Stories

I have been poorly my whole life, fast heart, fainting, nausea, etc, but no one could tell me what was wrong until… I also have Ehlers Danlos...

My name is Lisa. I’m a 34-year-old teacher and mum of two. This is my PoTS story. I had always been very keen on keeping fit. I had run 5km for...

It is difficult for me to pinpoint a period in time where I can concretely say that my PoTS symptoms started; but thinking on this now, I believe I...

Hi. My name is Joseph. I am 25 years old and I am from Cornwall and have been diagnosed with PoTS for 7 years now – it has changed my life...

I started having PoTS symptoms at 13 (PoTS was recognised even less then). I used to faint, get chest pain, have a very fast heart rate, and had...

My name is Chloe and my PoTS journey began in August 2018. I was only 16 and I had just spent the summer climbing mountains and gorges, when I was...

My name is Lois, I am 26 years old, and my PoTS Journey began in June 2019. I had always been poorly as a child, picking up any bugs which were going ...

My name is Gabby, I’m 24 and I have PoTS.I was first diagnosed with PoTS in 2018. For many years I had bouts of dizziness. At the time, I was also...

For years I’ve been suffering with high heart rate, dizziness, fatigue, headaches, brain fog, shaking, sweating and heart palpitations. No one ...

I got diagnosed at the age of 9 and I am now 15. I’m sharing my story to show the effects growing up with PoTS can have on a person in the hope ...