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Re: big thanks!

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Isela,

Sounds like you have gotten very good advice so far. Just wanted to

share that I've been on Avonex since I was diagnosed October 2002. I

am still suffering from the side effects the day after the shot.

Today has been horrible for me. I will be discussing this with my dr.

on my next visit.

~mo~

> whew! sooo glad to hear the responses. it seems like copaxone is

> the way to go, and I'm pretty sure that's the way the doctor is

> leaning. I'm a lot more comfortable going on that than the

> interferons, due to side effects, so very good news. again, thank

> you everyone, I really appreciate all the replies. you all have

> already set my mind at ease alot.

> Isela

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Hi the needles come with Copaxone also. If you Copaxone is what you want to take you can visit there web page. You don't need to be a patient to register with them to get full access.

http://www.copaxone.com/index.asp

I like there service because through MS Watch you can keep in contact with a nurse if you have questions.

You can also talk with others that use Copaxone.

Bill

big thanks!

whew! sooo glad to hear the responses. it seems like copaxone is the way to go, and I'm pretty sure that's the way the doctor is leaning. I'm a lot more comfortable going on that than the interferons, due to side effects, so very good news. again, thank you everyone, I really appreciate all the replies. you all have already set my mind at ease alot.Isela

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