A very educational post about a ME/CFS /Long Covid experience from the perspective of a person with an occupational/physical therapy background.
A very educational post about a ME/CFS /Long Covid experience from the perspective of a person with an occupational/physical therapy background.
I’ve tried physical therapy several times - and unsurprisingly to anyone who understands PEM, as I gained muscle strength, my endurance got worse and I slowly crashed.
My dream one day is to be able to create my own physical therapy plan. I have some ideas that revolve around some guidelines I’ve found about aerobic respiration dysfunction, mainly:
But unfortunately my health isn’t there yet. A lot of this is based on this overview of CFS/ME for physical therapists, and this part struck me:
I don’t really consider myself to have trouble with ADLs (Activities of Daily Living), since they’re so limited. I can basically shower, dress, and eat on my own, with appropriate aids. (I mean sometimes I skip showering and sometimes I need help putting on compression socks but it’s not bad.)
But I hadn’t heard of IADLs before.
The only one of those I can do regularly is finances, so… Yeah. Not ready for DIY PT…
That sounds like a cool PT plan. I wish you that you will be able to start it someday. And hopefully you will be able to get some healing.