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PrettyIll

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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: Newbie looking for advice about symptoms and appointments

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › Newbie looking for advice about symptoms and appointments › Reply To: Newbie looking for advice about symptoms and appointments

August 25, 2013 at 7:17 pm #4216
Lab-Scientist-Lady
Participant

Jen,
About you little brother. He sounds a lot like me. Pain is a hard thing to live with, and I think a lot of people with EDS think about suicide or carry through with it. I wonder how many cases are persons with EDS that never knew they had it? When I went back through my family history I found two persons that were thought to have killed themselves. Alcoholism was prevalent too. Looking at their pictures they had the EDS look. I hope your brother will get help. Maybe he should move closer to you? Y’all could be your own support system.

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