She worked as a postal clerk and began with double vision. When she went to the doctor they did an MRI , gave her treatment in the hospital for MS. She was asked at the post office to apply for her disability, She was beginning 20th year. She’s only had one episode since then and is faithful to take her shot daily and working part time as a checker at a grocery store and loves being in the thick of things without all the stress she had at the post office.

She sees now that the constant stress was a factor in her MS, it may not cause MS but it can kill you if you keep it. She was lucky to have it wait to appear until she was 50, some people get it as a child.

Our MS Support Group went to a meeting with a Dr who has MS from Hot Springs, Arkansas told that there has been people with MS since the Fourteenth Century, But practically all the research has been done since l990. WE’VE COME A LONG WAY BABY! Good Luck, life is what your attitude is, so keep smiling. Nelda Parrish Corinth, Ms. 38834

Janice.
I will say a prayer for you as often as I can remember to – I love your attitude , your energy, your personality…you have made watching the weather much more interesting to say the least.
I don’t have MS but I know what it like to have your future change in an instant – I lost my hand in a saw mill accident at age 16 – as a jock and someone who desired a career in the military I thought life was over and unfair while I was in the hospital recovering – 41 years later I look back and realize it was just another challenge of life, some of us have more challenges than others but always keep that pretty smile of yours it makes the day for a lot of people and I’m sure your husband is one of them.

God bless….

I’m a 43 year old mother of 3 daughters who also suffers with MS. I was diagnosed 5 years ago when my youngest daughter was 15 months old. My doctors and I feel I have had it a long time before my diagnosis probably in my teens. I am no longer able to work as I am confined to a wheelchair and need help with daily living. I am very fortunate to have a fantastic support system. MS has opened my eyes to the good in people. It has also taught me to tell those we love how important they are to us.
MS is not a death sentence but it is certainly life altering. I love being a mother and being able to be in my children’s lives. I’m still their mom even in my wheelchair.

my daughter was diagnosed with MS at the tender age of 19. she is 27 now ( 28 on 4/4). she has been so brave throughout this illness. to tell you the truth, i’ve learned a lot about life and whats important too. the road has’t been easy for my daughter, but she has never let this disease stop her from doing what she wants…………….even at my urging to sit down and rest sometimes! I’ve just learned to just watch and enjoy her have a fullfilling life. She has been an inspiration to those who know her, showing that MS doesn’t have to get you down. if you ever need an inspiring story, she is the one, always helping others even when she does’t feel well herself.still won’t sit down! she has a great support system.her 10 year old son is so helpful and understanding when she doesn’t feel up to par. well god bless you all and .we know the journey too.

This is just for Janice.

Dear Janice,

I never realized how beautiful you are until today. I’ve never been a fan of weather shows, to me
weather is just something that’s going to be there. Sometimes it’s going to be hot, sometime cold,
sometimes wet, and sometimes dry, and sometimes it’s one when it’s supposed to be the other, so what, it’s all good, no matter what.

But from today on, I’m a “Janice Dean Weather Fan” because for me it will be forever beautiful where you are.

God love you.

Joel

Dear Janice,

May GOD bless you!!! Always look to Him for strength and direction. After all, GOD is the master physician. I get the feeling that you know that already. I will pray for you and your family, Janice.
God Bless,
Keith
A fox news fan.

Hi Janice,

Your bio sounds familar, I too have MS & 9 years ago my daughter was dx with MS also.
I’m sure you have heard the phrase “but you look so normal”, guess what—we are,
“just alittle hitch in our get along”!!! lol

If you don’t mind me asking, what therapy do you use?

Love,

Jeannie

Janice,

You are a bright and shinning star in the mist of the darkeness that is called life. Remember keep on smiling keep on laughing and continue to be a voice of reason in this difficult time that we live in.

As you go through your ups and downs remember this…

Faith sees the invisible,believes the incredible and receives the impossible.
With God all things are possible.

