This Is MS Multiple Sclerosis Community: Knowledge & Support

**Posted:** Wed Mar 30, 2005 7:15 pm

Hi,

I'm new to thisisms
I actually came on to find out info on lobbying for aimspro in Canada and if anyone had actually done anything here yet. I know it's still a long process for licensing in the UK but I'd like to start raising awareness here as well.

Great site!
Lace

**Posted:** Wed Mar 30, 2005 6:19 pm

Just introducing myself. Names Jen, 29, and I live in Hot muggy FL.

Thanks for having me.

**Posted:** Tue Mar 29, 2005 6:19 am

Hi,
I'm new in this group.I have got MS 12 years ago.I'ma 36 years old.I'm on Rebif years ago.Noone could possible that I'am MSer.I have put 2 dental implants last year.I havn't any problem with it and havn't notice that have problem with my MS.I'm going to have MRI at the end of April.That is my first exam since I have put dental implants.What do you think about all of that?

**Posted:** Wed Mar 23, 2005 11:22 am

Yes, it's sunny!!!

Great site BTW

:wink:

**Posted:** Tue Mar 22, 2005 7:55 pm

Hello to all... I just came upon this web site by pure accident. After years of looking, it's wonderful to find an MS site that is not backed by a drug company in some way or another. Bear with me if I screw things up, as I learn what I'm doing here. It took me forever to figure out how to post this! This site has a good feeling .. I'm glad I found you. ...

**Posted:** Tue Mar 22, 2005 5:36 am

Hello,
Just stumbled on your site while checking info on Aimspro and it looks like a good place to hang out.

I was dx'd in '02. On SSDI in Oct '04 and not missing work at all.

I do much better without the stress of my job and have learned my limits and adhere to them most days. LOL

I have been married 39 years, have 2 adult sons, a DIL, and a beautiful granddaughter, ...

**Posted:** Sun Mar 20, 2005 10:12 am

New to the site. My wife was dxd rrms in May 2002 at age 43. The Neuro put her on Rebif, she never really tolerated the drug, persistent flue like symptons and she had a minor relapse in Dec 04. Had a Tysabri infusion last month, but as you all know that's gone now. We'll see the Neuro next week, we're thinking he'll put her on Copaxone, he has acknowledged that the Rebif has been ...

**Posted:** Thu Mar 17, 2005 7:28 pm

I've had for 12 years. I'm 43 and live near Chicago.

**Posted:** Mon Mar 14, 2005 2:39 pm

I guess this is for introductions.

I am 39 year old single male now living in the Scottish Borders about 1 hour South of Edinburgh.

I was dx with ppms in 2001 while overseas and have now returned to Scotland to settle down a bit. I was working until one year ago, but the MS put that to a stop.

My legs, balance and sight are the main areas I am affected. I use a ...

**Posted:** Mon Mar 14, 2005 9:30 am

Rats, I was holding out so much hope for the goats serum but they have stopped the trial now.
Lets hope something will help with my walking soon
julesx :)

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