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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.
NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › Severe, constant, chronic pain from EDS hypermobility
Are there any therapies (besides PT and prolo) that can help me? I would move wherever and do whatever to get help. My life has been completely destroyed, I had to drop out of school. I can’t work. I am only 24 and I am watching my future disappear with no hope.
Desperately searching for help and answers.
Unfortunately many people end up taking a stack of painkillers which only deplete magnesium, which makes things worse. Checkout this info on Magnesium Deficiency as a starting point:-
Dr Diana’s video on Magnesium
Hope this info will help you find effective pain management soon.
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“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