I’m a paraplegic with OSA. My belief is that the inspiratory phase is so fast, even the slowest setting is 600 ms (.6 of a second!), that it causes a spasm in my body and thus the more wakeful events. I’m more tired using a BiPap than without. Any suggestions? TIA.
I have never used the device you have, but I can relate my experience with OSA to you.
I was diagnosed in 1986 with OSA while I was still on active duty in the military. As a result of the diagnosis, I had UPPP surgery removing my tonsils, adenoids, and part of my upper palate in an effort to treat it. The UPPP surgery failed.
I had another sleep study in 2006 with OSA again diagnosed. This time, the VA supplied me with a CPAP machine. Due to PTSD from military service, I could not deal with the CPAP either, and I gave up.
Last year, my other half insisted that I do something to keep me from stopping breathing in my sleep. She couldn’t sleep at night for fear I wouldn’t start breathing again. Loudly obnoxious snoring wasn’t any help either.
In December, I had a sleep study at the University of Michigan hospital. The findings were the same, OSA. My REI was over 50, putting me in the severe category.
The otolaryngologist at U of M (who shares his time with the VA hospital) recommended a device called “Inspire”. It is an implant similar to a pacemaker that stimulates the hypoglossal nerve that moves the tongue. You can turn it on and off with a remote control.
For me, it has been a life changer. No more breathing stoppage, no more snoring.
Your doctor should be consulted, before making the decision.
Here’s a link:
Have you discussed this with your physician? Maybe you can get more useful info there.
Shouldn’t you talk to your doctor or BiPAP technician?
I don’t some people do and fair well. Talk to your physician and don’t be afraid to try new things.