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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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#7 | ||
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Hi Alice…..
Talking about roller coasters…… Funnily enough in my experience it wasn´t until my symptoms had become such a ´roller coaster´ that I came to realize that something was wrong with my body and not my mind!! The 4 years of more stable and slowly progressive muscle weakness led my doctor into believing I was obviously on a psychosomatic downhill slide. I followed suit in this belief! And was then left to my own devices for far too long. Ironically, it wasn´t until the myasthenic weakness had changed into a more manic seismic pattern that I realized it actually had nothing to do with a psychiatric illness!!!! The more I experienced the fluctuations the more I realized that glimpses of my original muscle strength were visible and accessible, and that is what inspired me to fight and to be heard. So in a way that ´roller coaster´ was my saving grace. ![]() Annie - on top of a fulltime business - it´s like running your own business to get the diagnosis first! On a more practical note: Medication has helped, finding your place in the´myasthenic context ´on this forum has helped, and now a plan of action at my first real neuro appointment will also help. On another practical note about life, ![]() Last edited by Anacrusis; 09-26-2012 at 01:49 PM. |
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