Dr. Diana as Patient explains the various forms of Ehlers-Danlos Syndrome (EDS)
Dr. Diana, both a doctor (therapeutic optometrist), and a recovered POTS and ME/CFS patient, offers help and hope for POTS, Dysautonomia, Ehlers-Danlos syndrome, Chronic Fatigue, Chronic Lyme, vascular abnormalities, Fibromyalgia, and Multiple Sclerosis. Dr. Diana is now working full time at POTS Care.
Dr. Diana as Patient explains the various forms of Ehlers-Danlos Syndrome (EDS)
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Twitter: @prettyill
“Dr. Diana will always hold a very special place in my heart for her selfless devotion to helping everyone, not just the Ehlers-Danlos community. I hate to think what my life would be without her insight and guidance.”
-- Chris Gross
Hi, I’m trying to wrap my brain around all this stuff. I’m not formally dx with EDS hypermobile (don’t appear to be *any* knowledgable docs even within 4 hours 1-way drive), but have what I’ve been thinking is a “mild” version of it, but enough that by now I am disabled for work purposes, and I also have a number of associated things like blue-gray sclera, gastroparesis (again “mild”) with reflux (“mild”), and other stuff (but not POTS but maybe some “mild” dysautotomia) … I was surprised to hear you say that EDS pretty much requires a lot of pain… Read more »