Dr. Diana, as Patient, explains what the symptoms of dysautonomia, POTS, Ehlers-Danlos and CCSVI feel like. You’ll hear the progression of her symptoms over the last 7 years.
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 what the symptoms of dysautonomia, POTS, Ehlers-Danlos and CCSVI feel like. You’ll hear the progression of her symptoms over the last 7 years.
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
oh my it sounded like u were describing me everything after forgeting your address! BRAINFOG
Hi Taylor,
Thank goodness it’s not just me!
Have you looked into mast cell disease, perchance?
Gentle hug,