Cpap gives me gas

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cpap

sometimes i feel fine i think im over what ever it is , then i wake in the night feeling nausea, light headed, wierd sensantions through most of my upper body and back, i feel stabbing pains and sometimes i can actually see movment in my chest from gas passing through me. I feel asthough every breath i take is like breathing some toxic gas it does'nt feel like im breathing normal air . Seems to happen no matter what i eat and it seems to always hit me during the night.
This may sound very unususal,and beleive me I wouldn't even mention it, if it hadn't become such an anomoly to me. For the past 3 months or so I have noticed that I have gnats flying around me at home. Just a couple,but they follow me from room to room, wherever I go. They also follow me to work,and I have them in my office too. Then when I go to another person's office, they follow me in there too. So essentially it's me they are after.
As an ear, nose and throat specialist with years of experience helping people breathe better through their noses, I have seen hundreds of people have dramatically improved lives. One of the most important reasons to breathe through your nose is because of a gas called nitric oxide that's made by your nose and sinus mucous membranes. This gas is produced in small amounts, but when inhaled into the lungs, significantly enhances your lung's capacity to absorb oxygen.
There are several online groups that also have interactive activities, as in one person makes something and swaps it with another..I have met many great people, and it gives me something I feel is purposeful to do. Maybe there is a new or past hobby waiting for you to discover and enjoy?..I often quilt or embroider at night, when insomnia is bad...and online groups also don't have the typical daytime hours..easier to find a good fit for yourself. I hope things get better for you!
Weird. The neurologist told me that neuromuscular disorders like MS can cause breathing problems in people with MS. Has anyone ever heard of that before or experienced it yourselves? I thought I was just having the MS Hug all the time that was causing my breathing problems.
will just tell me to come back to KC and see them, and then they're going to tell me that there's nothing that they can do for me. I was reading online tonight that it might take up to 6 months for a person to get better after a relapse...but hell, is a person suppose to get worse?? Because I walk very very slow...like an 80-90 year old person would walk...I am only 31 and this is really starting to scare the heck out of me. Also, I am on Copaxone and have asked the dr.
My doctor thinks I may be dehydrating in the heat and suggested I drink more water before he gives me another prescription. I am hoping this works as I would hate to go through the side effects again. Do you have any suggestions that I could bring to my doctor if the symptoms do not dissipate? Thanks for your time.
Blood work also done, was called later by Dr told toreducce lupron to 5 units fri night and add 200 dial up of Folistim and 10 units of solution x ( of which dr said he cant tell me what it is or he would have to kill me) lol ( I told him you already tried in June... remember lol ) I think the solution x is sodium chloride but it is written on with a black marker....... hmmmmmm that one throws me for a loop I wonder why that was delivered with all the rest of my meds by cvs caremark?
I get a sore throat (not tonsils but when you swallow) I now go straight on antibiotics and use Bricanyl inhaler although it doesnt seem to have much effect except to cause alot of mucus coughed up from the lungs. It causes me to have spasm coughing and if I cannot control this to 3 or 4 coughs my windpipe closes over making it hard to breath in or out. The last one about 2 years ago stopped me breathing in and out completely for 10 to 15 seconds and I thought I had bought it.
Me too-exhaust. I thought I was losing it!! This just stumps me. It wakes me up at night. Could it be some kind of acid reflux i wonder! Glad to know I am not alone!
It lasted for days and hurt when I breathed (particularly exhaled) It hurt to lay on that arm and to lift it but it definitely didnt feel like a muscle spasm. It was on the outside part of my arm/shoulder. Sometimes physical exertion gives me similar chest/arm pain especially if I walk a lot in the cold or am outside shoveling snow.
Not my fault that I had to snicker at the last line there because every time I talked to my Doctors (plural) about medications and side effects they told me that Tramadol was NOT the problem. Then there was usually another drug put on top of that Tramadol. And they told me to take more. I always thought it was the other drug, not the Tramadol. Yeah. I was wrong. It makes me very angry that these Doctors know and aren't telling people. I don't believe that they are ignorant.
This gave me much information and I am now doing stretches to help. The hernia gives me terrible reflux and I use Hydrochloric Acid to calm this down. ( Antacids should not be taken for the reflux. I was told by a Naturepath that our stomach needs more acid to digest food. The "purple pill" and others take acid away does only harm to our body.) I read from an article at Google that the hernia can also cause one to have difficulty swallowing...another symptom I have.
