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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: Forum problem

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › Forum problem › Reply To: Forum problem

September 8, 2011 at 11:34 am #1463
Petroglyph Caroline
Participant

Hi Everyone,

My name is Caroline, and I’m the designer and developer of this website. I wanted to address some of your concerns.

Firstly, I’m sincerely moved by the coming together of this community. I’m so pleased that these forums and this site are so meaningful to you.

Also, I wanted to apologize for your hard-worked posts and replies being thrown out as spam. We’re doing everything we can to make this forum useable for everyone, while keeping it clean of unsavory spam and abuse. That said, we are using a few out-of-the-box solutions and (unfortunately) discovering some system limitations to the software in place.

While I understand that this is frustrating to anyone, I’d like to thank you in advance for your continued patience as we continue to do our best to work these kinks out. We’re doing our best, as anyone would, to make this a great place for learning, connecting, and sharing.

Meanwhile, I look forward to hearing any comments or suggestions.

Many thanks,
Caroline B.

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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.

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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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