We will continue to pray for you and your family.
Rev.
Michael Risden

Hi Janice!
As my favorite weaehr personality on television, I was saddened to hear about the battle you are waging with MS. I just discovered this today as I was looking through the FOX blogs–so I hope I’m not too late to send my best wishes to you for a good fight! You are an incredible weatehr forecaser–I always appreciate the interaction with you and Shepard Smith when you’re on Studio B. I live in Hong Kong now, so it is hard to watch you all the time, but I’m still a big fan of FOX and the people who are on it!
If you ever need a listening ear or want to drop a line, feel free. I’m sure you are overwhelmed with offers, but I make it to you anyway!
God bless!
Jaden

I, too, have MS. I was diagnosed in Oct 2006 after having”Strange” symptoms for 6 years.
I am now taking Tysabri and it, along with prayer, has turned me around!! Diet and exercise are also playing a mjor role in better health.
I have formed a Walk MS team in Atlanta, Ga and I am asking you for clear skies with warm temperatures!! http://www.nationalmssociety.org/goto/dawnstone.atlanta

Keep the faith and trust God in every decision you make.

Thanks Janice for your blog. I related to so many things you’ve lived through.
I’m not quite brave enough to try any more treatments. I’m sure when I have a scary epispode I’ll change my mind. Back in 2002 when they diagnosed me they had me try 3 or 4 different injections. I either slept all the time or became terribly suicidal, one of the side effects “oh my gosh”. So I just stopped all of it and suffered the side effects of stopping which were much better than the side effects of the drug.
That’s why I’m a little afraid to try again. But I’m doing well. My biggest things are not being able to think of words, being very forgetful and feeling tired. My kids think this is just how I am.
Yesterday I was offered a job as an assistant for a fancy photographer. I pray to God that he was serious. The first job in about 25 years other than being a mom. I was so flattered and so excited!
Sorry, I just had to tell someone.
Thanks Janice for your story.
Dana

The story of Janice Deans opening up and sharing her MS diagnosis was sent to me from one of my customers. I was recently diagnosed in December of 07 with MS. It progressed very fast and I am currently on a Chemo drug called Novantrone (used for very progressive cases of MS). I was devistated when I was diagnosed. It has changed my life as it does with anyone. I have had wonderful support from Family and Friends and has helped me maintain a positive attitude.

I am on the next phase now, I call it a “Mission”. I have heard so many stories of people with MS in denial. I want to be there to help them in any way possible. This Disease does not have to ruin your life and keep you from happiness, it just changes direction a bit. I have always felt that challenges in ones life can make you a stroner person.

Through all my research and reading of MS, I have a clear understanding of what I have to do. I would challenge everyone to learn about this disease and other ones out there that there is no cure for yet.

Research is the key to finding a cure. I will be walking on April 12th for MS through our local chapter. It will be a major hurdle for me because of physical limitations but I can and will do it. In addition, my Team of Ladies and myself are getting as many donations as possible to find a cure.

If anyone reads this that is struggling with MS, it’s okay. We can all overcome the challenges of this disease, it can’t beat us unless we let it.

Hey
I see you have been through some tough times with this MS issue you are having. I love your weather show and think you are one beautiful woman and think there is a solution to MS. I believe if you take 1000 mg of magnesium and 500 mg of calcium per day you will see a difference. I have read alot on magnesium and believe that the lack of it in our daily dietary needs are whats causing many people with MS to suffer needlessly. If the New England journal of medicine says it a cure for cancer then its has to be good for something. If anything just look up the health benifits of magnisuim. Just cut and paste the following and read for your self. Magniesium health benifits testimonials.
I am no doctor nor do I have MS but read many articles on the web and have tried this myself for other related issues and found it to be very beneficial .

JANICE,
I WANTED TO SAY THANK YOU. THANK YOU FOR MAKING YOUR BATTLE PUBLIC. MY HUSBAND HAS MS AND WE HAVE SEEN FIRST HAND THAT NOT ENOUGH PEOPLE UNDERSTAND WHAT A PERSON GOES THROUGH. I TOOK MY HUSBAND TO RENEW HIS DRIVERS LISCENSE ALMOST 2 YEARS AGO. THEY REFUSED HIM BECAUSE THEY CLAIMED HE WAS DRUNK!!! HE WASN’T DRUNK. HE HAS MS. HIS SPEECH IS SLURRED….HIS EYES WORK OK, BUT NOT TOGETHER. BRIGHT LIGHTS BOTHER HIM, HE HAS TROUBLE MAINTAINING HIS BALANCE SOMETIMES. I’M SO GLAD THAT YOU ARE SHARING THIS WITH PEOPLE. MAYBE THEY WILL PAY ATTENTION AND NOT BE SO QUICK TO JUDGE THE NEXT PERSON WHO WALKS INTO THEIR OFFICE OR BUSINESS OR WHATEVER.
MY HUSBAND’S INCIDENT AT THE DMV WAS NOT THE FIRST TIME HE HAD BEEN ACCUSED OF BEING DRUNK BECAUSE OF HIS MS. HE’S ACTUALLY BEEN ASKED TO LEAVE SHOPPING MALLS, STORES, AND EVEN GOVERNMENT BUILDINGS. HIS BROTHER HAS MS TOO AND WAS ALSO ASKED TO LEAVE THESE PLACES.

