- This topic has 1 reply, 1 voice, and was last updated 3 years, 6 months ago by .
- You must be logged in to reply to this topic.
I believe that Drs Diana Driscoll & Sharon Meglathery really should confer & pool their research to further advance their common field of EDS R&D… since they are similarly brilliant & highly motivated & personally invested by both being patients & doctors on the cutting edge of EDS research… The more they can collaborate & find more genius Zebras like them who also have EDS… the faster we all can find better treatments…
The world needs more of such collaboration on this, especially since the medical sector at large still inaccuracy assumes that EDS/JHS is rare, whereas it’s actually rarely diagnosed due to false presumptions by uninformed medical professionals…
(I’d love to become a medical research assistant myself, especially if I could make a living at it…)
I agree that Dr. Meglathery is brilliant! Did you know she wrote one of the chapters in “The Driscoll Theory”? It’s a great one — be sure to take a look! She and I are in contact fairly regularly, actually. Please know that a fair amount often takes place in the background in research. 🙂
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.
“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