Hi guys,
Just wanted to say that our CFS/ME and Long Covid Discord server has been up and running for two weeks now and we're close to 150 members.
We're a very welcoming community that helps one another by sharing experiences, comfort and understanding.
We also have server and community events coming up soon.
If you'd like to join, the server link is below.
Chiropractics/Ostepathy for ME/CFS - worse than before!
I have Cfs/m.e and pots but am going through investigations for a 3rd time due to having vertigo etc the past 6months. Any Tips on coping? 
Canary in a Coal Mine
CFS in every day living
Hard to cope. 