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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: New Here – History Of Mvp, Syncope, Pots, Possible Mast Cell

NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › POTS › New Here – History Of Mvp, Syncope, Pots, Possible Mast Cell › Reply To: New Here – History Of Mvp, Syncope, Pots, Possible Mast Cell

June 17, 2012 at 8:46 pm #2444
ScaredSingleMamainMaryland
Participant

Hi Tristessa! I just started here recently. These symptoms sound a lot like mine. I have officially been diagnosed with allergies, anaphylaxis, SVT, asthma, GERD, IBS, AUB, Fibromyalgia, migraines, partial seizures, neuropathy and POTS over the years. I began having some symptoms (mostly bone pain and horrible fatigue) as a teenager, then I began w/anaphylaxis after my daughter was born, in 2009 my cardiac symptoms began (ran in cycles), and then as of February of this year everything just started going downhill real fast. Right now I am house confined other than grocery shopping and doctors. It is horrible living like this (though of course I am grateful to be alive) but worse real recently my nearly 9 year old daughter has began with POTS like symptoms : * ( At any rate, it is nice to “meet” you I am ye and I will keep you in my prayers. I hope things get better for you. I am here if you want to talk.

Ang.

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