CPAP silicone allergy: Anyone know of other options? Solutions?
I apparently have developed an allergy to silicone, which creates problems with my cPAP mask since they all seem to be made of silicone. Anyone know of other options? Solutions? I do use a barrier (Silent Night, RemZZs) but at times they slip and I end up with skin break-down.
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Welcome @susie25, Thanks for sharing your experience. I've thought about a nose pillow mask but I'm a mouth breather and currently have a full face mask but I've thought about switching. I use a cloth cover on my ResMed AirFit F20 full face mask but I still end up with the proverbial CPAP nose 🙂. I think it's because I have to have the mask too tight for a good seal.
In the past, I've actually used those Breathe Right nasal strips on top of my nose to see if it would help but they are sometimes difficult to remove and make the nose worse. A simple kids easy to remove bandaid might be another solution. Thanks for your suggestion.
Do you mind sharing how you found Connect?
I did look at the cloth masks but with the tube connecting on the front of the face is to loud and unstable for me. My nasal pillows tube connects on top of my head and is much quieter. I did look at the other options but they did not seem like they would solve my problem.
After looking around the internet I came across this blog. I am finding it very helpful.
Thank you for your response.
I have an inhalation silicone allergy. Tried the sleepweaver anew and couldn’t get a seal. Is she a side sleeper? Whenever the mask touches anything it has a big leak? I’ve tried all sizes.
Wonder that too. I get a swollen throat, nausea and sore hands and feet from my silicone mask. Cannot find anything that works. All major manufacturers confirmed they use a mix of silicone in masks. Like you, I don’t have a contact allergy so, foam skin contact areas or liners don’t help.
Hi, it's 5 years since you wrote your post above. How are you doing?
Yes, I'm having the same problem you have. I'm allergic to silicone. The nurse in the Sleep unit told me I could try a foam mask. So, that's next. I haven't had a good night's sleep since I put on the CPAP unit before bed, 3 weeks ago. I also have a latex allergy.
I have a feeling that you and I aren't alone in our allergies and difficulties with the CPAP experience.
I'm wondering if the "cure" is worse than the "disease." The Inspire product could be next for me, and.....no, I can't imagine doing that. LOL.
It looks like I may have to go in to an informal Sleep Apnea research mode.
I did switch to the ResMed AirTouch F20 which has a foam facing melded to a silicone mask so pretty much the only thing that comes into contact with your face is the foam material. Overall I have done quite well with that option. I do occasionally experience some redness and rarely a rash on the bridge of my nose but have had no actual skin breakdown. So overall it has been a win for me (and my husband, who also now uses the AirTouch). That said, I don't know if the presence of the silicone and possible inhalation of microscopic particles from it may impact my lungs but if so, there is no really noticeable effects in that regard. I would highly recommend at least giving the AirTouch a try to see if it might work for you. (Please note: the AirTouch is not the AirFit. The AirFit has a soft silicone cushion rather than the foam cushion. My supplier has in the past mixed up the two masks once or twice, so that is something to watch for.)
I just have a slight allergy which seems to be aggravated by Revlimid.
I always got lightly pink in the mask area. Now I get hot face my nearly everyday.
I'm seriously thinking about quitting the drugs and seeing how my numbers do.
A So called Dr. First Diagnosed my nose redness as roceatia. It wasn't until years later that an allergist said I was allergic to my CPAP mask..
They all.missed the. MGUS and smoldering myeloma
Interesting on the MGUS and smoldering myeloma. I was referred to an oncologist several years ago when some of my lab work was out of whack. Further testing indicated abnormalities that could be indicative of MGUS but was not definitive. So that brings up the question as to whether there may be a correlation between the silicone/latex/other allergies and the MGUS/multiple myeloma. Just an observation and something to ponder, though probably not any real connection. Our bodies are so intricate and complicated but operate as one integrated system, so something out of order in one area can affect other areas. Despite huge leaps over the years in our understanding of the body and how it functions, we still only comprehend a small portion of the wholeness and interactivity of the created being. God's ways are indeed so much higher than we can begin to understand.
Me too. It started during the mask mandates for covid, go figure... have done everything dermatology has requested and still no improvement. Believing it is allergy to mask. I too have used SoClean machine. Everything was fine till 1+ ago.
you are NOT alone.....I too am having the same issue with no resolution
My pulmonary dr says he's never had anyone with this issue and my dermatologist has not been able to resolve. Thinking allergist is next, I know I have Latex allergy.