THANKS FOR LISTENING AND THANKS FOR GETTING THE CORRECT INFORMATION TO THE PUBLIC. THEY NEED TO KNOW.

SENDING YOU MY BEST WISHES FOR GOOD HEALTH AND SUCCESS I YOUR BATTLE WITH MS!!

MISTY SHELBY
LINWOOD, NC

Bravo to you, Nancy, for “going public” with your diagnosis. The more “famous” people we have as advocates for MS, the greater the awareness and the sooner a cure might be found. I have been living with MS all my adult life but was not diagnosed until 1990 (I was 45). I jokingly said I was glad I didn’t know what was wrong with me because if I had known, I might not have done all the things in my life that I did! Just last year I submitted to treatment. I wish I had started treatment sooner as all the research shows that treatment does indeed curtail the progress of this silent disease. Betaseron injections every other day and IVIG treatments once per month are helping me. Good luck and stay positive.

Suzanne Nordstrom
Denver, CO

Janice,
I was diagnosed with MS 19 years ago. Although I am no longer able to work, (dental hygienist), I am still able to get aroung with the help of a walker or cane. I really appreciate your openess and honesty. Hang in there, take your medication and keep that positive attitude. I try to do the same, but there are times I get so frustrated because I can’t do things I used to! I think that is a normal reaction. I get over it and try to be thankful for what I can do.
I enjoy watching you on FOX. Keep up the good work!

Danna Street
Laughlin, NV

Dear Janice
I read today of your MS diagnosis-gosh I know how you feel as I was diagnosed in 1998, with symptoms going back another few years.
I have just retired from practicing and teaching dentistry for 42 years. I continued to practice for 10 years after being diagnosed, so don’t feel you have to give up the wonderful job you do for Fox. As a matter of fact, you’re the BEST at your job of anyone I have seen!
If I could give you any advice-my wife says I am good at doing that when not sought after-it would be to stay active! Exercise, excercise, and more exercise. But, not to the point of exhaustion or sweating, as that caused your core temperature to rise and thus works against your MS. Study all you can about nutrition and MS. The more you can learn about this disease the better.
Good luck and keep up the dancing! Call on the many resources you have to ask for information, including me.
Jim

Hey girl… I hope you remember me from Metro here in Houston.
The Chronicle did a story on you this morning, and I was saddened to read of your bout with MS, but heartened that you are doing ok with it. I hope your flare-ups are few and far between.
I’m sure you have heard by now that your old “buddy” Jon Matthews got what he deserved, and is probably sitting in his cell right now reading your article.
We do watch you when flipping to Fox and you look gorgeous. Congratulations on your marriage too! Keep up the good work.
I still maintain communication with Moss, Darby and Roger. Darby and Roger are still with Metro, but Moss and I have moved on. Hang in there!
Jim

Thanks for this article. I was diagnosed with MS in 2001, although one neurologist remarked that I’ve probably had the disease since 1980, when I was hospitalized with a paralysis, that was thought to be Guillian-Barre or psychosomatic.

Since my official diagnosis I’ve been compelled to retire from my job and relocate from an city which I loved, leaving my friends behind.

Ms. Dean has the ability to make the general public aware of MS, and I sincerely hope she can use her capacity as a TV personality to advocate for improved services for those of us who feel as if we have lost everything.

I was shocked when I read the news in today’s Houston Chronicle. I know of others who have also been affected. Stay in there, girl, and fight. All of us here in Houston have you in our prayers.

