This Is MS Multiple Sclerosis Knowledge & Support Community

Hello, It's been awhile since my last post. After a great deal of thought, I decided to give Tysabri a try. My Nuero was opposed as my symptoms have not (in his mind) dramatically changed since my dx 4.5 years ago. First, I was on Avonex fo about a year, then swithced to Rebiff. My chief symptoms ar...

Friends, I met with my doctor on Tuesday here in San Francisco, CA. The MS docs and the infusion center are getting trained and certified within the next couple of weeks. So, my doc infusions will commence in mid August. I suspect it will be the end of August. Anyway, that's what they're telling us ...

Each of the FDA committee members are intelligent, qualified people. The discloure was appropriate and required. In my experience, it is indeed difficult to find a committee that is 100% comprised of people without some percieved conflict of interest. It's the disclosure that's important.

Dear Friends, Interesting post and request to ban Harry Z. I find his comments to be "anti-Tysabri." Of course, Harry Z would understand his post as merely putting forth a different perspective. It's difficult to understand a person's motivations, especially in this type of forum, so who r...

Friends, I enjoy this website, it is informative, interesting, and represents a wide variety of opinions. I hate this disease and remain frustrated that there are few treatment options available for us. As patients, we must be informed. That being said, I do not care if Tysabri generates profits for...

Friends, A new member to the this great site. I am a 34 year old male living in San Francisco, CA, dx three years ago with rr ms. My doctor says I am stable with Rebif, notwithstanding the constant mild numbness and tingling in the legs, arms, and face. I am interested in taking supplements as well,...