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I have taken Copaxone for going on eight years total now, with a 3.5 year break in between when I was on Tysabri.
I haven't heard that either. |
I did find this, from 2008. Two of the authors are among the inventors of Copaxone, and the study was sponsored in part by Teva, the company that makes Copaxone, but the study results might still be worth considering. They are talking about experimental autoimmune encephalitis in mice, though it is the closest thing to an animal model for MS that there is.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2516229/ |
See, studies like that make it more aggregating that we don't have a better test for an MS dx. It also does state that it does not repair the myelin, though adults aren't lacking in the ability to repair, repairs to the myelin are still unstable (that darn ionic bonding :( )... But it does so the importance of early detection.
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http://www.ncbi.nlm.nih.gov/pubmed/24934599 |
I haven't heard of this. I'm sure if it was well documented and true, all of us MSers would be on Copaxone. Neuros wouldn't even consider any of the other DMDs.
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Quote:
They can suppose and conjecture all kinds of findings, but the proof would be New myelin sheaths. Havent heard of any???:rolleyes: |
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