Hii everyone,
I have pots and live in the Netherlands…I don’t feel like our medical system knows a lot about it…
I see a lot of people in the US with pots getting a liquid IV and stuff…
My doctor doesn’t want to medicate me for it since I have a low blood pressure and I don’t respond to medication well in general.
So I don’t know if there are other potsies out there in my area….that know more about this..
Hiii everyone,
I have been diagnosed with pots 2 months ago and lately I have been fainting more frequently…I think it’s the hot weather that ain’t helping…and just me overdoing it…
But I am very new to it all and it feels really scary and my boyfriend doesn’t know what to do when I faint. Does he need to wake me up?
He already lifts my legs up when I am laying down…and he always tries to wake me up…
But what can he do?
I always feel so terrible when I wake….the craziest headache and nausea…
Do you have any ideas??
Hii potsies, I was wondering for you who also use tachymon, at what heart rate do you get notified?
I have 120 and 130….but I think I need to higher it up since my heart rate can vary from 60 to 185….
I would love to hear from you…and if you don’t use tachymon (anymore) what other app do you use for your POTS….is it better than tachymon?