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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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Reply To: Newbie feeling very lost

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › Newbie feeling very lost › Reply To: Newbie feeling very lost

September 5, 2013 at 1:55 pm #4286
Lab-Scientist-Lady
Participant

Looks like I cut of part of Dr. Diana’s list. Here is the rest:

Interstitial cystitis (feels like you often almost have a UTI) or pelvic pain syndrome
Do you have other autoimmune conditions such as Rheumatoid Arthritis, M.S., Sjogren’s, etc?
Is there a family history of mental illness?
Is there a family history of Alzheimer’s Disease?
Are there autoimmune conditions in your family?

By completion of this poll, I hereby certify that I am an individual with a suspected or confirmed
diagnosis of dysautonomia and or M.E./ Chronic Fatigue Syndrome.

I understand that my identity will be held strictly confidential, and only used only to confirm the ethics of the poll.

If you do not wish to participate in further studies (likely based on your results), please indicate here:

Thank you so much for your help in getting out the word to the world that we suffer with more than fatigue!

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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

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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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