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.
CFS in every day living
CFS Clinics, Gluten, Thyroid
This edema of my body is really upsetting and gross.
Call out for ME/immunologist private specialists 
Feel worse in mornings?