cpap pillow medicare

I have been on cpap for 2 weeks now, I have had 4 different masks. I can fall asleep now no problem, but am waking up during the night and taking my mask off. It is getting very frustrating as I thought that this was a magical cure for tiredness but am getting so put off over the whole thing I feel like just giving up, have others had the same type of feeling?

It takes a while to find a mask or nasal pillows that work for you. You just have to keep trying. I made several appointlements with my Durable Medical Equipment provider to go there, and try on a couple of masks before selecting one and trying it. After 8 years, I'm about to start my third nasal pillow, the Philips DreamWear. With this one, I was a 5 month beta tester some time ago, so I have prior experience using it.

I use a CPAP machine, with a nasal mask setting is 15. I do believe it makes me sleep better. However it causes serious gas especially in the morning. I know others have reported this problem but have yet to see a good answer.

I believe these 4 thing are somehow interrelated The sleep disorder place has ordered a cpap continuos positive air pressure pump with a mask. Hopefully this will solve the sleep aphnea. Re: post nasal drip: The allergist gave me 2 samples, both of them are mists. I have taken first one and then the other for 6 days now and I can not see any improvement. .Th allergist wants to put me on a long program of shots, probably years.

Cardio visit yesterday, only have to go once a year now. CPAP working better, have dissolvable zofran at bedside, as I wake up either with a headache (from straps too tight) or nausea, so grab one of those; they work almost instantly. So am sleeping better and with Adderall and better rest, am feeling much better. Can I wish away the summer heat/humidity? Not sure I will get the invite for Lemtrada as medicare requires that you have been on two other drugs at least.

If you do have sleep apnea, the treatment is that you will sleep with a CPAP machine. It stands for Continuos Positive Air Pressure. You wear a mask that blows air down your passages to keep them from closing when you sleep. Cause when they close is when you stop breathing. Id it is determined you have sleep apnea it is vital that you wear the cpap eveytime!! You can die from sleep apnea just as easily as a baby can die from sids.

I am having a hard time gettting use to the CPAP. I asked for the nose pillow when i got the results, thinking that i would like it better, It has been two weeks so i asked for the small mask. I was also told that i need to use CPAP with the water. When i wake up I find the need to take it off, then when i go to put it back I get very anxious, palpitations or it feels that my heart is racing. So i sleep without it. I have thyrothis with six nodules. had a FNA results were negative.

Hey chevy man. I've seen you around here for a long time. How about more details on the elevated pulse. How fast is it? and When does it occur? I too wear CPAP. I've used it for the last 6 years now, and it no doubt has saved me from an early, painful demise as I had very severe obstructive sleep apnea. Prior ro getting on it, I had been waking up with a pounding pulse in the middle of the night. It wasn't SVT (which I had), but an elevated and pounding pulse.

I have sleep apnea and was using the cpap machine but used it only once cause i could not at all sleep with a mask on my mouth and I could not aford to pay for it. So I returned it ,but now i cant sleep and during the day at abut after 12 noon i feel really tires and headaches and very sleepy . So i take caffine pills everyday to stay awake. I know taking pills is no the answer and I should be using the machine. My question is is there any other way to cure my problem with out the machine.

Anyone on medicare have any experience or enlightenment on provigil financial help? I've been quoted 33% copay (tier 4) by my drug insurance company which is over $300 for me The online sources I've contacted no longer cover provigil since the generic came out and the generic is about the same price... Looking for financial assistance sources if anyone knows of any thanks!

Did you try the nasal pillow or nasal cannula? The nasal pillow goes over your entire nose and the cannula goes right up into your nostrils.

Hi you are not alone i to have Sleep Apnea i also on a CPAP machine are you , I think i am the opposite to you i cannot sleep without medication never mind can't have it all nice, please feel free to drop me a note if you like once again you are not alone.........

Hi, To answer your question: No I haven't heard of the sleep study for MS. My MS specialist and neurologist KNOW I experience pretty severe fatigue and they never once mentioned to have a sleep study done. (they don't know I had a sleep study or that I use the CPAP) forgot to mention it to them... I had a sleep study done back in April, before my MS symptoms began...(I was dx with asthma.... the pulmonologist asked if I had fatigue or did I snore..

The reason i ask is because i dread sleeping now. I inevitably wake up totally blind or fuzzy in whichever side i'm sleeping on. I realize it's the pressure i'm putting on my eyes sleeping on my stomach into the pillow, i'm not totally ignorant. But i can't control the way i toss and turn at night having sleep apnea, and a very severe form of panic/anxiety attacks lately does not make sleeping a joy as it should. I actually dread waking up in the morning because of it.

I have been using CPAP machine for over a yr. now and I have seen no improvement in my sleep. I use the nose pillow mask because of me being a side sleeper but I find me waking up with my mouth open and sometimes there is drool. Should I try a full mask to see if that would be any better for me?

Have Herpes of the mouth, and awhile back had a pretty bad break out, it spread to the inside of my nose. Now there seems to be a scar there, it hurts me whenever its touched inside and or out. I have sleep apnea, and sleep with a cpap, the kind that shouldn't hurt the nostril pillow. However this does hurt me, even the air hurts. Is there anything I can do? Is it best if I try an on the nose mask?

Just wanted to add that my nurse practioner that works with my MS Dr. is going to get me into see one of the pulmonoligists at UCSF ..this makes me happy. There are not many of them around, at least good ones.

I have just visited a prosthodontist concerning a device recommended for mild sleep apnea patients instead of the CPAP machine. Medicare will be billed $800 + and I will pay $4-500 for things insurance will not cover. ON THE OTHER HAND: www.snorerx.com/stopsnoring looks very, very , very much like the device mentioned above that I am NOT going to have Medicare billed for. Why not invest $100 and try it instead of draining Medicare and spending much more myself? I have mild (5.

Hi, thanks so much for your response. I'm on Spiriva and use a Nebulizer with Albuterol. I have a rescue inhaler for my asthma. I did have a weeks course of Prednisone about 3 or 4 weeks ago when I had a bad spell. I don't want Advair as I used it for a couple of years for asthma before the COPD was diagnosed and didn't see any benefit from it at all. Hopefully my doctor will help me find a way to improve a bit.

I have used a cpap for 10 months. My most prevalent problem is that the exterior of my nose tickles as though a feather is being brushed against it. I use a full face mask most of the time. I have tried applying Vaseline and various other moisturizers to no avail. The only thing that has seemed to help to a limited degree is "AquaPhor" daubed on my nose, not rubbed on.

In my case it showed periods of low oxygen levels, sufficient to qualify under Medicare (yes I have insurance) for supplemental oxygen. I discussed with my primary care doctor and ended taking an overnight sleep study at the local hospital (not low cost) and was diagnosed with mild obstructive sleep apnea...

I have a CPAP machine on a months trial, this is one that varies the pressure as required it records the information on to an SD card so when I return to the clinic I will then be given a machine that has the correct fixed pressure. I have a full face mask as I could not get on with the nose only one. Now my problem is I wake in the middle of the night with a very dry mouth (i mean completely dry) my mouth has ballooned with air and the mask is vibrating against my face.

I changed my pillow protector and I thought my problem was solved but I still wake up with a stuffy nose. Could it be my sleep apnea machine? Or something else? I'm fine once I'm awake and I go downstairs.

Cpap pillow medicare

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