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PrettyIll

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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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Viewing 3 posts - 1 through 3 (of 3 total)
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  • June 3, 2012 at 3:46 pm in reply to: Self-Diagnosis #2328
    Only You
    Participant

    You seem to enjoy learning Maffin!

    Maybe these will help
    http://www.pspinformation.com/disease/otherdiseases/hypotension.shtml
    http://www.cybermedicine2000.com/pharmacology2000/Autonomics/Adrenergics1/Adrenergic-53.htm
    http://nursingpharmacology.info/Autonomics/Adrenergics/Adren1.htm

    June 2, 2012 at 3:50 am in reply to: Self-Diagnosis #2311
    Only You
    Participant

    Holy shit. I was not expecting that response. You obviously take your health seriously.

    If there’s anything to say it’s thank you for such a real description.

    June 1, 2012 at 10:26 pm in reply to: Self-Diagnosis #2303
    Only You
    Participant

    Finally, someone with EDS who takes modafinil! I read it’s used off-label for CFS so I was thinking of trying to get it from my doctor. what does it do for you? And are the other drugs worth looking into as well?

    I’m sorry I don’t have anything to add about POTS. I’ll look around for you though!

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Viewing 3 posts - 1 through 3 (of 3 total)

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This website was created to inform, educate and brainstorm with fellow patients and doctors. The content should not be used as a substitute for professional medical advice, diagnosis or treatment. Readers are encouraged to confirm all information with other sources and their physicians. The creator of this site will not be liable for any direct, indirect, consequential, special, exemplary, or other damages arising from the use of this website.

Twitter: @prettyill

What others say

“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

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