CPAP Intolerance
Over the years, I have had two separate sleep studies. Both were absolutely horrible experiences. I have insomnia anyway -- since childhood -- so that equipment simply made it horrible. I was freaking out. I think about 4:30 AM on the last one, they broght me some ambien, so I may have dosed a little bit between 5:00 and 5:30 AM, at which time they annoucned the study was over. Both studies said "severe sleep apnea". Of course, I don't know how they could diagnose that on about 30 minutes of sleep. Anyway, on both occasions I tried hard to use a CPAP for weeks. Those were about the worse 4 months or so of my life. Conclusion: If you want me to sleep any, I do not use the machine. If you want me to use the machine, I will get far, far less sleep than using it. I just cannot imagine how anyone can tolerate them? I have tried various masks including the little nose pillows. I find a comfortable spot and I feel air blowing in my eyes, which causes me so much anxiety. I was shamed -- terribly shamed -- by providers when I would tell them that I just cannot do it. Every single proivder now asks me about it and feel like they need to read me the riot act about what may happen if I don't use it. Nobody understands the situation -- nor do they try. Yes, I am extremely tired many days, but less tired than trying the machine and getting so worked up about it every night. And, they wanted me to take it when I travel ?!?! Nope, not going to happen. Ever. My memories of wearing the mask -- "I cannot wait to get this thing off so I can get a little bit of sleep". Frustrated as can be here.
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I have been using Vicks vpor Rub in my nostrils...helps a lot!
Hello, I use a CPAP machine and have been trying to get use to a mask when I broke out and ended up with a staph infection on my face. I understand the whole law thing and I am told I cannot be qualified for a new mask refit of any kind until april 10th which at that time my doc already sent a script for a nasal pillow do you know of any way to receive it earlier besides a lengthy insurance type appeal?
I had two sleep studies and I also tried two different cpap masks at home. I had some of the same experience. I slept less and was more stressed with the mask. It would blow air in my eyes and at times would wake me up with a big gust of air making my cheeks blow out like a chip monk with nuts in its cheeks. It also squealed and woke me up as I rolled over on the hose. I also have to go to the bathroom frequently and every time that I got up, I had to undo the hose and then refasten it again. When the mask with the parts that went to the nostrils would slide over, it would stop my air supply. I have had extensive nose surgery since then for 3 things that could have affected my breathing and should have been looked at prior to sleep apnea tests. Those things were a 90% deviated septum, a swollen turbinate that blocked air, and collapsing nostrils from deteriorated cartilage with aging which required plastic surgery to have the nostrils stay open. I didn't realize I had those conditions and they tell me my nose is still healing so that's all I know for now. I do think I am breathing better than I was.
Go to different doctors until someone listens.
@tbaxter33 -- thinking of you and the CPAP that just did not work for you at all.
I recall you mentioned you felt the doctor shamed you over this, which would sure feel terrible. Did your doctor ever present any alternatives? Have you found any in your research?
I was told that my bipap was set on 4 but I'm not sure if it is. I feel like too much air is being forced in me after the ramp period is over. I have the Res med 10. Also I have bloating and have gained a lot of weight. I was actually hoping for the opposite result. Could the machine being set on too high of a pressure cause this. I am great during my ramp time but when it switches to the overnight pressure it seems like it is too strong.
Also I have the heated tubing which I keep turned off and I keep the humidification turned off as well because it is very humid in NC most of the time. I still seem to retain water terribly since I started using this machine. My ankles swell and of course the docs all say it doesn't cause that but people I have talked to say that it does. I have been using this for 3 years now. Does anyone else have these problems??
Hello @andreadawn, Welcome to Connect. I have had the too much pressure problems in the past and was able to adjust the pressure after talking with my sleep medicine doctor and care team. I also don't use the heated tubing or humidifier tank because it seem to make my congestion worse.
Here's a YouTube video that explains how to check and change the pressure.
-- How to Adjust Pressure and Settings on ResMed AirSense 10 Autoset CPAP: https://www.youtube.com/watch?v=fcPp1i0XuYU
I wouldn't think the water retention and ankle swelling would be related to using you CPAP.
Have you discussed your ankle swelling and symptoms with your doctor?
I see most of these post are from 2018! I have been diagnosed with Obstructive sleep apnea since 2014. I have had the same problems that have been mentioned above. I need a full face mask and tried many before I found what worked or at least was better than others. I had a second sleep study which confirmed the OSA with a change in pressures as events had risen. I then had a third sleep study and was diagnosed with Complex sleep apnea which means I still have OSA and now central sleep apnea. I absolutely have to sleep on my side and NEVER on my back. My events go up considerably if I end on my back somehow. I could go on and on with the problem but what I want most is to be able to chat with someone else who has Complex Sleep Apnea to see how he/she has overcome some of the problems I have.
Welcome @merrilyzi, Here are a couple fairly recent posts from member discussing complex sleep apnea in other discussions:
@kb1942 shared their experience here - https://connect.mayoclinic.org/comment/333412/.
@tacitsentinel shared their experience here - https://connect.mayoclinic.org/discussion/how-do-i-keep-blood-pressure-in-check-with-dysautonomia/
Here is the search results with links for members who have posted about complex sleep apnea: https://connect.mayoclinic.org/search/?search=Complex+Sleep+Apnea&pg=2
Since you also mentioned having central sleep apnea you may also find the following discussion helpful -- Can a CPAP machine treat central apneas?: https://connect.mayoclinic.org/discussion/can-a-cpap-machine-treat-central-apneas/
I also have to sleep on my side and wear a full face mask for my OSA. My events will go up if I sleep on my back. Have you discussed your symptoms/problems with your sleep medicine doctor or care team?
I'm trying to find out as much info as I can on my own as My Primary MD knows little about Complex sleep apnea. My ENT tried 2x to reduce my Turbanines unsuccessfully and recommended I see a Neurologist who specializes in sleep apnea. Appointments are few and far between. My sleep Doctor covers a large area and is difficult to get ahold of. I have never been told I could control my own pressures. If I call about an increase in events I have to take my machine into a supplier. Raising the pressures never seems to help much. I am always tired. I was hoping to chat with someone who conquered Central Sleep Apnea with use of the machine and good fitting mask and sleep positioning. My problems would be solved!