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.
Thank you Jewels! I think about the only “exercise” I can tolerate is in the water. My joints are way too loose for anything else. Thanks so much for responding, sounds like I’m in the right place! 😉
Ok, so I am getting a little nervous that 18 people have read my symptoms and have not responded. I watched the videos but am am not as familiar with some of the terms/abbreviations so I posted my symptoms in hopes someone could tell me what kind of Dr I need to see. My Rheummy doesn’t know how to treat me, my cardiologist has never heard of it, my orthopedic surgeon is afraid to do surgery on me, I’m his first EDS patient. Am I in the right place? I see a geneticist in October, does he treat all of these sumptoms? No one has ever talked to me about EDS. I’m on my own… Well except I have the Lord and a really awesome husband. 😉
This website was created to inform, educate and brainstorm with fellow patients and doctors. The content should not be used as a substitute for professional medical advice, diagnosis or treatment. Readers are encouraged to confirm all information with other sources and their physicians. The creator of this site will not be liable for any direct, indirect, consequential, special, exemplary, or other damages arising from the use of this website.
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