Dr. Diana as patient discusses chronic fatigue, Ehlers-Danlos (EDS), CCSVI, POTS, fibromyalgia, dysautonomia; She answers some questions and introduces her story.
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 discusses chronic fatigue, Ehlers-Danlos (EDS), CCSVI, POTS, fibromyalgia, dysautonomia; She answers some questions and introduces her story.
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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, my name is Jamie I am 32yrs old and I have been diagnoised with EDS. My Dr. thinks I possibly have MS. I als have symptoms of POTS. On my fathers side of the family there are10 siblings and 2 of them have MS and 3 of them have Fibromyalgia. It has taken me many yrs to get the diagnoisis of EDS. But I have been left to do the research myself. I realize that I am getting more anxiety from the Dr.’s not having the time to educate me or take my health serious. I would love to… Read more »
Hiya dr diana, I am looking for a bit of advice. Im natalie aged 22 and live in Scotland, UK. I have been diagnosed with eds 7a/b. I dont have a consultant as there isnt one in Scotland and my old consultant Professor Bird who was in Leeds, England has retired. My eds has got a lot worse in the past 18 months and I am now in a wheelchair, can walk a few steps but any more than that I am dislocating my lower joint. I have also been suffering from seizures, upto 30 a day. I have had… Read more »