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tigger2512

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  1. it says no attachment available.
  2. I carry the bp machine and pulse ox in my handbag now!
  3. Hi, Yes they did mention the salt intake and drinking more water. I have tried that and now trying the increase of the toporol xl to 25 mg. I was just never "truly" diagnosed with it and it came literally from nowhere. 3 years ago i was at my neighbors having coffee and everything went fuzzy and said i'm going to pass out...it was the worst feeling ever and i had never had it before and it hasn't stopped since...not all the time but i just never know when and i'm afraid to drive far alone or even go to a store myself.
  4. Thank you, The EP doc had mentioned the tilt table test but nothing was happening with covid. I'll see if the toporol helps for now. Lucky for me I have a local Walmart because i don't go very far the last 3 years since this started.
  5. I actually can't believe i found this site. I have been having these "episodes" for 3 yrs now..i have seen every doc in every specialty and no one has an answer for me...i have had numerous stress tests and heart monitors. I never had the "feeling of fainting" while wearing the monitor up until the last one..i had the fainting feeling 3 times and the heart monitor showed absolutely NOTHING. I actually was sitting in the aisle of a supermarket it was so bad. I get a very strange feeling sometimes...i feel "funny"..light headed NOT dizzy. I feel like the lights get dim and i'm not there. There isn't any thing that causes this and i can go weeks and sometimes months without it happening and then it just does. I'm afraid to go anywhere myself and my life has been h*** the last 3 years. It started out of nowhere. The cardiologist put me on toprol xl 12.5 once a day and that's not helping so yesterday he raised it to 25 mg a day. I do NOT have high blood pressure. I just don't know where to go or what to do at this point. I made another neurologist appt for July because the last time i went to one they threw back to the cardiologist. I have no idea what is happening to me and everything i google (pretty sad that's how i have to get my own diagnosis) points to this and pots.
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