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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.

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Severe, constant, chronic pain from EDS hypermobility

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › Severe, constant, chronic pain from EDS hypermobility

  • This topic has 1 reply, 1 voice, and was last updated 6 years, 1 month ago by Barbara.
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  • February 9, 2017 at 12:39 pm #1082
    sarahkooper
    Participant

    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.

    February 14, 2017 at 10:25 am #6102
    Barbara
    Participant

    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
    http://prettyill.com/videos/watch/the_magic_of_magnesium

    http://prettyill.com/forums/viewthread/1802/#5269

    http://ods.od.nih.gov/factsheets/Magnesium-HealthProfessional/

    Magnesium_and_EDS_by_Heidi_Collins_MD.pdf

    Hope this info will help you find effective pain management soon.

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