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There was a great but sad posting on this site from a woman who had lost her husband with OSA. You need to find it and have him read it, it may motivate him to care more about his therapy. I have known couples that got divorced because of non-treated OSA and snoring. It is serious and you have ever right to be concerned. best of luck to you and my prayers for change will be with you.
I think the stuffy nose is due to the change in mask. I had 2 days on that mask and I thought "Wow this is great, I actually feel a little better". I usually wear a Mirage Quattro full face mask due to mouth breathing. I think I have, after 2 years of this, trained my brain to keep my mouth shut. Now if I could only keep it shut when someone is talking to me, I'm always interrupting because I'll forget what I wanted to say if I wait. LOL (Apnea related I'm sure).
So things were going fine with the nose only mask and then...the plugged nose. I have not had problems for some time now because of using Flonase nose spray and using a Netti pot each night, well, most nights anyway. My guess is my nose is not used to having ALL that air in a jet stream up the nose. I have switched back to the full face but, now it's bothering me because the other one was soooo comfortable! I'd like to use the nose only mask but how can I get used to the mask when my nose plugs up and I'm forced to open my mouth. I don't know, sometimes it's so hard. I saw light at the end of the tunnel and now I'm in the dark again.
I've always used my humidifier and it was kind of funny, but not, on my first night with the nasal mask when I turned over in the wee hours of the morning I got a rude awakening with an unintended nasal rinse! Yuck! I'd never had a problem with condensation before. I made a hose snuggy for the foot long tube attached to this mask and solved that problem.
About camping, your comment about the storm is a nice way to think about it. Thank goodness it's over and it was only for one night! I hope you are able to get back to camping and canoeing soon Susan. Good luck.
PS...Wallace and J. Thanks for the concern. I don't think he wants to understand just how much danger he puts himself in. I need to talk to him about life insurance. Hmmm, I wonder if having OSA makes it harder to obtain life insurance.
I don't know how much those batteries cost, but I bet someone on here does. Mike, probably, or Rock or one of the other professionals--they're a wealth of information just sitting around waiting to be asked!! My therapist is on CPAP, has been for years, and he uses a boat battery when he's out and about like that!!! But there are special ones just for our equipment--that's what I'm going to get as soon as I feel ready to go out camping/canoeing again which is one of my most favorite things to do!! Not ready yet though. I just remembered, Mike has some connection with an apnea supply company--he could probably point you in the right direction. Again, just a thought. I've seen them on the internet in my apnea travels in cyberspace--don't remember seeing $$ though. You might check there too and see what you find. There are different kinds...
Susan McCord :-)
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