Hey guys!
I just had a pulseox sleep study done and it was determined that it's time for me to sleep with oxygen on at night. I've used it the last two nights and my nose/sinuses are sooooo dry and irritated. Like many of you, my nose/sinuses are AWFUL. The O2 is now drying them out which is just making every issue nose-related even worse for me. I've used a couple nasal sprays, but once the oxygen is on and blowing, it of course just dries up whatever I've sprayed (saline, flonase, etc.). Any time I've ever used oxygen in the hospital, they've hooked up a little humidifier thingy to the oxygen and that solved this problem. Do home oxygen companies offer these things for the home O2 machines? Is there something else I could use? If they do carry these things, will the doc need to write a prescription for it? I tried looking this up online, and I've only been able to find things that suggest using a room humidifier in addition to O2 therapy. That's not going to help me if it's not going up my nose, lol. Plus, I don't want to deal with a humidifier, my CF doc has always said 'no way' to using those.
Thanks!
I just had a pulseox sleep study done and it was determined that it's time for me to sleep with oxygen on at night. I've used it the last two nights and my nose/sinuses are sooooo dry and irritated. Like many of you, my nose/sinuses are AWFUL. The O2 is now drying them out which is just making every issue nose-related even worse for me. I've used a couple nasal sprays, but once the oxygen is on and blowing, it of course just dries up whatever I've sprayed (saline, flonase, etc.). Any time I've ever used oxygen in the hospital, they've hooked up a little humidifier thingy to the oxygen and that solved this problem. Do home oxygen companies offer these things for the home O2 machines? Is there something else I could use? If they do carry these things, will the doc need to write a prescription for it? I tried looking this up online, and I've only been able to find things that suggest using a room humidifier in addition to O2 therapy. That's not going to help me if it's not going up my nose, lol. Plus, I don't want to deal with a humidifier, my CF doc has always said 'no way' to using those.
Thanks!