How did they diagnose that? I’d love it if someone could find anything tangible with my LC.
Hi. Have you seen this info? https://covid19criticalcare.com/protocol/i-recover-long-covid-treatment/
It’s too much for me to read entirely. But generally doctors are just throwing shit at the condition and try to see what sticks. There is still much research to be done to see what really helps besides aggressive rest.
Hi, i’m wondering since you’re moderating CFS and Encephalomyelitis, and here you’re talking about LC, if i can read your story somewhere
I don’t have anything concentrated. There might have been a post on my blog at https://bjoern-tantau.de but that’s probably in German.
i’m glad i can read some german. Quite some misery you’re going through :( regarding the link i gave; i guess you saw it. i wonder what your take on it is. cheers
