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[CPAP] New: I’m struggling very badly
#11
RE: New: I’m struggling very badly
I'd suggest you turn off the ramp feature, which is preventing you from having the full benefits of EPR during the ramp period. Did the new settings make any difference to your chipmunk cheeks?
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#12
RE: New: I’m struggling very badly
(05-08-2023, 12:01 PM)Dormeo Wrote: I'd suggest you turn off the ramp feature, which is preventing you from having the full benefits of EPR during the ramp period.  Did the new settings make any difference to your chipmunk cheeks?

Yes, the new settings did help with the excessive air in my mouth, but I do not think I fell asleep for the 3+ hours I had the machine on. I will try turning off the ramp. I do feel like I'm making some progress but it's slow going.
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#13
RE: New: I’m struggling very badly
Do you have a sense of what prevented you from falling asleep? Is that a common problem for you?
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#14
RE: New: I’m struggling very badly
I'm thinking it's the mask. This is the full face mask and I could feel air blowing into my eye even though my seal was good. I am also not a great sleeper and this whole thing is causing me major anxiety.
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#15
RE: New: I’m struggling very badly
(05-08-2023, 12:28 PM)Muhlyssa Wrote: I'm thinking it's the mask. This is the full face mask and I could feel air blowing into my eye even though my seal was good. I am also not a great sleeper and this whole thing is causing me major anxiety.

Could be air from the vents redirecting off your pillow, duvet, hand/arm or whatever - place your hand over the air vent and follow the air path it's taking, then try to avoid anything being in the way of it. Sometimes hanging slightly off your pillow, or placing your head further down the pillow may help this, if that's the reason you're feeling the air in your eyes anyway. If it's a mask leak, adjustments, mask liners (google cpap mask liners) or a nasal mask with tape may be in order. 

One thing I will say is, once you're used to CPAP and you're feeling the benefit each day, you'll struggle to sleep without it. It's very familiar, the drone of the air/mask, your brain will learn it's sleep time. It just takes some time, and having good therapy that you're confident and happy with will help with that.

Uncontrolled sleep apnea is no joke, even mild - especially if it's effecting REM - will send you to an early grave with all sorts of implications from obesity, diabetes, dementia, cognitive and cardiovascular effects, high blood pressure.. it will take time but it will slowly and accumulatively  destroy your health, life and happiness.

Once you're happy with how things are progressing you'll feel differently about it all I can guarantee you!
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#16
RE: New: I’m struggling very badly
I'm here with an update and to thank those who chimed in. @Apnea23 @Dormeo @stanleyjack

The RT suggested I switch to the medium size of the full face mask. I recently took my machine on vacation to Hawaii and had really good nights with my CPAP machine and mask combo. The main difference was the hotel had really flat pillows (and probably just generally being relaxed and on vacation, plus getting more exercise than normal). 

When I got home, I switched to a flat pillow and have had some really good nights. I think I'm on my way. It has taken about two months, three different masks and two follow-up appointments with the Respiratory Therapist. 

I don't love my machine but I don't hate it either. Because I wasn't snoring or having daytime sleepiness prior to my diagnosis, I'm not seeing a huge difference in my quality of sleep but I know ultimately I'm doing what I need to do.
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#17
RE: New: I’m struggling very badly
Ah, the Hawaiian vacation solution!

So glad to hear you're on the path to easy and effective PAP use. You're right, it's what you need to do to stay healthy over the long run.
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#18
RE: New: I’m struggling very badly
Right? I mean Hawaii vacations solve many problems!
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#19
RE: New: I’m struggling very badly
Hi, I have been on an APA for six weeks. I had the same problems with air filling my mouth and my checks then popping out my mouth, and waking me up. I am not a mouth breather, but in desperation, I started to tape my mouth, and it worked for me. It keeps my tongue up on the roof of my mouth. I use it for both FFM and NM.  The chin strap did not help. I also wear a soft neck collar.

I hope this helps.
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