• Welcome to Phoenix Rising!

    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

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Do you take anything for POTS ?

Messages
426
Location
southeast asia
Have you been diagnosed, gone to a doctor, any test result?

There are many info about pots you can find.

Treatment usually beta blocker, electrolyte, fluid.
Things to increase blood volume.
 

bspg

Plant Queen
Messages
547
Location
USA
I don't take any medications for POTS (as mine seems to be rather sporadic) but I salt every glass of water I drink and try to drink 2-3 liters a day. This isn't a cure-all for me but it helps greatly.
 

ryan31337

Senior Member
Messages
664
Location
South East, England
Ivabradine here, 2.5mg twice daily, with a third dose on occasion if I've been busy and feel symptomatic. Works way better for me than beta-blocker.

I've also noticed quite an improvement from taking Cetirizine, 10mg twice daily. My POTS is strongly hyperadrenergic with suspicion of Mast Cell Activation playing a part, so it makes sense.

Circadin also seems to help with the sleep disruption that POTS can cause too.