Mouth Breather for life, due to nose functional issues.
About 18 months ago, I both had a new kid and moved into a new house. Was tired all the time no matter how much I slept. Blamed it on the kid, but as the kid grew I realized it wasn't that. At the same time my allergies were getting worse and worse.
So about 2 months ago went and did all the tests, I did a home sleep study, did a full allergy study.
Allergy study told me I was super allergic to dust mites. Makes sense with the new house timing, this place has like 5000 square feet of 20 year old nasty carpet.
Home sleep study gave me an AHI 15, and I was prescribed CPAP with a pressure of 6-16.
During the 2 months I was waiting for my insurance and the CPAP store to get their crap together, I tore all of the carpet out of my house. Found some real sweet hardwood under, but that is a story for another day. Also adjusted my allergy medicine to get my sniffles under control.
Out of curiosity, I got a little finger mount O2 sensor. The first night I ran it, found something like 10 events where my O2 dropped in the 85-90 range. Did some research about how bad back sleeping is and I made myself sleep on my side. Since doing that, my O2 levels are "fine". Average of 98%, 1 or 2 dips down to 95% and nothing worse.
Now my CPAP machine finally arrived. Using OSCAR to look at my stuff. I was only able to tolerate it for the first 2 hours of sleep last night, but it record 8 CA events, and 0 of anything else. From what I read, this might be CPAP causing CSA in me. I literally wake up feeling like I am drowning, and have to tell my brain BREATH STUPID BREATH, and then I pick up breathing again. I had 0 other events.
is it possible that my fixing my allergies and sleeping on my side fixed my problems? And my only problem now is the CPAP itself is causing CA events? Or is this a case where I need to play around with machine settings and get it better tuned for me?