It seems like an every 10 yr thing for me. I have been diagnosed to having mile sleep apnea which I have a Cpap machine, but as of a month or so ago I started having an attack in the middle of the night I would wake up gasping for air, my heart would be 130-150 beats a minute and my blood pressure was off the charts. I was certain I was having heart failure. I have been to so many damn doctors and Emergency Rooms and everything comes back just fine.
The pain is so bad I yelp eveytime I try to move. If anyone has any tips please fill me in.
I just thought I was a bad driver...My oldest son ran into a gas station and called his father. No keys for me after that...and no I don't drink...lol While I was approved for SSDI, I have a two year wait period before I can get Medicare. I began receiving SSDI in September. They have said I am eligible in July of this year??? SSDI sure counts differently or uses a new math program. So, I guess I will wait. I would love to have PT but can't bring myself to ask favor again of my husband.
I'm wondering if I have a pinched nerve in my upper back which is causing all of this, since this area gives me more pain every day. I also notice much of the pain disappears after I sleep, or lay down and relax. Anyway, I'm going to see my GP in two days. We'll see what else he can do for me.
I'm a 60 year old men, in excellent health, except for experiencing tremors during sleep that wake me up and have difficulty going back to sleep. As I start to fall sleep again, I feel these "rumbleling" (tremors) around my upper body. I immediately wake up again. These tremors last for about 10-15 seconds after I wake up. The first time I experienced this condition was exactly two years ago. It lasted for about four days and it simply went away.
Been to er several times, and yeah just pain killers. Some even tell me it is gas I do not think so. I do not know what to do. I am scared a lot of the times.
is taking a small amount of Buckley's cough medicine. It seems to open up the airways faster and gives me a small peace of mind that I have help.(does take your breath away for a few seconds, but usually when I feel the tickle, lose of breath is not far away. ) It doesn't work as well for the ones triggered by a cold, but it is great for the other times when it "just happens." Buckley's has saved me hundreds of times. I take it everywhere I go. Running, skiing, everywhere.
The doctors still think I'm imagining it but one day I'll find one who takes me seriously and we'll figure out exactly what causes it. Thanks again and I hope you stay well.
A few weeks ago my OB signed off on me but told me to see my family doc because my bp was going up. I watched my bp at home and we found that it would get high anytime I go to the office. I'm really hesitant to go back there! But I'm sick of feeling so incredibly bloated and FAT. I've been trying to lose weight since my 5th child 2 years ago and all of a sudden all my hard work has flown out the window. This is ridiculous!
During my last visit the doctor suggested more excersize to me, but it didn't seem to give me any relief. I am interested in hearing your progress with these symptoms since I am going through the same thing.
So everyone thinks 3 or so PVC's a minute are nothing huh. That gives me a bit of confort I guess. I don't really even get that many but sometimes it acts up and does start at three or so a minute. I have always read that if you have more than 6 a minute you should go to emergency. When it does act up and does one every second or third beat I always think this is the end I guess. I would give ANYTHING to get rid of these. I don't believe the cardios when they say nothing is wrong.
the 3 newest nodules have come after I quit smoking. Drs tell me not to worry, yet cannot tell me the cause of these nodules or even what they are......Any suggestions? Im going crazy wondering..... Thanks in advance!
This also happens to me. At first I was a little bit worried. After a while, I realized that nothing would harm me, and that they would go away. Usually I wake to see spiders crawlig on the wall. The first time it happened, I got scarred and closed my eyes. After I opened them again, it was gone.
What other medications do you take along with Topomax.Has you family noticed any differences in you? On that note let me introduce myself.My name is Davette.I have been on Topomax about 31/2months.I have migrains and seizures.I have been extremely effected by the side effects.Mostly memory and spelling.I have tingling in the fingers and toes.I also have little appetite and have lost 17lbs.Witch is great for me. I am over weight.I am tired more than normal,but i did sleep alot due to migrains.
Every time I blink, my eyes go off in different directions giving me double vision. Shaking my head violently gives me about 5 seconds of clarity before things start going fuzzy again. Also happens to me on airplanes and boats, anything with that low bass vibration. If it is a blood preassure thing, would High-G Training do anything? Forcing the blood to your brain? I'm going to take off my shirt before I travel home to see if it is something where the collar is preassuring my neck.
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