My latest little update. After almost 1/2 year, 5 months of fighting the ignorant Doctors and insurance company, I got the letter and now received the C-Pap for my condition called Sleep Apnea. It is most likely a symptom of the Lyme disease or co-infections, but it's something to treat and so I'm hopeful. I received the machine and mask set to level 6 (4-20 levels I believe) to keep air flowing in and out at night. If it helps a restful sleep, there is a chance I will heal faster because I'll be more rested. MAYBE even less fatigue!! I can't wait, and I am also worried that it will not help and will hurt really bad...
The only person I can think of with the same thing that would understand the awkwardness is my grandmother in GA. who suffers 'Fibromayalgia', sleep apnea, and other aches-- And she said it was just a get-used to process.
So that's what's up, so far!
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Quick Update: Disulfiram
5 years ago
this is Cortney Wright again. i noticed you didn't have any comments and wanted to tell you that i'm on like 30 pills a day as well, and you're lucky to have the oxygen treatment for the sleep. i take naps about the same time everyday, that's how i blow off my fatigue and i feel for you on the oxygen.
ReplyDeleteI am a neuro Lyme/Babesia sufferer, and I just started the CPAP machine for sleep apnea(I also take about 30 pills per day. Is it possible that the oxyegen from the CPAP is making my Lyme worse(I've heard that oxygen kills Lyme..
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