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Multiple Sclerosis Board Index
Pages: 1 2 3 4 5 6 7 8 Showing 41 - 60 of 151 for chills and ms. (0.010 seconds)


... He Kelli, I'm having the opposite problem, I fell like my face is on fire....all the time. Is it the steroids or the ms???? That is the 64 million $ ? When you're taking tons of meds and have ms and are going thru menopause or pre-men. who knows? I bet even the docs prob don't. I'm sorry. I would check, cause I haven't heard of running a fever for no apparant reason... (3 replies)
... h. I have been on anti anxiety medication as he believe most of my symptoms are anxiety related but I have some real symptoms. The medication helped calm me down and sleep better but I still have physical symptoms. I have been on the meds for almost 3 weeks. ... (33 replies)
... s done yet except bloodwork which I am still waiting for results on. All my tests are scheduled for this week. I am seeing a neurologist but I am not sure it's a MS specialist. The neuro is part if the same practice as my PCP. ... (5 replies)

... MS is unique to each MSer. You might share one or two symptoms with another or none at all. My numbness and tingling did not appear until the year of my diagnosis. Foot drop was, rather remains, constant since 1977. ... (12 replies)
... open and honest opinion as to whether or not you think it could be MS that I am experiencing? ... (11 replies)
... Yes to your question regarding the chills! To be honest the first two and a half months were the worse for me. The nurse said that I would experience flu like symptoms and I definately did. ... (7 replies)
... hi there sorry to hear about your headaches. I to take Rebif for my ms and i had the same side effects. Do you ever get the chills real bad in the middle of the night? ... (7 replies)
... do not stop trying to find out what is causing these issues. I pasted your list of symptoms here and the list of Lyme symptoms under it. You can see the simularities. Lyme can often look very much like MS. It is what my doctors thought I had for about a year. ... (6 replies)
... I'm Sue and I was dx. with "probable" MS in '93. Said they couldn't say for sure til I had another flare. My 3rd child was only 6 mo. old, married, and working full time. It started with double vision. Talk about devastated. I had another flare with my left leg and balance about 6 mo. later. ... (10 replies)
... I dont take anything else besides Rebif. The occasional Xanax when life gets overwhelming and I cant sleep, but I manage my disease mainly with exercise and "mind over matter". Easier said than done. ... (15 replies)
... Hi Jules. I was 38 when I was dx. I was also put on Copaxone, and I also took two ambulance rides to the hospital with it...scary, right? ... (5 replies)
... no matter what happens. I feel EXACTLY the same way! And I thank God that after a year of neurological issues, I finally know what I have. My many docs thought I had MS or it was just in my head. ... (16 replies)
... able...however, the flu like symtoms are KILLING ME. I now spend 3 days a week with the chills, fever, aches, and pains which is totally putting me out of commission. ... (5 replies)
... Advil to start. I thought that was a little over the top, but, in the beginning while your body adjusts to the med, it turned out to be good advice. In a year and a half, I had one reaction. ... (10 replies)
... I see these threads on here all the time and I know I posted a similar one before. ... (9 replies)
... I am sorry to hear of your troubles. My docs thought I had MS for about 9 months but there were some things that did not add up and my MRIs were clean. finally, thankfully, Someone pointed me to Lyme. I was diagnosed last month. ... (1 replies)
... Maggie, I was unable to take Copaxone because of "end of life experiences" and, finally, a grand mal seizure. Avonex made me feel flulike (general aches, fever, chills, etc.) that was getting worse, instead of better. I am now taking Tysabri which is an IV infusion once every 28 days. It is so nice not to have 4-5 days of the flu each week. However, before starting on... (15 replies)
New avonex ????
Jul 15, 2007
... amily. I hear they have new pre filled injections. When i was using them i had to mix everything up myself. Just wondering if its really easier, i'll be seeing a MS Nurse on friday for her to show me how tho do them all over again. I dreaded the after effect of chills and fever, do the new Avonex have lesser side effects. ... (6 replies)
... Thanks for your useful info.I take 1 Alleve but will definately consider 2 if the side effects persist.I'm glad you mentioned that Rebif is not a cure cause I sometimes forget.I guess that the dizzy spells have just about gone away since I started the shots.Please keep me posted on your results. (10 replies)
... I still take two Advil with my injections. Tried without and had a bad case of the chills. ... (10 replies)




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