Stories

My name is Holly, I’m 26 years old. I developed PoTS in 2023, not long after having my third Covid jab, it all started out of nowhere. I was...

My name is Dillan, I am 17 years old living with PoTS. While there is no way for me to confirm it, there is no doubt in my mind that I got PoTS from...

Natasha’s Trek to Everest Base Camp for PoTS UK In November, Natasha embarked on an incredible journey to Everest Base Camp, fundraising for PoTS...

Hi, my name is Emily and I am 20 years old.  I have always been really sporty and active from a young age so being diagnosed with PoTS 5 years...

My name is Beth, I am 25 years old and have Postural Tachycardia Syndrome (PoTS), alongside living with several other serious medical conditions. My...

I’m Paul, I’m 37, based in Dorset and am an Online Personal Trainer (PT) and Nutritionist. Back in 2021 I began experiencing a number of symptoms ...

Living with PoTS means learning to take each day as it comes. It’s about listening to my body, knowing my limits, and being kind to myself. It’s...

I’m Tasmin, 30, from South West England and I was diagnosed with Postural Orthostatic Tachycardia Syndrome (PoTS) at 18. My symptoms began after a...

When people look at me, I look healthy, happy and normal (in the medical sense of the word)  but behind all of that, I’m constantly facing an...

Hi, I’m Maisie and I’ve had PoTS symptoms for as long as I can remember but wasonly diagnosed in May this year. PoTS affects me every day. Things ...