I have had this for ages but just got my diagnosis. I am hypermobile and believe the two to be linked. My ENT said he had never seen anyone able to move their soft palate at will like I can...! Anyway, it's pretty bad- can't sleep, tired all day, have NO short term memory at all, wake up as soon as i fall asleep. Everything is suffering. As my results were so bad (65 episodes per hour) they are going to try and get me a CPAP asap, although my sleep test was in September, so it's taken 5 months to even see anyone. Has anyone here had sleep apnea, and what did you do to help solve it?
You are quite correct in that there is an increased incidence of OSA and hypermobility and that the first line of treatment is CPAP.
No, I have never had sleep apnoea, but have been involved in it's treatment over the years.
Thank you - yes I want to try it as soon as they give me an appointment, but I worry that it will take months! In the meantime I am totally spaced out from lack of sleep, jittery and can't focus on anything. Are there any other things to maybe try in the meantime?
Yes it absolutely would I am certain. I lost weight last year and it got better. And then Christmas... the test I had was when it was at its worse. But it has seemed to come back since Christmas so I am on it again.