This Is MS Multiple Sclerosis Knowledge & Support Community

Posted: **Wed Oct 17, 2007 4:59 am**

LAnBfflo wrote:Hello everyone.
I'm really happy I came across this site. It's been almost 3 years (2 weeks shy) since I was diagnosed.
I've been on steroids, beta seron, tysabri, and ivig with steroids. My initial diagnosis was RRMS, but found out Monday my new doc thinks it's SPMS. I'm so-o-o-o-o thrilled, as you can imagine.
I can't believe I haven't found this sooner!
Anyway, I'm really happy to have found this site.
See y'all around.
-LA

We're glad you found the site, but sorry that you find reason to be here!

Not that my saying it is conclusive evidence, but I think you'll find in the near future that the situation for SPMS and PPMS isn't as dire as you'll be led to believe.

Bob

Posted: **Wed Oct 17, 2007 5:19 am**

Hello LA,
Welcome to the site. I wish I could remember how I first stumbled across it, but I think it should be compulsory for neurologists to hand out the address with every diagnosis they give!

Posted: **Wed Oct 17, 2007 11:29 am**

Hi Dom, despite the fact that thisisms didn't even warrant mention in that MS internet information study, we're right up there with the BIG players on the Tovaxin "links" page http://www.tovaxin.com/links.htm
Bob