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.
Oh wow! Someone else like me. I’m so excited I don’t know what to write first. I have had this half red, no sweating face for a year now. I noticed your pupils are wide open, even though it seems to be bright in the room. Do you have tonic pupils? I have tonic pupils. They are very slow to react to light changes. I walk in from the bright sunlight into a darker room and all I can see is a greyness. Holmes Adie is what they told me it is. Some of my eye pals have Ross syndrome. They compensate and over sweat on one side of their face because the other non red side is not sweating. But I think I’m having mast cell issues. I have multiple IgE mediated allergies. All cow, soya, grass, trees, latex, drugs. From what I’m reading though it is hard to get a diagnosis of Mast Cell problem here in the UK. This is a link to a picture of my half red face.
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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