What’s the theory behind the connection between Ehlers-Danlos Syndrome (EDS) and ME/CFS? (Other than CCI/AAI)

I now suspect I had EDS all my life without knowing. I will get tested for it in a couple of weeks. I will also get an MRI of my brain and neck.

I got sick from covid in april and I’m trying to understand the connection between EDS and ME/CFS. I have POTS now and I know about the connection between POTS and EDS (and MCAS). I have also read about CCI and other spine and brain conditions. But I can’t find much research or other information about EDS and ME/CFS.

I don’t think all who have...

What’s the theory behind the connection between Ehlers-Danlos Syndrome (EDS) and ME/CFS? (Other than CCI/AAI)