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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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Badges etc

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › Badges etc

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  • October 16, 2012 at 12:03 pm #336
    stryderslist2
    Participant

    I wasn’t sure where to post this (again) but I have uploaded a few badges that you can use on your facebook pages, avatars, etc here: https://www.facebook.com/media/set/?set=a.506725019340538.120937.500570473289326&type=1

    I will be adding these to the store and 100% of the profits will go to Dr. Diana and her research. I hope we can all work together and help her achieve some great results. I know she has helped me and my son so much and I can’t thank her enough.

    I will be adding other buttons, colors, etc, so if you have any requests, please let me know either on the FB page or email me at anj@stryderslist.com

    The store address is: http://www.cafepress.com/stryderslist

    Please also go like the Facebook page so you get notified when a new tag is loaded.
    https://www.facebook.com/pages/Invisible-Illness/500570473289326

    You will need to copy and paste the links for them to work

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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

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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