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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: Chest pain or costochondritis

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › Pain › Chest pain or costochondritis › Reply To: Chest pain or costochondritis

September 23, 2013 at 11:22 pm #4419
victoriafaith
Participant

Barbara,
I am a new user, diagnosed at 15, doing a PhD in Chemistry at Cambridge and sooo thankful to have found pretty-Ill! I am currently in the States recovering from a series of stem cell and other regenerative joint procedures because my experience of medicine in England is…RUN! A year and a half ago I broke my toe and requested an X-ray of my GP because I know with my EDS, things just need to be handled differently. He refused and told me to wear “supportive shoes” for the 45 minute walk to and from my lab. Several visits back to him (during one he decided to manipulate it to see if it was broken, displacing the fracture) 2 visits to A&E over two months as I progressively became unable to walk at all, the last in which I requested the MRI my American doctor said I needed and they sent me on my way saying they agreed, but had no authority to order one. I eventually had to get to London to see private Doctor who did the MRI, found 4 foot fractures, bone marrow lesions and nerve damage which required a cast for 6 months, all of which could have avoided by simply treating my broken toe! Then last November in my UK official EDS evaluation the consultant manipulated my knee for range of motion despite my plea not to…and the next day it dislocated such that I needed to go back to the states again. Lastly, 9 weeks ago both knees, back and shoulders all gave out at once and I was unable to leave my flat for 3 weeks and I felt more ill than I had ever felt in my life. My GP said it was either a virus or I was depressed. I traveled home to the states to find out the “virus or depression’ was a dural leak, and we are still trying to figure out exactly what happened to cause such a profound and sudden “disassembly”. As someone who has lived in the UK for only two years it seems that the medical system is crippled by the lack of authority to practice good medicine. Has your experience been different? Have you found any doctors who understand Classical EDS and associated issues and do you have any suggestions on how to deal with EDS and NHS?

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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

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