| Joined: Aug 2010 Posts: 8 Member | OP Member Joined: Aug 2010 Posts: 8 | I have moderate sleep apnea and use a CPAP with humidifier, and nasal pillows. That worked fine through most of treatment, but the last couple of weeks, when the dry mouth and the burns in the mouth got really bad, the CPAP made me miserable. The nasal pillows (instead of a nose mask) put extra airflow through the nose, and were VERY drying to the back of the mouth and throat.
So I just wasn't sleeping. Finally realized a couple of things, and got real sleep last night without so much discomfort. Thought I'd post here in case anyone else has similar experiences or something to add.
1. I switched from nasal pillows to a mask,and that really helped with the dryness. 2. I'd been using the built-in humidifier on my Respironics System One. It's never been impressive, since even at maximum it doesn't seem to use more than 1/8 cup of water per night. Since I live in a desert area, that doesn't raise the humidity enough. I remembered I have an old Fischer Paykel HC100 humidifier which is more robust. On its highest setting I thing kit can use 1 cup of water per night. Switched over to that, and got some relief.
Anyone else have suggestions/experience with CPAP's when the mouth sores and burning are bad? How about after treatment...just ongoing with the dry mouth so many of us have?
SCC of buccal mucosa T1N0M0. DX 7/10. Surgery to remove on 8/10 successfully removed the growth. IMRT ending 11/10
| | | | Joined: Sep 2010 Posts: 8 Member | Member Joined: Sep 2010 Posts: 8 | My husband also has sleep apnea and used a CPAP regularly for years. He was not able to continue with the CPAP during treatment. We are 3 months post treatment, and he still cannot use it yet due to the dryness and mouth pain that results. So, he sleeps propped at an angle. Hopefully things will get better over time.
Kevin
Age 42, Stage 4 SCC w/Right Tonsil and 6 nodes positive, Neck Dissection 6/01, 35 rads with 1x/3wk cisplatin, peg 7/2010. completed treatment 8/17/10.
| | | | Joined: Sep 2006 Posts: 8,311 Senior Patient Advocate Patient Advocate (old timer, 2000 posts) | Senior Patient Advocate Patient Advocate (old timer, 2000 posts) Joined: Sep 2006 Posts: 8,311 | Even though my dry mouth improved gradually after my treatment ended I didn't see a great improvement in my dry mouth until 15 months post Tx.
David
Age 58 at Dx, HPV16+ SCC, Stage IV BOT+2 nodes, non smoker, casual drinker, exercise nut, Cisplatin x 3 & concurrent IMRT x 35,(70 Gy), no surgery, no Peg, Tx at Moffitt over Aug 06. Jun 07, back to riding my bike 100 miles a wk. Now doing 12 Spin classes and 60 outdoor miles per wk. Nov 13 completed Hilly Century ride for Cancer, 104 miles, 1st Place in my age group. Apr 2014 & 15, Spun for 9 straight hrs to raise $$ for YMCA's Livestrong Program. Certified Spin Instructor Jun 2014.
| | | | Joined: Aug 2010 Posts: 8 Member | OP Member Joined: Aug 2010 Posts: 8 | 15 months, yikes. My dry mouth is still getting worse. But the CPAP is at least tolerable now that the burns in the mouth are healing and I've been able to pump up the humidity.
SCC of buccal mucosa T1N0M0. DX 7/10. Surgery to remove on 8/10 successfully removed the growth. IMRT ending 11/10
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