HI! My dad has severe COPD and was just discharged from the hospital on home O2. He requires continuous flow at 3lpm to maintain his saturations.
He's having several night time challenges:
1. tubing gets disconnected during the night and he awakens with sats in the 80%s. Do they make alarms that would detect this breech in the system. I'm concerned the next time he won't wake up in time!
2. Any remedies besides tape to secure the cannula to his face at night?
3. suggestions for use of hearing aids with the cannula?
TIA!!!
(I am an active member of the MS Community forum here and when I couldn't find answers on google, I thought "what about HealthUnlocked?")