This Is MS Multiple Sclerosis Knowledge & Support Community

I am going to pay close attention to the web-cast tomorrow at 12:00 pm, I am deep in SPMS with my fingers crossed(with tape,:lol: ).

Thanks sams, I'm all set to go . Dr. Murray was my Neuro.

welcome musicman, It seems there is alot of MS in Canada....


I to am very interested in CCVSI.

ToddH

Hi sams, I'm in Truro (not far away). I was dx'ed in 2001 with progressive MS. I travel to Hfx. for my neuro appointments. Do you also? It is very hard when you first learn of the disease, and I'm not sugar coating it is much harder some days than others. Just remember to keep fighting, do not give ...

A person from Nova Scotia, we had a sailboat named the Bluenose. It was fast in it day.

Hi globab, yes my hfx visits to my neuro Dr. Bahn I hate so much. It reminds me of how sick I am.

jimmylegs, I checked out that link and read some great news! I know it is different for everyone, but I think this may be worth checking into deeper.

lubylu, do you still live in NS? I am in Truro.

scorpion, I promise not to be too vocal in my rants. hehe

thanks all

Hello all,
I'm a semi-retired husband with SPMS. I was Dx'ed in '01 after a looong and tiring battle. I have all the usual symptoms, fatigue, spasticity, bladder, etc. I am putting a lot of faith in this newer CCVSI, am I being too optimistic?

ToddH