Hi Janice,
I read the article in Houston Chronicle about your diagnosis with MS. I was diagnosed a little over a year ago. Daily injections have helped a lot..It will be two years June since last relapse. It took awhile to diagnose after first relapse. I had the opporunity recently to hear Wendy Booker,mountain climber and marathon runner with MS talk about her expeditions and how each of us with MS have a “mountain to climb”. My “mountain”has been to continue to work and be successful in real estate sales. I had a great 07,but 06 was rough..hard to sell from inside the MRI machine and being fatigued! I’m feeling great now and am thank-ful for the new treatments available. Also grateful for having supportive husband and family.Thanks for being open about having MS. I have found it scary to reveal to others..some have judged and tried to use against me, but most are very supportive. Having MS has made me stronger..I don’t sweat the small things anymore!
I love Fox news and enjoy seeing you and Neil Cavuto on Fox. I bought Neil’s book right after I was diagnosed.I think while it must be hard to be in limelight with this disease you are a beacon to others with MS to keep plugging away. I figure if Wendy can climb mountains and you all can be on TV.. then I can still sell houses and be involved in my family’s activities. We’re going hiking in Big Bend this week! Embrace the moment! Best of luck to you..

Dearest Janice,
I’m not sure how many of these posts you will read, you have gotten so many from wonderful well wishers, isn’t that just “Fabulous”!!! Like everyone else here, I’ve seen your segment and I’m sure it took alot of strength to put yourself out there the way you did….I say, Good For You! Being able to “say it out loud” and not feel you had to hide behind your disease is a huge step in dealing with an illness. Finding our strength after being Dx. with M.S. (yes, I, too was dx. with RR M.S. in 99) is sometimes pretty amazing, but…it’s there, it’s always there! I have been fortunate enough to have found mine as well, and its been a pretty incredible journey, I must say! I’m doing well since starting on http://www.lowdosenaltrexone.org. I’ve been on it for 6 yrs. now and have’nt gone into a relapse since, not saying I don’t have “my days”! I tried all the shots (I was the ABC Queen) but found they weren’t working for me. Now, I take one pill each nite and Life is Good!! I was wondering what therapy you’ve chosen and how its working for you.
One peice of advice I give from the bottom of my heart is to Stay Positive Always! You said that you know how Stress effects us, it does…I kinda like having a fairly “stress-free” attitude, its worken for me!!
Life changes, but I’ve learned to pace myself, so I have the energy to put into things I love doing (instead of worrying more about getting the laundry done!!) Appreciate Every day, Love more, Laugh as much as possible, Give what I can, and Thank God Each and Every day for my feet hitting the floor in the morning!
Seeing the strength you have, I know you’ll do well. Always remember:
“A Healthy Mind makes for a Healthy Body”, and always Take care of your body!
God Bless you Janice. I’m here if you ever need someone to talk to. Lord knows I have some experience!!

Carol D. from NY

Hi Janice,

I just read your article today and all the best to you! I was diagnosed with MS back in December of 2004. I was diagnosed with optic neuritus. I saw double when I went to the movies with my husband. I was pregnant, so I couldn’t do an MRI to determine the issues I was having. They were guessing a pinched nerve, etc. I had a miscarriage and I did the MRI and they finally determined that I had MS. I immediately started the injections. My husband and I went on vacation and I got pregnant in 2006. We gave birth to a cute baby boy on 12/16/06. He’s happy and healthy and I dealt with flareups, etc, etc. I’m on a new medication/injection now and I am feeling well. Thank goodness! We will participate in the MS Walk in San Francisco in May!

You have all my love and support from the West Coast and I wish you the best. You’re an exceptional newscast person. Stay positive, take good care of yourself. take time to rest and have fun! =)

All the best! Rona from CALIF.

god bless you janice thank god for medicine in america they may have a cure soon

Janice, MS was DXed in 1987. Was fine and normal for 10 years, then started down hill. Speech was slurred like drunk. My oncologist who was administering Novantrone(chemo) told me of a new TX he believed in. Went for the idea rather than face wheelchair.
He gave me “cytoxin” over 4 days, reducing my white count to 0.0. Then over the next 2 weeks my counts came back to normal, with the help of various meds. My immune system was a blank slate — forgetting that I had MS !! Got chicken pox again whithin the first 2 weeks. But other than that, have been steadily getting stronger.
My DR was Douglas Gladstone at Stony Brook Hospital in Stony Brook, New York. (631) 444-4000.
It is chemo, and did lose my hair for a while. Cytoxin has been being administered for over 20 years, so the side effects are well known and compenstated for. Chance of death, 1 in 200.
Good luck and love your show, especially your Friday dance.

