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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: Could it be POTS?

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › POTS › Could it be POTS? › Reply To: Could it be POTS?

September 16, 2013 at 8:30 pm #4352
Napadvocate
Participant

Lab-Scientist-Lady,
I don’t think I have EDS. none of the symptoms sound familiar. I do however have a multitude of other symptoms. For example: muscle pain, joint pain, headaches sometimes migraines, sound sensitivities, texture sensitivities, trouble getting a full breath (this is a recent one as of yesterday), brain fog, excessive thirst, frequent urination, occasional stomach problems, dizziness and black outs upon standing, feet and hands tingle when I stand, extreme fatigue, insomnia, I can’t seem to stay the same temperature for very long, loss of balance/ coordination, and more that I can’t think of right now. Does any of this sound like POTS or would it just be the CFS? Also, I haven’t been able to do more than walk to the bathroom and the kitchen because of dizziness.

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