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Luckycat13

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  1. I am new to this forum but not new to dysautonomia . In 2015 I developed a myriad of over 25 weird symptoms. After much testing and specialists including autonomic testing (which was negative apparently ) the neurologist concluded that I still had some type of idiopathic autonomic neuropathy. Although this hasn't been confirmed by any medical authority I believe having a systemic mold illness in 2010 contributed to this diagnosis. I do not have pots or any other co morbidities which I am truly grateful for. I have so much empathy for those of you who have to deal with that on top of everything else. I do however have many of the other dysautonomia symptoms which I won't go into right now. Just wondering if there is anyone out there with my type of dysautonomia. Mostly everything I've researched is related to pots and rightly so because these people are really suffering . Since end of July have been in a flare possibly brought on by the heat but who knows. Never really know what my triggers are.Looking forward to any support anyone can offer.
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