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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.

Prolotherapy

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › Pain › Prolotherapy

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  • September 6, 2013 at 4:08 pm #565
    Lab-Scientist-Lady
    Participant

    Has anyone used this and had good or bad results? Does it work for persons with EDS or does it make things worse?
    Thanks,
    Shonda

    September 8, 2013 at 10:04 pm #4314
    natalia85
    Participant

    I have researched it a bit, and it is unsupported. There is not enough research to back it up, its very expensive to have done, and the reviews i got from people in my groups were 50/50.

    September 11, 2013 at 10:20 pm #4325
    Lab-Scientist-Lady
    Participant

    Thanks for the response. I am afraid there is just nothing good for us to use. Thankfully I don’t have side effects to narcotics like some people. It is the only thing I have to take the edge off the pain. I pray it stays that way. I saw my PCP yesterday and she told me to be careful that with my tissue fragility injections, surgeries, implanted devices should be reserved for last.
    Shonda

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