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.
Also, let me add that I have POTS and didn’t know there was such thing as Hyperagenergic but always wondered why my blood pressure would rise instead of fall & such. I had my doctor run the 24 hour testing and blood work for that and most of it came back elevated. I don’t seem him until next Friday but am wondering if that means I have Hyperagenergic POTS then?
Thank you both for the responses. This makes me feel better! I am back on a low dose of propranolol and feel like I’m no longer dying. 🙂
Dr Dianna,
Thank you for getting back to me on this topic. I have decided to continue with depo as I know it stops my periods and my horrific dysautonomia symptoms at that time of the month. I am seeing a specialist in May and am going to get his opinion also. I will keep you updated, and would love to here from anyone else with experience with this.
Thanks,
Ashton
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.
Twitter: @prettyill
“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