I have had MS for about 11 years. I am currently taking Copaxone 40 mg (about 2 years). Previously took Coapxone 20. I did try Tecfidera, but could not deal with the hot flashes. I was working at the time as a full time nurse, my patients would say "you ok, you look like your having a heart attack". I've had a recent relapse that started in October. I have vision issues and depth perception issues. I had to leave my job because I could not assure my patients safety with me at the helm. I just went o my neuro, he suggested that I try Aubagio. I seem to be sensitive to medications. I read many of the Aubagio posts and will continue to check back for new information. I have about 1 month before I will start it.
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Diagnosed 2006, RRMS. -
Sorry you've been on a med-merry-go-round. Can't be fun.
I've been on Aubagio 1 1/4 yrs, sx have been next to nothing.
I wish you the best."Hope for the best and plan for the worst. That way, all your surprises will be pleasant."
Verin Mathwin, The Wheel of Time by Robert Jordan -
I started Aubagio 2/22/16. After a few years on an injectable medicine.
I am INLOVE with the pill. No more needles.
I am probably jinxing myself, but I have had absolutely no side effects. I wish I switched to an oral medicine earlier. But oh well.
Good luck!Comment
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Thank You
Thank you for your thoughts. I do feel better about the switch.Diagnosed 2006, RRMS.Comment
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