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.
I live in Memphis,TN. My daughter and I were diagnosed by a genetisit at Vanderbilt three years ago. Most doctors here arent familiar with EDS or know enough that they dont want to see you! Still havent found a rhuemy for myself. Wondering if we should just make the trip to Baltimore for both of us and get as much info as I can! My four year old has a good cardiologist that deals with EDS. Her rhuemy is pretty amazing as well. I have had much better luck with the pediatric side than adult and even that is minimal. How do they test for POTS?
I have EDS hypermobility and have this pain. I just thought it was related to being tired & stressed. What type of doctor do you see to get a diagnosis for any of this?
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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