My RRMS suffering partner has had a noticeable degradation in eyesight this year (she started on Copaxone in Feb 2010).
She is now exhibiting many of the symptoms of Myasthenia Gravis, but that seems to be very unusual to have this along with MS.
Can the two in any way be connected?
Any thoughts on this or what may casue the sudden problems with eyesight (side effects of Copaxone etc?)
MS and Myasthenia Gravis
- lyndacarol
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MS and MG (myasthenia gravis) are both in the autoimmune disease category. It is not uncommon for a person diagnosed with one autoimmune disease to be diagnosed with a second, or even a third.
In fact, the December 2010 issue of InFocus, the quarterly publication of the American Autoimmune Diseases Association (www.aaarda.org) has a front page item from Carol Berger, of Horsham, Pennsylvania, who says, "… I myself have been diagnosed with lupus, rheumatoid arthritis, ankylosing spondylitis, fibromyalgia and Ménière's disease. I also have asthma-related conditions.… I am one of the 50 million Americans who live with autoimmune diseases, not just one disease, but several."
In fact, the December 2010 issue of InFocus, the quarterly publication of the American Autoimmune Diseases Association (www.aaarda.org) has a front page item from Carol Berger, of Horsham, Pennsylvania, who says, "… I myself have been diagnosed with lupus, rheumatoid arthritis, ankylosing spondylitis, fibromyalgia and Ménière's disease. I also have asthma-related conditions.… I am one of the 50 million Americans who live with autoimmune diseases, not just one disease, but several."
the klenner protocol (old but good for its day) addresses both ms and myasthenia gravis. you might want to check it out. search google for the term 'klenner4' and it will take you to a relevant article in townsend letter.
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glad to help. don't take the crude liver thing too seriously. i mean you can if you want, but i didn't and it still did wonders for me (i did a really half-@$$ed oral version but it was still awesome).
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