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Hi all

Posted: Fri Nov 13, 2009 5:16 pm
by Habenoughyet
I guess, as the rest of you, I'd rather not become a member of this type of group... But, I am.

I'm a 40 yr old (... tomorrow 41 :lol: ), male. I live in Montreal, Canada. I was diagnosed 6 months ago with MS after the MRI scan. My neuro (who is an old quack) says its cyclical, but I've never had an "attack", or remission for that matter, that's why I believe it's primary-progressive. I've been reading up on this horrific disease, and I've finally had the courage to discuss with others that are plagued with it like I am, and that just want to share some of their wisdom or thoughts on living with MS... God knows, there must be millions of lessons to learn. I simply want to get to know you all, to share our common problems and encourage us into knowing we are not alone in living with this...

I'm also an avid hockey fan (Go Habs Go!!! :wink: ), and played guitar (Stevie Ray Vaughn-Hendrix blues).

HEY
(Hab-Enough-Yet)

Posted: Fri Nov 13, 2009 6:02 pm
by LoveActually
Welcome to TIMS and Happy Birthday!!!

Love your quote. :lol:

Posted: Fri Nov 13, 2009 6:10 pm
by Habenoughyet
LoveActually wrote:Welcome to TIMS and Happy Birthday!!!

Love your quote. :lol:
Cheers, Love... (he said with a "James Bond" accent) :wink:

HEY

Posted: Fri Nov 13, 2009 8:34 pm
by skysoldier
Welcome ,

Happy Birthday.

We all try to understand ms, it's a quest.

ms takes the old self and gives us a new normal.

That new normal is all you need to contend with.

I've been dx for six years , for me a lot has changed.

all you can do is be flexable, bend a lot but don't break.

ms sucks,

Sky

We must be twins,

We have the same birhtday, to this site.

Posted: Fri Nov 13, 2009 9:01 pm
by Habenoughyet
skysoldier wrote:Welcome ,
We must be twins,

We have the same birhtday, to this site.
Cheers... I guess we do.

Keep the faith!! :)

HEY

Posted: Thu Nov 19, 2009 6:21 pm
by DM
Hey Habs fan,

I live in Ottawa, not a Sens fan, and grew up in Montreal. I was diagnosed in July 2006, and have no issues with the disease. I am nearing the end of my 2 year study with teriflunomide, and been good all along.

Anyhow, we are all here to offer any advice and provide whatever support is needed.