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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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Janelle

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Viewing 2 posts - 1 through 2 (of 2 total)
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  • September 24, 2013 at 4:51 pm in reply to: chiari malformation? #4421
    Janelle
    Participant

    I am beyond frustrated at this point. My MRI results game back normal of my brain… I have EDS and POTS and autonomic dysfunction and I have most all the symptoms from chiari I thought for sure they would find something. My entire head base of skull hurts and when I press on it, it feels like a bruise and feels like releasing pressure, I have had swallowing issues throat soreness, hoarse voice different times throughout the day and major headaches that radiate from the back to my ears and behind my eyes. Does anyone else see anything wrong with this MRI? I am not convinced this is normal and will be sending my records for a second opinion. Thanks

    September 22, 2013 at 12:18 pm in reply to: chiari malformation? #4414
    Janelle
    Participant

    Thank you, Thank you and Thank you!! I am so nervous about my appointment and having some understanding of what I am looking at and feeling makes so much more sense now which gives me relief in that area. I will keep you posted

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PrettyIll.com

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

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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

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