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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: confused about dysautonomia

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › confused about dysautonomia › Reply To: confused about dysautonomia

October 17, 2013 at 11:57 am #4520
Soprano1
Participant

Thank you so much for the info!! Wow, I most definitely have dysautonomia!! It seems that Chiari symotoms are there as well but are little less pronounced than the dysautonomia symptoms. And I just googled livedo reticularis and that definitely seems to look exactly like what is going on with me arms. I’m not sure if I have ever been tested for an Antiphospholipid problem because my doctors seem to just run a boatload of blood tests on me and they never tell me what they were testing for!! Like Dr. Diana recommends, I have to start asking for the raw data so that at very least I can find out what the heck I have even been tested for.

I do have a positive ANA and a speckled pattern immune system though….

Thank you again for the great resources! 🙂

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