Hey all. Today my partner (Danielle) was diagnosed with pots syndrome and we was told about a wonderful site we could visit for support for her. So here we are giving you all a wave from us ππ»ππ»
Pots syndrome : Hey all. Today my... - Unexplained Faint...
Pots syndrome

Written by

Aston_Danielle2014
To view profiles and participate in discussions please or .
5 Replies
β’
Hi . Have you looked at potsuk.org/
It's a really informative website with great information. It really helped me when I was diagnosed. I hope all goes well for you.
I printed the info for doctors page off for my GP as little is known about it by most doctors. The lifestyle changes can really help. It took a lot of trying different types and sizes but the compression socks and increasing salt and water intake really helped.
Not what you're looking for?
You may also like...
Do I have POTS syndrome?
Hi, I would welcome your opinion I'm new here.
I'm 51 now (male)and my symptoms started after a...
Pots digestion issues
Hi I am newly diagnosed with pots and my sever bloating when ever eating food is getting really...
Deperate newly diagnosed pots sufferer
Good evening I am new to the group recently diagnosed with pots after a 2 year battle. I have...
Sudden slow pulse with POTS?
I am still in the process of waiting for tests but have unofficially been diagnosed with POTS. I...
Pots diagnosis after 25years of symptoms. Does CBT help?
I'm 39 and was diagnosed with pots following tilt table test after a GP finally connected the...