EDS & Why We Misunderstand Disability
I find this video incredibly relatable. I’ve not been formally diagnosed with any version of EDS but I definitely have some sort of hypermobility disorder, and it’s definitely related to my fibromyalgia diagnosis. Everything she shares in her story is super relatable. Including the specific experiences with physiotherapists and being doubted by every doctor, and everyone blaming me being “out of shape” or having a “weak core.”