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
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.
I feel for you Mama. I have three little guys 6 & under and all three are on the spectrum as well. I really have thought long and hard about my oldest son having POTS symptoms as well. It is sometimes hard to tell what is ‘spectrumy’, typical or ‘potsy’. I will keep you in my prayers as well. Have you considered mast cell activation issues at all? I am really wondering if this might be the missing link for us. My sons (and me) have varying degrees of food allergies and intolerances. My oldest has anaphylaxis to dairy (milk) and any nuts. His reaction can be triggered by skin contact or even inhaled fumes. It is crazy, crazy!