This Is MS Multiple Sclerosis Knowledge & Support Community

I'm not really sure how they truly come up with an efficacy rate for any drug, when it is true that lesions and symptoms can come and go on their own.

Thanks Harry. This really helps.

Does anyone know the efficacy rate of Tysabri? I tried to find it on pubmed, but I don't really know where to look in the endless reports.

I was diagnosed 7 years ago. I remember the feelings you are going through. I remember coworkers and friends all trying to carry stuff for me when carrying stuff was not where my problems were. They knew very little about MS and that was one way they tried, but it just made me feel weak and angry. I...

Thanks Lyndacarol. I appreciate your words.

It took some restraint.

Yes, I have asked and made suggestions right away and over the years. I don't think it's expecting too much, but maybe I shouldn't have shared it here. Thanks for the link though.

I haven't had a neurologist in a while so my gp recommended one to me. My gp knew I was into the more natural approach and definitely approved with it, so I trusted her recommendation. My new neurologist walked in the room and the first thing I noticed was her obviously botoxed face, in addition to ...

Thank you lyndacarol. I look forward to being part of things here.

I know it can be scary when you are first diagnosed. It is smart that you came here for support. I agree with NHE with staying active. Walking, yoga, swimming are all really MS friendly. Many people with MS can do much more. Also, do your research before you take any medications. Try to eat a health...

Hi. I am new to this site, but have been diagnosed with MS for about 7 years. I do ok. I have some cognitive issues, neuropathy in my right leg, pain, heat and fatigue issues, bouts with double vision and a few random odds and ends. After all this time I still don't feel supported by my friends and ...