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I just keep water by the bed to take a drink.
Life can be amazing - enjoy it one little victory at a time http://kats-losing-it.blogspot.com/
Also if you tamper with the machine and there is a problem ... insurance may not pay for the repair or replacement.
As far as the dry mouth from mouth breathing goes ... I know this will sound silly but get a chin strap. I wore it for the first 3 weeks I was on the bipap and it trained me to keep my mouth shut when I sleep.
I have been on the bipap now for 6 years and I couldn't sleep without it. I love my machine :)
Life can be amazing - enjoy it one little victory at a time http://kats-losing-it.blogspot.com/
Life can be amazing - enjoy it one little victory at a time http://kats-losing-it.blogspot.com/
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Good luck.
I have the allergies under control now after many years of experimenting with treatments. I am told that once I get to where I can use the CPAP all night and sleep I should be fine. For now I am on PRVigil for the tiredness. It has helped a lot. I do need to take more time to be sure the machine and hoses are clean everyday.
Thank you for all your help. I will check with my doctor to see if there are any local support groups.
You definitely need to see an allergist and not give up until you get the right medication for your particular needs. Don't be intimidated by the doctor but simply let the doctor know what you've tried and what has happened as a result. I've gone through a number of sprays, pills and inhalers and have used them singly or in combination. Different times of the year require a different regimen. I suggest that you keep a daily log for a year so that you know what's going on during the different seasons. (A room humidifer would probably help, but you must be sure to keep the tank clean and free of mold.)
You should also be sure that the water reservoir, tubes and mask of your CPAP are kept immaculately clean. You could be infecting yourself with mold if it is allowed to grow in the tank and/or the tubes. Clean it with plain white vinegar on a daily basis. Also, make sure that you only use distilled water in your reservoir.
There seem to be a number of apnea doctors in your area, and I would check with them about a support group. The place where you were tested should also have information.
Please feel free to contact me if you want to "chat". Also, take a look at these links to see if they're of any help. Good luck.
I will have to see if there is a support group in this area. I have not heard of one.
Thank you so much for the information! This is so new to me and with surgery coming up within a couple months it's a little overwhelming. Good info. I'm going in this morning to get my VPAP, so it should be interesting,