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Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
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#1 | ||
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Junior Member
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hi there!
Has anyone else had to get a BPAP or CPAP machine since having MG? My breathing at night is terrible. I had a sleep study and that confirmed it. ![]() |
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#2 | |||
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Member
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"Thanks for this!" says: | StephC (12-20-2012) |
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#3 | ||
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Member
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I also did sleep study and am waiting for call now to get machine. My neuro says very common with MG and using machine should provide significant help with general well being.
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#4 | ||
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Junior Member
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Thanks so much for your input here. This is a great site! Glad to know that as far as MG'ers go this is normal. All the best for this holiday season to you all!
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#5 | |||
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Member
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I can't sleep without my cpap. I take it with me even if I'm going to be away from home for 1 night. I have tried to sleep without it and just can't do it. I wake myself up because I can't breathe. I've been using it for about 12 years and am on my second machine. It takes a little time to get used to wearing it at night, but keep on trying and you will find the mask that works best for you. Good luck!
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"Thanks for this!" says: | StephC (12-20-2012) |
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#6 | ||
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Junior Member
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thanks again for all of the encouragement!
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#7 | ||
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New Member
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Quote:
Cherokee23 |
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#8 | ||
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New Member
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I have just been put on a BiPap machine, kind of tough getting used to it.....but I have severe sleep apnea & some COPD.....
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