@
Gingergrrl43 if I was you I'd wait to see the ME specialist and ask him (not sure he'll have an answer).
I always bruised easily, since my early childhood and also have relatives diagnosed with EDS type III.
I was recently found to be affected by hypermobility syndrome, erroneously still called begnign by many doctors all over the world.
I'm not flexible anymore, actually the opposite, but I was as a child. True EDS experts (Dr. Francomano, Dr. Grahame, Dr. Bravo and Dr. Castori) know that many EDSrs with time and age go from flexible to stiff and the level of pain goes through the roof.
Dr. Kogelnik is aware of the connection/overlap between ME/CFS and EDS, he is also familiar with Peter Rowe's work with CFS and EDS in children/teens at Johns Hopkins.
I don't know if you want to go down the road of EDS now. I would sort out 'everything' ME/CFS related first. One can of worms at the time my dear
.
In any case there's a lot to read on and about EDS. There's a long and old thread here on PR started by @
Allyson (hope I'm correct, @
Sushi please help
.
I've always had capillary fragility, more noticeable after I had IM Infectious Mono at 14, many many years ago.
My legs look like a roadmap.
PM me if you'd like to know what is the relevant literature on EDS and overlapping features with CFS, Fibromyalgia, Dysmenorrhea etc.
In the meantime you probably can add wild blueberries to your diet.