Thursday, February 16, 2012

All SharePosts Relating To "Copaxone"

Expert_badge Amy Gurowitz

Amy Gurowitz

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Writer, Educational Designer, Non-Profit Founder, Dx in 1988
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MSOL Radio: Show 9 An Alternative Approach

Tomorrow! Wednesday, June 8th-8pm EST, MSLOL Radio will speak to three guests who have a story to share about their alternative approaches in dealing with MS. (where to go? info below)   Rachelle Breslow was diagnosed with MS in 1968 and didn't accept the neurologist's responses to her questions about living with the disease. Told that... Read moreChevron
posted 06/07/2011, comments (0)|
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williamd

williamd

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recently diagnosed with RRMS in December 2010
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Rebif or Copaxone?

After watching videos, reading books and websites, I'm still having a difficult time deciding which treatment to follow. It would be great to hear from someone who has tried both Rebif and Copaxone and can compare the two in terms of side effects (I know everyone is different) and effectiveness.
posted 01/07/2011, comments (2)|
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AGSerra1

AGSerra1

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Has been a while since I last wrote on this site .....
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New for me

  Hello out there .. been a long time since posting .. saw many reposes to a questions referencing Marinol & Sativex .. thanks to all who did reply !   Having my MS now 9 years and experiencing new issues it was finally nice to hook up with a Neurologist that was able to expand on my MS .. back in July of 2006 , I had written about... Read moreChevron
posted 12/02/2010, comments (2)|
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David Madison

David Madison

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I was a factory laborer before MS; now I write astronomy articles
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New MS Drug Ampyra

Vicki, it has been a while since I talked here.  Don't know why I stopped.   I have tried both Rebif and Copaxone for my PPMS, each for about two years.  As you probably know, they are not supposed to cure MS, but rather slow the progression.  It is therefore hard to know whether they are working.  How do you judge how... Read moreChevron
posted 11/28/2010, comments (7)|
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KristinaYellow

KristinaYellow

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Living With It
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Betaseron v. Copaxone

I've been on Copaxone since early this year when I was finally diagnosed. Now I've been having some serious fatigue problems, dizziness/fainting, and terrible reactions to the shot (the flush/nausea/hard to breath stuff) plus some painful shots. So my doc wants me to try Betaseron thinking it'll be easier. Here's the catch--I'm a stay at home mom... Read moreChevron
posted 09/17/2010, comments (8)|
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