Hello there @creative_writer 🙂🌺
I hope you got some rest last night 🙂
Yes - you’re right; slowly does it, and it’ll happen 🙌🏻☺️
POTS does make it really challenging to exercise…I don’t know if this helps you too, however I do most of my exercise horizontally so if I have a dramatic reduction in blood pressure or heart rate drops to 20 beats (which sometimes results in fainting if I’m upright and have been exercising), there’s less risk of dynamic shifts in blood volume away from my head.
I also wear compression socks and leggings during the day, to prevent pooling, which does help 🌺🙂
The only thing is I make sure to rest and recover fully before standing up, otherwise my eyes do go dark, but I get up slowly and incrementally so it tends to be much less of an effect 🙂
There’s lots of Pilates-like exercises that can be done while laying or side lying, which is what I tend to do, to work on core strength and joint mobility 🌺
And the loop monitor being implanted on Wednesday should give much more information regarding heart activity over the coming months, which will be helpful in deciding which treatment to do (I feel really lucky to have found an excellent professor cardiophysiologist).
im really glad the foot rollers sound like a good idea - would love to hear how they go if you do give them a try 🌺🤗
I hope your day goes well today sweetness 🥰🌺