RT @TheEDSociety
"If it wasn’t for The Ehlers-Danlos Society, I would still feel scared, and alone, and still wouldn’t understand why I am the way I am." https://www.ehlers-danlos.com/story/lauren-b-2/ #EhlersDanlosSyndrome #POTS #HypermobileEhlersDanlosSyndrome
#ehlersdanlossyndrome #pots #hypermobileehlersdanlossyndrome