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Dr. Diana I am wondering if it is okay to post in this forum, and/or will you be able to answer some questions about the new POTSCare? I have read the website and received the email brochure, which are all great!
Some of my first questions: I can’t find the information for out of town patients traveling there for the week of treatment that is referred to in the FAQ’s, is that a 5 or 7 day week for testing and treatment?
Thanks so much!
Ourfullhouse, If you could be a dear and call the POTS Care office, someone can answer your questions, and I’ll still use this forum to answer more general questions. Will that be OK? It’s time for me to devote time to the patients coming in. It’s a great feeling to be able to FINALLY delve deeply into individual cases now. It’s exhausting, time consuming and takes a village, but what I love to do (geek here). I always thought we needed a group of folks looking at our cases — sort of like an episode of “House”. It only took 11 years! lol 😉
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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