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Treating MS

Treatment *

Well I have been diagnoste with MS after 4 MRI's and a spinal tap. the doctor has sent me the names of 4 different drugs and has asked that I research them before we sit down and determine the best procedure to follow for my situation. Tables:  Gilenya,  Tecfidera Infusions:  Ocrevus,  Tysabri Any experience… Read More

Copaxone *

Hello-  I don’t know if anyone will see this or respond to it, I’m unsure of how this site works.  My name is Amy, I was diagnosed with MS two years ago but am only now able to start treatment related to multiple pregnancies. My doctor has prescribed low dose Copaxone injections 3x/week. He said this was a… Read More


OK. So I do not normally contribute to blogs, discussion, conversations etc. as I fall firmly into the "lurker" category. However, I do check out this site often and have appreciated everyone else's contributions. So why contribute now?  The reason I am typing now is in about 4hrs I am going for my first… Read More

Ocrevus. Would anyone know *

if someone had melanoma cancer, no treatment prescribed just removal of the cancer. Still haven’t been 5 years cancer free, actually still doing CT scans on lungs and  pancreas. Haven’t completed the 4 month test to see if spots grew. Would I be required to have a whole body scan to make sure I’m completely… Read More

New to the area*

I've just moved to Lindon, UT and am needing to get established with a new MS Specialist in the Salt Lake City area. Would appreciate suggestions on who to see. Who is your favorite MS doctor? Thank you!   Read More


I've been taking Copxone since late November so I know it hurts, but last night was b-a-d. The past 2 injections (including last night) were leg days. The first one, I used the autoject for and it was more painful, and bled a bit more than my normal. Then last night, I injected the other leg manually thinking… Read More

For anyone not on medication

Hello all! So I was diagnosed on April 30, 2018 and was put on medication in Mid-June. Since then I have started my now 3rd medication due to being allergic to the first two. I now fell I may be allergic to this one but may not know yet until next week when I do my first full injection. So here it is; I just… Read More

Newly Diagnosed: Ocrevus or Tysabri?*

I was recently diagnosed and because of the amount of lesions in my cervical spine, my doctor is recommending an aggressive treatment. She told me her top two choices are ocrevus and tysabri. I've done a decent amount of research and am leaning towards tysabri. However, I just talked to a friend who has had MS… Read More

Side effect?*

Hi, I got my rituxin infusion on December 27th I noticed a few days after I have a bruise on my inner ankle and it hurts when I push in the bone. It also has been swelling. I went to the doctor and they ruled out things they think it could be. I’m at a lose and am not sure if this is a side effect of rituxin… Read More


I saw my neurologist today.  We have been discussing switching me from Gilenya (which doesn't seem to be doing anything for me) to Ocrevus.  I almost pulled the trigger on the switch today (at least the preiminary parts) but I chickened out.  I am terrified at the idea of stopping Gilenya because some people… Read More


Failed Avonex, caused depression. I started Copaxone in January and was doing fine until my liver enzymes came back way to high. Now doc wants to start Gilyena ..... Thoughts anyone? It seems to have a lot of side effects........ Ready go!!!! Read More

Gilenya & Low Lymphocyte Count*

I was diagnosed with MS this past February. I started taking Gilenya in April. After about 2 months on Gilenya I had labs done and my doctors noticed a drop in my lymphocyte count which is what they were expecting. Fast-forward to about 6 months on Gilenya. I just had labs done again and my lymphocyte count… Read More

Alpha Lipoic Acid *

Hello! My Neurologist recently suggested I try 1200 mg of Alpha Lipoic Acid.  There are so many brands on the market that I do not know what brand to chose that will provide a high quality supplement.  After speaking with the doctor, they recommended that I find one that has been USP verified.  The only brand… Read More

anyone else on Tecfidera ?*

hey everyone ! It’s been a while since I’ve been on here.  since being diagnosed back in April things have been pretty up and down. My doctor had me on copaxone however I needed to be taken off due to an allergic reaction. Now I am on Tecfidera and haven’t had many issues except one of the issues is a rash. Two… Read More


I’ve been hearing a lot recently about stopping medication for MS patients.  I’m only looking for personal opinions and would never do anything without Physician recommendation.  What I’d like to know is if anyone has completely stopped all MS medication, how long it’s been, and how you’re doing?  Also curious… Read More

Ocrevus Side Effects *

Hi, I just received my second treatment of Ocrevus for my MS and so far the treatments which are every six months seem to be working ok. However, after each treatment I get horrible stomach aches and such bad muscle cramps in my calf muscles I can barely walk. Does anyone else experience this or anything… Read More