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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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09-16-2013, 09:05 PM | #21 | ||
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09-19-2013, 12:00 AM | #22 | ||
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I posted earlier about the tactics I use to survive in the heat.
Unfortunately, recently, the weather here in California has been unusually hot AND humid. Our summer started out unusually mild...... Hot = I have been able to deal with (mostly). (See previous post). Hot AND Humid = has been sinking me and my MG....... This atypical weather for Southern California (near the beach) finally has me believing that this "Global Change" is real, folks!! (Whoops, sorry, I guess this statement is for another forum). Back to the topic: Surviving by staying inside in air conditioning and hydrating (drinking fluids) often. And by "doin' nuttin' honey.........." |
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"Thanks for this!" says: | cait24 (09-19-2013) |
09-22-2013, 05:15 PM | #23 | ||
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I too feel the effects more when it is hot. Sometimes it will make the symptoms worse. Then it will take several hours up too a day too get back to where I was before. I thought it was just me being from up North but living in MS.
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"Thanks for this!" says: | cait24 (09-22-2013) |
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