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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: I am so lost in this forum.

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › POTS › I am so lost in this forum. › Reply To: I am so lost in this forum.

March 24, 2013 at 12:28 am #3559
capri
Participant

I can’t figure out how to post or respond where I want to… (this is a dart in the dark.)

Any navigtion suggestions/advice for a newbie?

Hi Capri, Welcome!! New forums can be so weird at first, but we’ll try to talk you through it, OK? You did great posting a question! To respond to a question, just click “post reply” — this button is on the upper right, or “quote” — down below (if you want to quote the original author first, as I did on this one). The main list of topics should pop up on the first page — just scroll down. Pick a general topic, and then post your question. Does this help? Big hug, Diana

Yes, and Thank you Dr. Diane… I’m learning my way around a little better… I was first concerned about posting under the correct topic area, but I’ve since found where they are listed… Hopefully I’ll remember to post my questions under the category where they are best suited. If I mess up.. plz forgive a newbie. Best to all.

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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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