This Is MS Multiple Sclerosis Community: Knowledge & Support

Hi to everybody here!

I've read a few threads on this board now and then over the years but never got around to joining.

I already belong to several MS message boards, and I've been on them for 5 or 6 years.

This place looks nice, and I hope to take part in some discussions here.

I was diagnosed with SPMS many years ago. I was on Avonex for 3 years but had to stop because I passed out and fell one night, a few hours after a routine Avonex shot. Now I'm not on anything, but Copaxone could be a possibility.

I look forward to visiting here! Happy 2007 to everyone!

hi agate, HNY! and welcome. ttys!

Hello Agate and welcome to the board. You will like it here, there are some very informed people who post here.

Lew

Hello there. I'm SPMS too- but quite mild. If you're thinking about a new drug regime there's lots of info and personal experiences here to help you decide. All the best.
Muu

Thanks for the welcomes, jimmylegs, Lew and Muu!

It's really nice not to be ignored.

welcome to the group

chris

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waiting for answers

Chris, that's a good choice of a user name--REDHAIRANDTEMPER. Lets people know right away that they should watch their step! (Just joking!)

lol..well i am really sweet to be honest..maybe just a little wicked..but yes the name tends to help out from time to time...lol....where in washington state ya from...i lived in spokane and in bremerton?

chris

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I just found out what an agate is...very pretty....see, I am learning from you already and NO, I am not embarrassed that I did not know
NN

Chris, I'm in Tacoma. "The City of Destiny" is what it calls itself (I'm not sure why).

lived in washington state for most of my life....so was just wondering..lol..

chris

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agate, I poked in on your other thread, but wanted to issue another warm welcome. Thanks for joining us!

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Disclaimer: Any information you find on this site should not be considered medical advice. All decisions should be made with the consent of your doctor, otherwise you are at your own risk.

Hi Agate,

It's nice to see you here! This is a nice forum. I joined it a couple of years ago, then forgot I had joined. I came back and found I was already a member. So I just started really posting a couple of months ago.

I read your bio in the golden years forum, and enjoyed it very much, even though I've read it before on other forums.

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Take care, Ewizabeth Previously Avonex, Rebif & Copaxone RRMS ~Tysabri, 31 infusions, ended 9/09. Starting Copaxone 12/09, waiting for Cladribine to be approved in 2010.

Thanks so much, Arron and ewizabeth.

People are probably thoroughly tired of reading my bio by now! I used to belong to one and only one MS board, and then it became two, then three. Now I'm afraid it's up to 5.

No way, I'm proud to know you with all of your accomplishments, I like reading about them, besides, we both like cats and flowers. Also, I think I belong to... let's see, from 5-7 MS boards. Yikes!

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Take care, Ewizabeth Previously Avonex, Rebif & Copaxone RRMS ~Tysabri, 31 infusions, ended 9/09. Starting Copaxone 12/09, waiting for Cladribine to be approved in 2010.