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.
Sorry to hear about what’s going on. My story sounds similar to yours. I was just diagnosed with cci in December. I also have chronic lyme but can’t afford treatment right now. The pressure in my head is what’s driving me nuts. I’m mostly homebound because of the head pain.
Do you find your headaches to be worse when upright? Do you have a bobblehead feeling? Have you ever had a spinal tap done?
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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