Kevin

Thank you Jancie for sharing this. I have a disease that I am still not comfy sharing so I can relate to your hesitance ~ One thing Ive discovered is we all have health issues…..yours is MS…mine is …( I still cant say it), others have diabetes, thyroid issues, HIV, heart conditions and so on ~ One thing for sure, MS hasnt stopped your great dance moves !!

Janice: We have something in common: MULTIPLE SCLEROSIS (MS). However, physically speaking, you are in better shape than I . You have relapsing/remitting MS and mine is secondary/progressive. But, THERE IS HOPE! There are nutritional science products, that I am taking, made by MANNATECH, an international company located in Coppell, Texas. PLEASE go to their web site (Mannatech.com) and read.

Mannatech has helped people overcome MS and they are now leading a normal life. It is not labelled a miracle cure because it takes time to replace the “sugars” the body is missing. I can send a DVD that explains it in detail.

This is NOT to replace any medication or treatment you are now receiving. These nutrients are just a dietary supplement. Both you and Neil should give this serious consideration. Next month marks my one year anniversary with Mannatech.

Kindest regards,
Paul Lupo
Watertown, SD

Janice,
Thanks so much for sharing your journey with MS. My sister has lived with MS now for over 15 years and she is such an encouragement to me. You are such a hero to me, to share your life with such openness. I love to wake up to your weather reports here in California!
You are a breath of fresh air!

Dear Janice, My Sister in MS
I was diagnosed in 1990. I am now 51 years old and still walking around. Congrats on telling your fans about MS. If we share our experiences, we will remove all the unknowns and the fears of those who come after us. At first, I thought it was a death sentence. After educating myself, and I am still doing that, I was relieved to know I could make it. Now it’s all about you, and you know what I mean. I retired in 1993, after realizing my type A job and type A personality was going to do me in. MS is a life changing experience. Make the changes good…..
You go girl
Mitch Thurmer

Janice,

While attending my local watering hole for a wee bit of St Patrick’s cheer we were engulfed by a small army of people wearin’ the green and collecting for MS.

Thinking of you I contributed a five dollar bill.

Just wanted to let you know.

Dear Janice, I have been meaning to write after your report. I was shocked that the fun, bubbly, beautiful woman who makes me laugh, was dealing with a horrible autoimmune disease. There were times your craziness made me think of myself. Then you revealed your MS.

You see, I am 42 and disabled due to Rhuematoid Arthritis and Lupus. I have what is called Combined Connective Tissue Disease.

I have your personality to a TEE!!! I have made the reason for living, LIVING.

After a wonderful job at one of the Big Three in Michigan, I was blessed to have one little boy, after 4 miscarriages. Then the Lupus was shown in blood work. In bed on injections twice a day, but so worth it, I had my beautiful little boy. He then had open heart surgery and continues to have a heart condition. Then the RA developed horrible. But, I was able to have my boy, and he is the personality of his Mom, fun, love, caring. He is my ROCK.

Then after being told no more children, I adopted my little girl from Moscow. I wanted to help a child, and still had enough love, even if days I cannot walk to bring this girl a different life.

They are both in school and I am still, hard some days, very very active in their school lives.
When they are in school, I rest now. I had help getting them to school age, but wouldn’t have done it differently.

These diseases are more common then ever and woman like you are the inspiration we need. We all need to still have love, life, laugh and fun. The only difference, we may not do it as long, fast, or from a wheelchair. But, with inspirational stories like yours maybe we can get a few woman to put a little makeup on and drive the cart around Target just to get out of the house, have a coffee, meet a friend, live with these horrible diseases.

As I watched you with tearful eyes, I knew I had to let you know what your story meant. I am a Fox News junkie, and when people ask, I tell them, the people on the channed make me laugh. I sit in my big old Lazy Boy, coffee, do my make up, dry my hair, and start the day. The day may be sitting in the chair watching all day, but I try to do something to make myself feel good.

