Hi y'all.. I just saw my Neuro yesterday...not so fantastic news. It seems my disease is fairly active, and he noted deterioration in my left leg (Babitte's...
I was diagnosed with remitting-relapsing MS in 1980 . For a number of years I kept working at various jobs but having frequent attacks I decided to quit and...
Hi y'all There seems to be problems posting the replies to messages on our board...the threads...I am not sure if it is Yahoo or the current set up... I will...
OK... WE can reply-post once again. If you do not wish to receive any posts directly to your email, simply edit your membership and click on the button that...
Hi I'm new to this site. I've been just recently told that my family Dr. beleives I may have MS, since last fall I have tremours all on the right hand side of...
Hi!, I' m not new to this but, I've been there, it started with my whole left side. I had a lot of knumbness, twiches in my face & my hands....now I'm on good...
Thanks for the reply, At this point I'm on meds for the tremours, pain & inflamatories. But I react to meds very badly!! So far this 3 meds. are working for...
Your very welcome!, I know I did the spinal tapp!...not fun? My fluids came back clear?, the M.R.I was, my problem, My dr. said it looked like it snowed on my...
Well my story is a long one, but here it goes. My first son was born 17 years ago, I became nausaus and headacheas and a stiff neck. same happended after my...
hi I totally get it!...everything your discribing is so familiar to me! I think it's great you have 3 kids, that's the 1 thing I did not have, although...it's...
I'm not sure where you live, but I found out the hard way on how to get an MRI sooner than the awful 6 month wait. It could be different than where you are,...
Hi!, I live in Las Vegas, NV...USA, I write back & forth with a couple of girls from Can. They are dealing with MS too! I agree the MRI IS THE BEST, WORST...
Thanks for the input:) I live in Ontario, Canada actually. First thing next week I will call, the hospital and ask about making my appointment sooner( which...
Your very welcome, OK? 4 & 4.....STRESS IS AN UNDERSTATEMENT!! I helped raise 4 kids right before I was diagnosed! I found I needed to take quite time for just...
I didn't know that MS could give you headaches & make your face tingle. I've had problems with my left Jaw since I was 16 yrs. old. & my face does go tingle &...
I wonder if my headaches are a symptom , or a way of me dealing with stress, I have always had them:) Yesterday was a good day, I think I let go of some of...
Wow Michel, I really don't know about the headaches....I know stress & headaches go Hand & hand!!!!!!, As far as sympathy....I love my Dr.'s because they have...
Well, Jen, Anything is possible, no cure? no real answers!...I do know when I first had face issues, I was told it could be "Bells Palsey", THAN I started to...
Michelle - I could not agree with you more on the system lacking sympathy. When I was told to sit and wait 3 months to get a diagnosis and just stay at home...
I may be new at to this but the way I see it YOU have been living this way for a while(am I right!!) Just because the Dr. may finally know what your body has...
I can relate with that Kim, when they told me in 95 that I had Lymes desease I was glad. at least I had something to work with and I wasn't going insane:) Now...
