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| Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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| Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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07-16-2013, 04:23 AM
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To summarise quickly I have had symptoms for 3 years. I have been taking Mestinon for the last 18 months and it has improved my symptoms. All the tests I have had are normal. The neuros believe I don't have MG because my weakness is described as" collapsing or giving way" has anybody had the same experience with neuros please?
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Collapsing muscle weakness.
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