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Everything posted by shasta43

  1. hey all. i am scared. ill be straight up. im newly dx with pots and i have antibodies associated with both sjogrens and lupus. does anyone else have a possible autimmune cause for their pots? i saw a cardio who dx my pots and then said ill see you in a year...i was disappointed. also about the cause of this disease.. there has to be a reason for this syndrome? a causative agent? you body doesnt just go haywire for no reason does it? last thing... do any of you feel dizzy even while laying down at times ? sometimes i get a falling sensation like i am falling through the floor. i hate it. I
  2. i was recently put on miranol which is a synthetic canabanoid for pots from my dr at johns hopkins for its supposed ability to calm and relax pots patients being that one of my complaints and many complaints of pots patients is the physical anxiety that comes along with this dysautonomia condition. I took one pill. one stinking pill at 2.5mg and within an hour i couldnt speak and whole body was completely numb. pulse was 150 sitting and I was having palpitations and could not move my arms. my wife called 911 and i was rushed to the ER feeling super weird and like i was going to die. it made
  3. Hey yall im new to the site but I am currently being followed by a rheum at johns hopkins and lab work recently was positive for ANA and ANTI SSA which rheum said is sometimes seen in patients with lupus and or sjorgens. I began having dysautonomia/pots symptoms about 6 months ago and have dry eyes. although i do not have a formal diagnosis of sjorgens or lupus it makes sense that sjorgens could be causing autonomic dysfunction in me due to nerve damage. I have tachycardia with standing but also sensitivity to light and noise. I hope my rheum can connect the dots and start me on some medicatio
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