Sleep HQ isn't giving me access to your charts, but given what you've said about them, I see absolutely no reason for you to stick with the changes you've tried out. Your AHI and FLs are worse with these changes, so go back to what was working better for you. Side note: Often when people turn EPR ON...

Yes, bumping your EPR up sounds like a good next step. You're still pretty new to PAP therapy, and sometimes it takes a while before it provides restful sleep. So I'd recommend you have some patience and see how things look a month or two from now. There's a decent chance you'll be feeling better. I...

Well that's encouraging! Stick with these settings for a few more nights and see how it goes. The next step I would probably recommend is to re-introduce some EPR. That will give you a lower pressure when you exhale (except when you're at 4), which might help with the residual aerophagia issues.

That's it; the change would give you more information. Who knows whether the information would be helpful or not; it'd have to be available before anyone could figure that out.

I hope you'll follow up on the periodic limb movement issue.

In at least some places, the CAs seem to be part of a pattern of unstable breathing. Deeper breathing (perhaps as part of an arousal) leads to a CA, there's some deeper recovery breathing after the CA, then the deeper recovery breathing leads to another CA, etc. You can also see some waxing/waning p...

I’d suggest you go ahead with the increase to 7 as your minimum. We can then take that as a starting point for any further adjustments. Occasionally it will make sense to cap pressure below where it “wants” to go, if it’s mostly being driven up by flow limitations and if pressure increases are probl...

I think your best bet is to keep a written record for a couple of weeks that notes your answers to something like this list of questions: How long did I sleep last night? Did I wake up early and feel like getting up? If yes, did I go back to sleep for some additional "lighter" sleep? How did I feel ...

Welcome! In so many ways, you're off to a great start. You're sleeping with the machine, you have leaks under control, you're using Oscar, and you're taking an active role in making your PAP therapy work. Sleep is highly variable from one night to the next, so when you make changes to your settings,...

Your flow limitations may or may not be contributed to unrestful sleep. The best tool you have to reduce FLs is EPR. It drops your pressure when you exhale; by the same token it increases pressure when you inhale. This little increase can help reduce FLs if they originate in sagging tissues in your ...

As you may already know, IGA nephropathy can cause tiredness as a symptom. Are you seeing a kidney specialist? Are you receiving any forms of treatment for the disease?

+1 Zonker. One way raising your minimum to 7 might help is by giving you more consistent flex. (The lowest pressure the machine can generate is 4, so you get no flex at 4, just a little at 5, etc.) Flex can sometimes help with flow limitations and hypopneas. After you try that for a few days, you co...

About your sleep position: You might want to try this for stomach-sleeping:

wiki/index.php/Sleep_Positions

For some people who use CPAP, this is a big help.

I had some thoughts about this, but on reflection I think the prior question is whose requirement you're needing to meet.

You might want to check that you don't have ramp on with a low pressure, which can leave people feeling air-starved.

Change the mode first; then use the settings I gave you. Any chance your doctor could work with you on changing the timing of your diuretic pills?