Thanks to you and everyone at Fox. You do more than tell the news. You aren’t only the TV, you are fun and a reason to be!

Take care of yourself. Try to rest. Most important, love up your hubby and have FUN! Keep making people laugh.

(Watch it on those snow angels honey!
Lots of blessings,
Patricia Greenwald

Dear Janice,

That was a very good article about you and MS. I want you to know you are a fantastic weather reporter on TV so sweet and kind. I can’t ever remember a weather reporter that I remembered a name, or even cared until you came along and I’m 65 smile.

I didn’t see those photo’s of your wedding or you without makeup but I’m so happy you found a mate someone to love and to love you.

Keep up the good work and know we all love you and are waiting to get the real weather report from YOU.

Evelyn in AZ

Janice,
As a member of the U.S. Army, I have seen my share of heroes. We have all heard that heroes aren’t made, they are born. We jokingly say that heroes aren’t made, they are cornered. You are one of those who were born. I was watching the morning you disclosed your illness. I was very proud of you and I am still very proud. You are a fantastic person and a wonderful news woman. I have always enjoyed FOX and still rely on them for accurate information.
Keep up the good work and God bless you.
Wayne

Janice,

God bless You for Your wonderful courage telling us. You always make the sun shine here no matter what .
Charles.TX

Hi Janice:

But you don’t look sick! That one really gets old!!!!

Just read your blog and while I don’t have MS my soul mate of over 40 years does. She was diagnosed six years ago.

Outlook is very important and her positive attitude has gone a long way in helping us both deal with this life changing disease.

You might be interested in reading “Fall Down Laughing” by David Lander. (Squiggy). His battle with MS during the the Lavergne and Shirly show is classic for the time. David does a lot of appeareances on behalf of the MS Society.

Thoughts and prayers are with you and your family.

Tom Lenart

Thanks for going public as it has helped people I know you probably realize this however,

Hi Janice,
I’ve caught your bubbly weather forecasting and would never have guessed your secret until my husband told me tonight.

With the week of March 10th being MS Awareness Week, I’m so glad you chose to tell your story. You, and many like you (Neil Cavuto, Richard Cohen, Annette Funicello [every teenage boy's heart throb of the Mousekateers] and others) help to keep us inspired.

Like Mitch (after I was diagnosed in 2001) I continued to work in my Type A job along with my type A personality. After three years I found that I could no longer continue in that role and thus retired. I went about changing my focus on life and now I volunteer in various organizations and stay in contact with others I’ve met also living with MS. Every day has become a learning opportunity. So instead of “Speed Bumping” (quote by Teri Garr) my way through life, I’m learning to LIVE.

God bless you and your family. Your delightful smile is what makes even bad weather feel okay.

Many blessings,
Kris, TN

Janice,

Come back to Houston in April and join us for the MS 150 Bike Ride benefitting MS – we raised $10 million last year – it’s a great event!!

You are a treasure.

Janice:
Your article on MS and the fact that you have it, makes you just more wonderful than you can imagine. I love seeing you do the weather on Fox. I have always admired you and your
“human” antics on the show. I am sad you are having to deal with this disease, but know God can
lead you in all sorts of ways to come to grips with it yourself and to participate in research and public awareness. I did not know Neil also had this disease. I know he is like a rock to you for support and
help. We are fox fans from the word go, so we hope to continue seeing you both!!

Please know we are praying for you and others who have this disease for peace and understanding to work though the rough spots in your day to day life. Some days I know it must be so hard, but
keep your chin up. You have people cheering for you.

Just wanted to let you know that we like seeing you on tv and enjoy your personality shinning
through! Keep up the great work.

We love you… Diane and family …way down here in Waco, Texas!!!!

