LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Anyone use a CPAP machine???

 - UBBFriend: Email this page to someone!    
Author Topic: Anyone use a CPAP machine???
merrygirl
Frequent Contributor (1K+ posts)
Member # 12041

Icon 1 posted      Profile for merrygirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
I started using my CPAP machine 2 nights ago for my sleep apnea. I am not sure if it is working.

Last night I woke up and had ripped it off in my sleep....


how do you deal with it and does it help?

Melissa

Posts: 3905 | From USA | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
doc
Member
Member # 14471

Icon 1 posted      Profile for doc     Send New Private Message       Edit/Delete Post   Reply With Quote 
I got one . Works for me . try to strap it on tighter . or look into a differnt style face mask as they have many. Doc
Posts: 95 | From nys | Registered: Jan 2008  |  IP: Logged | Report this post to a Moderator
sparkle7
Frequent Contributor (5K+ posts)
Member # 10397

Icon 1 posted      Profile for sparkle7     Send New Private Message       Edit/Delete Post   Reply With Quote 
My boyfriend uses one & he does that all the time. I don't know what the answer is, though.

I asked him, like, 500 times to look into getting a different mask. Sometimes men are stubborn about that sort of stuff.

I think it's difficult using a CPAP. My boyfriend does seem to get better sleep when he uses it - even if he does remove it during the night.

Posts: 7772 | From Northeast, again... | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 9 posted            Edit/Delete Post   Reply With Quote 
i tried for 3 months; quit it because my different masks would wake me up seeping out air from sides of my face.

also humidifier which was supposed to help, made me worse ... felt 32 degree water coming into my face vs. 80 degrees! [cussing]

IP: Logged | Report this post to a Moderator
klutzo
Frequent Contributor (1K+ posts)
Member # 5701

Icon 1 posted      Profile for klutzo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I got a swollen, prickling rash from the mask blowing air on my skin, and could not stand the way it leaked, since I am a side-sleeper.

I switched to a nasal pillows system called The Breeze, which does not involve a mask at all, and was able to be 100% compliant right away. What a difference, at least for me! I have been using it for a year and a half now.

My muscle pain was much worse at first, because I was sleeping so deeply that I was not moving at all, but that went away once I caught up on deep sleep. I was so deep sleep deprived that I had no dreams at all for the first couple of months.

There are CPAP forums on the net where people with experience, just like we have here, can help you deal with problems like "rain out", the humidity problem Betty referred to.

"Rain out" can usually be fixed by lowering the setting, and/or warming up the room, and/or using a special heated sleeve on the tubing, etc.

It was a CPAP forum member, who runs a DME himself, who told me about the nasal pillow system, so if I had not gone there, I'd be a CPAP failure.

It's made a huge difference in the depth of my sleep, and in my energy level. On many days I can keep going all day long now, almost like a normal person. I would not want to be without it.

You have the right to try different headgear until you find something that works for you, so if I were you, I'd call my DME supplier about it. Good luck and hang in there....it's worth it.

Also, untreated apnea increases your risk of diabetes, your stroke risk is 400% higher, and your heart attack risk is 500% higher,a good motivation to keep trying.

klutzo

Posts: 1269 | From Clearwater, Florida, USA | Registered: May 2004  |  IP: Logged | Report this post to a Moderator
Boomerang
Frequent Contributor (1K+ posts)
Member # 7979

Icon 1 posted      Profile for Boomerang     Send New Private Message       Edit/Delete Post   Reply With Quote 
Have never heard of "The Breeze"...is that something you get from a doctor?
Posts: 1366 | From Southeast | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
B R H
LymeNet Contributor
Member # 12159

Icon 1 posted      Profile for B R H     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have a FART machine. Oh, sorry, I thought the subject said CRAP machine. [Smile]
Posts: 246 | From Grass Valley, CA | Registered: Jun 2007  |  IP: Logged | Report this post to a Moderator
amk33
LymeNet Contributor
Member # 13206

Icon 1 posted      Profile for amk33     Send New Private Message       Edit/Delete Post   Reply With Quote 
That is really funny! [bonk] At first glance, I thought it said "crap", too.
Posts: 418 | From NJ | Registered: Sep 2007  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.