Invisible Illness
This is a great video (although not about EDS specifically) that demonstrates how people with an invisible illness--EDS, Dysautonomia, Fibromyalgia, Lupus, ME--would like to be treated just like everyone else. Just because you can't see the illness or disorder, does not mean that it doesn't exist.
My name is Jill and I am 29 years old. I am a former competitive gymnast and I have Ehlers Danlos Syndrome (hEDS), Chiari Malformation- Type 1 (8.5mm herniation), craniocervical instability, Neurocardiogenic Syncope and POTS (forms of Dysautonomia and secondary conditions to EDS), slight/minor Mitral Valve Prolapse, bilateral acetabular hip dysplasia (corrected in a procedure called Periacetabular Osteotomy--PAO), gastroparesis and delayed intestinal motility, Hashimoto's, Graves', Autoimmune Neutropenia, and Complex Regional Pain Syndrome (CRPS).
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