On Fri, Oct 16, 2009 at 8:24 AM, Grace M. <grace...@gmail.com> wrote:
> *Hi Deb, * > ** > *Re: Tysabri. I go to a very large teaching and research facility for my > Rituximab infusions, and have a lot of MS friends that are using Tysabri. > Many have had really good results, including a reduction of relapses and > improvement in their EDSS, and stable lesion loads. Most seem to be very > happy with it.* > ** > *Gracie * > > On Fri, Oct 16, 2009 at 7:04 AM, Deb Monteleone > <aiki...@optonline.net>wrote: > >> Hi, I am thinking of going on tysabri, anyone out there on it. If so do >> you have side affects and do do feel better? I'm currently on copaxone for >> just over a year. Starting to forget my shots and spoke to some people >> who's symptoms got better on tysabri. >> >> Thanks for any input, >> Deb, Long Island >> ny >> > >
