Joint hypermobility/EDS and ME/CFS 

This is refreshing to see on my suggested page. I have hEDS and developed ME/CFS from mono when I was 21. I felt like my hEDS became much more pronounced after I got sick, I only started dislocating things and developed PoTs after that and 7 years later I am fully disabled and still have significant crashes. I do struggle with some internalized ableism and am trying to find a way to juggle my health and being able to build my own income or find an empathetic employer. I'll save this video!

Thanks for putting this up, I have CFS and am currently seeking a hEDS diagnosis. I wished you could talk more about treatment plans

10:56 "Pesogenic papules" Thank you for this information and putting all the pieces together!

what happened to the Long Covid aspect of this seminar?