Does Anyone Else After Taking A Shower Or A Bath Totally Out Of Air And Cannot Breath?
Does anyone else have the same problem I have whenever I take a shower or bath, I cannot breath afterwards. I cannot get to my oxygen fast enough or my albuterol machine fast enough. I am totally out of energy and air. Any suggestions or comments is greatly appreciated.
Showering does take a lot of energy. If you use O2, drape the hose over the shower curtain rod and use it in the shower. Use a shower chair so you can sit. A flexible and hand-held hose can also help. Leave the back of the curtain or door open for air and don't close the bathroom door. Have a chair waiting when you get out of the shower with a big terrycloth robe, so you can sit immediately and let the robe do most of the drying.
I answered above but here's some "extra"... I let the shower water get warm, then lean over and wash my hair. The portable oxygen unit is close by and the hose hanging from the shower door in case I fell I need it. I then wash my face and the rest of me fairly quickly and have a towel close by to do a quick dry. Then I put on the oxygen and terry robe (they're great!) and lay down for a few minutes while I dry. No problems.
Wear your oxygen in the shower. Put a showered chair in to sit on and dry off or just put on a terry robe instead of actively drying off
I'm the same way I do have a chair and wear my oxygen in the show and when I get out I put a robe on then dry off when I get more air and relax it helps some but still I hate the thought of a shower you are not alone
update for me I get in with my oxygen wash my hair rinse out sit on my chair use conditioner then soap up my body then stand up finish soaping and now i am ready to rinse everything head to toe sit and up and out then dry off and rest lotion up while sitting
Why Is It So Difficult To Shower And Get Dressed? It's My Biggest Chore Of The Day.
Oxygen & Showering + 2nd ?
I Hate Getting In The Shower Since Being Diagnosed . Does Any Body Else Have This Problem?