Hi
Just to let you know that all is going okay with the CPAP
I had to change the mask the other day as it was uncomfortable,but have a better one now which is okay.
It feels really odd wearing this hideous mask in bed ( or whenever i want a nap ) because whenever i have an 'apneoa' the amount of air going through the mask increases as it automatically detects it..and the power can only be described as putting your head out the window on the motorway
It also leaves me with an INCREDIBLY bad dry mouth...my inside of my mouth literally doesn't have any fluid and is very uncomfortable...At which point i have to take the mask off,have a drink then put it back on but reset it so the air going through is at the minimal amount.
Still...i have it more or less for life so i should get used to it
On the good side though it registers how many times i stop breathing in an hour...and it ranges between 2 - 5 times ...a bit better than 70 times an hour before i got diagnosed
Also my blood gases were tested and are now 96% . . the lowest i registered was 50% leaving me high risk of having a stroke or heart attack in my sleep
I'm seeing my GP on Thursday to discuss it more so i'll let you know if anything changes.
Take Care
Andy xx