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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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Grand Magnate
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I saw your post in the "Your diagnosis, treatment and other information" sticky. That is where people put info about their "MG journey" for others to read. So I thought I would start this post here with the info you put up there.
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If you have polymyositis, they should be checking your blood for CPK, creatinine phosphokinase. That disease is often checked out by a rheumatologist, since it is an inflammatory ("itis") disease. If you have a primary doctor, they can check for basic things like thyroid, complete blood count, B12 or other vitamin levels, etc. One thing that might help you, since you sound overwhelmed, is to write down every single symptom you are having, when they occur (i.e., always or only in the morning) and what is the severity of each one. You might start to see a pattern and be able to relay them to your doctor(s) better. You need the help of doctors. There's only so much we can do here. I hope you can find someone to help. Annie Last edited by AnnieB3; 01-08-2011 at 03:31 PM. |
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