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Originally Posted by oobadooba
Hi Just was diagnosed with MG and was looking for resources or people in general to share knowledge with as well as someone with simuliar symptoms. This is new to me never heard of MG. I was also told by my doctor recently that I have symptoms in my body.
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Dear oobadooba,
Im so glad you came here! My dad was diagnosed with myasthenia gravis a few weeks after my mom announced my impending arrival. MG has been part of my entire life. On of the most important aspects of treatment plan is your support system. NeuroTalk can be part of that: Myasthenia Gravis Forum:
http://neurotalk.psychcentral.com/forum77.html
This link takes you out of NT to an excellent article Ocular Myasthenia:
http://myasthenia.puhs.org/drspector_ocularmg.html
I hope you'll come back, ask questions, let us know what we can do. Take good care.