kreesti wrote:Thanks for the picture. I am going to need to use moleskin on my mask as well, for the same reason. I appreciate your picture for use as a reference.
My guess is that there is some kind of friction from the mask (as opposed to pressure), or friction exacerbated by pressure, but I don't know why... this seems to be one of the few consistent complaints about the mask. Hopefully there will be some sort of design change or solution.
YW re: the picture. I have mixed feelings about a redesign of this mask (since it's working so well for me overall) - with the exception of an easy-release clip on at least the neck strap. THAT would be a good thing.
sleepngo wrote:Have you tried using 3M's Micropore paper surgical tape on the bridge of your nose. I have been using the 1 inch wide tape for about three weeks now, no sore nose and it seals good too.
Dan
Hi, Dan. I used Nexcare Gentle Paper Tape early on (over a foam bandaid, before I was able to buy some moleskin). I think the thickness and cushioning of the moleskin is helpful in my situation, so I don't think a thin piece of tape would be beneficial. Plus, if my nose is somewhat tender, pulling tape off of it won't be pleasant (there was nothing "gentle" about that tape coming off my mouth in the morning when I was using the Swift LT). I have no problem with the mask sealing well, even over the moleskin, and my leak is averaging in the mid-upper 30s.
Does anyone else use tape in lieu of moleskin with success?
GumbyCT wrote:What size is your mask? Maybe you need a diff size? Has it been 30 days?
I thought that might be the case early on, grump. I was fitted with the Small cushion on 8/7. The Small cushion just clears the corners of my mouth, so I asked to try the Medium about a week later and got it on the 17th. I wore the Medium for a couple of nights, but the cushion went to the bottom of my chin, and the leaks were higher than with the Small. I suspect my "ideal" size would be somewhere between the two.
But I'm able to sleep comfortably with my mouth closed most of the time, so the Small is working out okay, size-wise. It's just the damned irritation on the nose bridge...
SaltLakeJan wrote:Hey BB,
I joined the Cpap forum about mid-January. Right after that I started exploring the different threads. You had a "Big Thread "running at that time. Through no fault of yours, you weren't getting medical cooperation or your records. I recall thinking you must be frustrated beyond description. Then SWS linked us with Mar,and we struggled through all the triplets sagas.
Remembering all the frustrations & worries we experienced, I was really thrilled when I read your comments today.
Thanks, Jan. It's been a long and winding road for me, but I'm really happy to finally be getting the kind of therapy and results that we all want, need and deserve.
SaltLakeJan wrote:BleepingBeauty wrote:I This past month with the FullLife has resulted in the best therapy I've gotten in 21 months of CPAP use. I finally feel alert again.
Congratulations R. You have worked harder than most could or would do. You kept going until you found success
Hugs from Jan
Thanks again. But I haven't done anything special. I just wanted to get good therapy, and I was willing to fight for it (which was a good thing, because I had to do just that!). I waited far too long to fire my ex-sleep doc and his Clinical Director, the charming Nurse Ratched because I trusted that these "professionals" knew their stuff. But thanks to the help, encouragement and wisdom to be found here, I became aware of how badly I'd been "treated" for all that time.
As you know, I wasn't able to "fire" that office because Nurse Ratched was reading my posts here and beat me to the punch. But she did me a big favor that day, even though I was denied the satisfaction of having my say in person. I said my piece here, and she definitely got the message.
So again, I can thank this forum for getting me to where I am today. If I hadn't found this place, I'd still be at the mercy of that incompetent doctor (who can't read plain English written on a titration report) and his ill-trained staff (who don't know how to set up an APAP for a trial).
I don't know that I'm "out of the woods" yet where my therapy is concerned. (So far, so good; but never say never.) As long as my therapy continues to be effective, I'm good to go. But if things go awry and I experience another AHI flare-up, I now have a good sleep doc who's willing to schedule an ASV titration for me.
Mar is finally making some progress with her health issues, and you will, too, Jan. We all know how much of a struggle it can be, but perseverance and a take-no-prisoners attitude helps. Hang in there, lady. I'm still pulling for you (and mar). The triplets
will be victorious! All for one and one for all!