This Is MS Multiple Sclerosis Knowledge & Support Community

I am so glad to read these posts on Rituxan, and thank you all. I have resisted taking Rituxan, despite my neurologist's enthusiasm. When I inquired how people survive with an immune system so compromised (i.e., B cells down by 90%; and T cells at 55%), he answered, "You don't need B cells. Th...

I was recently approved for this medication. I am also on the much younger spectrum in the population of MS. Does any one have any long term experience with the medication? For example: Can I go into remission? Is this decided on MRIs? How are organ functions long term? Long term side effects if I c...

Hello, DMD is only a small part of progress. As ElliotB says the most important thing is getting healthier. You may start with balancing your minerals and vitamins. Being physically active, maybe going to gym. A balanced diet with low fat intake. If you spend time and care of yourself, you will man...

ElliotB wrote:The 'common' thought on DMDs is that IF you are going to ever go on one, going on sooner rather than later is probably the best course of action.

But IMHO, working on health in every way is equally if not more important. I do both.

Thank you so much! Will definitely take this into consideration

jimmylegs wrote:can i vote if i'm over 2 x 20?

Yes you can

I am in the same boat! Have you made a clear decision and where are you now?... 8 years later

I feel the same way now, glad to know we're not alone.

I am just curious to know what your symptoms were that led you to understand that you have MS, besides the lesions on your MRI. I have those too

Hi everyone :smile: ! I was recently diagnosed with MS about 3 months ago, I was given steroids and I feel better ever since. Me and my family are very hesitant on treatment (Rituxan). I have also received 3 second opinions. Are there any other younger members that have had experience with this. Can...