I feel exactly the same and have had so much treatment for anxiety and depression but because they don’t know how to treat my POTS and EDS. They keep coming back. It’s so draining telling people I am anxious about everything, including going to the cardiologist to go over the same symptoms, for me to then feel like they are not listening when I say how utterly exhausted I am or how my migraines make me want to pull my head off not to mention my other symptoms. I hate that you feel the anxiety too but I hope you can take some comfort in not being alone in feeling this way.
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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