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03-05-2009, 11:30 PM
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I am still trying to learn about MS, but there is so much information that it is quite overwhelming. My new Dr. feels strongly that I have Primary Progressive MS and suggests I try Copaxone. From what I have read, it sounds like Copaxone is more helpful for Relapsing Remitting MS...
I'd love to hear from others with Primary Progressive and what have your experiences been. I live near Minneapolis and am looking for a Dr. that has some personality, because so far I have been seen by two neurologists and have not felt so comfortable with either one.
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Amy DO WHAT makes you happy, Be with WHO makes you smile, Laugh as much as you breathe & LOVE as LONG as you LIVE . July 2006- First significant SXs, suspect it started back in mid 1990's 1/21/09 - Positive MS Dx 2/17/09 - 2nd Positive MS Dx 4/2/09 - MS Dx 3rd Neuro - finally found the Dr. who has the characteristics I was looking for . 10/8/09-optic neuritis flair, Cog Fog, chronic headaches 5/4/09 - 12/15/09 Copaxone 1/15/2010 - First Tysabri Infusion - 3/25/16 - Last Tysabri Infusion 3/3/16 - signed the documents to start the Lemtrada journey 4/25/16. Lemtrada begins. |
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Primary Progressive MS and Copaxone???
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