I snore really loud, wake up with dry mouth.
Headache at back of head and top of head.
This has been going on for a while.
Doctor said i dont qualify to be tested for sleep apnea, as he did a questionnaire and said as i dont fall asleep during the day, he cant send me for further test.
Must confess, this isnāt something Iāve investigated before as thereās enough going on as it is! However, I meet the profile for both OSA and CSA on a number of fronts. This article: Sleep Apnoea and MS makes for interesting reading. Time I spoke to my MS Team and GP. Not sure who would have primacy on this one?
Iām in the US, and we do a lot of things differently here, but Iāve never heard anyone say that āfalling asleep during the dayā is a requirement for having sleep apnea! Is it possible to find another doctor?
My son and I both have CPAPās now, and theyāve made a world of difference in our sleep.
I know the US healthcare system has a world of troubles of its own - massively expensive and astounding poor value for money by global standards, for starters - but it is surely not quite as rubbish as the NHS at preventative medicine, which the NHS is often hilariously uninterested in (as in this case), despite its straight-faced claims to the contrary.
Some time ago, before being diagnosed, I suffered from some frightening symptoms that cleared after I was given prednisolone. My airway, chest and nose felt totally clear, but during the day I would feel like I just wasnāt quite getting enough air and felt the need to take a deep breath now and again throughout the day. At night I would wake up gasping several times, like Iād somehow forgotten to breathe. I would wake up with a banging headache and feel very groggy. It was very frightening and at the time they put it down to panic attacks, stress and anxiety. I really felt robbed off by everyone I spoke to. One day I went to the walk in centre in desperation convinced that if someone didnāt do something, I might die in my sleep. The nurse gave me a small and short course of prednisolone thinking that I could be having an allergic reaction. It was 4 tablets a day for 5 days. On the 2nd night I didnāt wake up and slept soundly. It came back once after that a few months later, had prednisolone again, and (touch wood), Iāve never had it since.
Itās also worth mentioning that I also suddenly suffered from extremely dry eyes at that time, that lead to them being horrendously blood shot and an ulcer and slight difficulty in swallowing. I was told that the problem with my eyes was just āone of those thingsā and I would need drops for life. Swallowing was also put down to stress, anxiety etc. Both of these issues cleared up too and have never been back.
Since being diagnosed, I have asked several medical people about this and they have categorically said that it was NOT due to the MS. Now Iāve read that article, I wonder why they are saying that still?
I now know that I have two tiny lesions on my pons (an area that deals with regulating breathing, tears and swallowing) and wonder if that was what was happening at that time.
I was diagnosed as having sleep apnea 2 years ago i do go to sleep in the afternoon everyday which i cannot help.
I was given a cpap machine but i cannot use it as when i was born very premature i had to use a cpap machine as a baby and it makes me chlosterphobic i cannot wear the mask.