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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: Did you see the ISNVD press interview?

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › Did you see the ISNVD press interview? › Reply To: Did you see the ISNVD press interview?

March 9, 2012 at 7:03 pm #1815
Dr. Diana
Keymaster

Hi,

I’m Jendays247 from YouTube. 🙂 Thanks for the Big, BIG hug the other day when I was watching your speech crying!

I did watch the press interview, and it answered A LOT of questions for me. I actually found a couple of doctors right near where I live (one is only about 5 minutes away). Of course, there was some controversy about whether or not the doctors are still researching CCSVI or dx/treating it (the posts I found were not very recent).

Thank you for all you’ve done. Really. You have taken so many of us who feel like pieces of a puzzle that just do not fit, and you’ve created an entirely new picture of which we can be a contributing, appropriate, and accepted part.

I have to do something, and soon. I’m just getting sicker (but I look good!) and more fearful with each passing day.

Jen

Jendays247!! You’re here!! I’m so happy!! My friend, we are getting some answers, and I humbly believe we are getting to the bottom of this! I don’t think it will be hard to prove what is wrong with us, and I’m working on “fixes” until they can change our genes. There is so much hope for us right now. I’m not very good about waiting around, so I’ll be up front and center with more info soon. No need to fear (Underdog is here. sorry, couldn’t resist that one. I love Underdog). Please stay close by — I’ll be announcing a registry of sorts soon that you can participate in from the relative comfort of your doctor’s office! How does that sound? Again, I’m so glad you are here, and I’m never short on hugs. Here’s another one. ((((hug)))) 🙂 Diana

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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.”

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