God bless you, Janice! I was diagnosed in 1992 when I was 20 years into a career with the Navy Nurse Corps. Looking back, I had strange symptoms years before which were attributed to a disc problem, too tight jeans (I never wore tight jeans) or just, “We don’t know. Let’s wait and see.” Of course the symptoms disappeared, so I was crazy, I guessed. The diagnosis was extremely stressful, but as you did, I went after all the information I could find. I had to tell my superior officers of course, and I didn’t know how they would react. I found them all to be supremely supportive. With the help of medication that was available as of 1994 and the continuing support of all of my colleagues, I was able to finish a 30-year career. My advice for anyone faced with this craziness is never take “no” for an answer. Be aggressive in pursuing what you want and need. In 1993 I heard that the FDA’s Advisory Board had recommended approval of Betaseron and I called the Director’s office. When the medication was available in 1994, there was a lottery and I was told I’d get it in about 4 years since my number was somewhere around 45,000. The Navy was allotted doses for 100 people, so I called the Undersecretary of Defense for Health Affairs and was told they hadn’t come up with a distribution plan. I finally found that Univ. of San Francisco Medical Center had some doses and that’s where I got it. I have aggressively pursued research studies as well and am in one now for an oral medication that has helped me a good bit with my mobility. When I was diagnosed, I was dating my now husband, and telling him was another chore. He stuck with me and still stands by me through everything. I know you must be a strong woman. You can cope!
Hang in there!!! Dot

YOU and I were pretty much diagnosed at the same time. I have been on copaxone for two years this past Feb. and I was diagnosed around November of 2005. I really had no idea. I did have a few wierd but mild and occasional symptoms, but then I figured it was part of aging-I was 57 at the time. The real clincher was the dx of transverse myelitis causing some sensory numbness of my feet and then most of my body. Even the it was very mild and I waited for a month to see my internist who recommended the spinal mri where the TM was dx. After that I went to see a neurologist who ordered the bain MRI especially because I have a daughter with MS who was dx’d three years previous at age 20. No one else in the family we know of has MS, but we both grew up in Rochester, one of those high ms cities.

I have always been pretty open about my situation and I am glad you have decided to speak up. I think if a national survey is ever started, and hints of it were mentioned on an MS site I belong to, the I think the numbers will be higher than 400,000 and being more vocal will hopefully encourage more research for a cure or at the least new medications.

So far I am doing okay. The numbness in my feet never went away, but I deal with it. I am a (cantorial) singer and I continue to do what I like to do the most. I wish you all the best. If you ever come to Rochester, I’ love to meet you! sincerely, Ellen

Dear Janice,

I wanted to know something personal about the ladies on Fox News. Since you are my very favorite one, I Googled your name and was shocked to read about your MS.
One thing I know is that your positive attitude will take you a long way. Just keep being the same sweet woman that I have known and remember that you will be in my prayers.
I think Cavuto was right when he said that you will get through this. (he is another favorite of mine)

Julian

Janice,

Just wanted to send you prayers from Sunny Florida.

Also, I wanted to see if you were up for dinner Friday night? Yeah, yeah…I know, I live in Florida. If you wanted to go out, however, I’d be in New York!

Janice,

Getting diagnosed is overwhelming at first; you’ve done exactly the right thing in getting started with a treatment right away. Yep, the daily shots are a pain in the butt…and the thigh…and the arm…but it’s (I’m assuming Copaxone) a good medicine and starting on it early makes a big difference. Stay informed, but don’t obsess. Keep your ears open for new research, but I really recommend NOT spending a lot of time on MS message boards or in support groups, because those tend to focus on the worst aspects of the disease, and disability is not necessarily your future (or mine). Just live your life as Janice Dean, not as an MS patient.

Hi Janice,
I wanted to send my heartfelt sympathy to you the minute I heard of your diagnosis with MS. My wife, Heather, told me the news during ms awareness week. Sorry it took me so long to do this. I was shocked to hear that two of my favorite personalities on Fox have the disease. Heather, who is the regional development manager for the MS society had the opportunity to hear Neil cavuto speak about his experiences with ms while at a convention in Florida. You are both an inspiration and I admire your “can do” attitude. One of the ways I help increase awareness about the disease is by participating with the ms bike tour here in Montana. This will be my third year riding and fifth year volunteering. I am starting to do fundraising and wanted to know if you or some of your friends would like to help me in this endeavor. If so, you can go to my personal web page at http://www.nationalmssociety.org/goto/davidohs. Any help would be appreciated. I am confident a cure will soon be reached. God bless you Janice and Neil.
p.s. If you would like to do the weather from Montana in September we would love to have you with us at the tour. Thank you, David