#pots uk

[joes-sha-la-la-la-girl]

If it ain’t the hypermobility then it’s the PoTS and if it ain’t either of them it’s the scoliosis. One day is all I ask 😫😭

[coto524]

Starting TOMORROW, two of my mates are doing a 24-hour stream to raise money for POTS UK!

Jonas and Jamie are lovely guys, friendly and hilariously funny, and their podcast The Bunyip Review is one of the highlights of my month! They first agreed to do a 24-hour podcast three years ago — this has been a long time in the making but will doubtless be worth the wait 💜

The stream starts at 15:00 BST (that's 10:00 Eastern / 07:00 Pacific) on Saturday 1 July — come along and join the fun! All funds raised are going to POTS UK, a charity which promotes awareness and support for postural tachycardia syndrome.

Donations open now! bit.ly/24hourpod

Watch on Twitch: twitch.tv/thebunyipman

[joes-sha-la-la-la-girl]

So as most of you know now I was diagnosed with PoTS on 2nd October of this year. It’s only been 3 weeks since the diagnosis but I’ve been living with the symptoms for months now. Here’s some information from PoTS UK with more information 💖

https://www.potsuk.org/about-pots/what-is-pots/

[kitt66]

Postural Tachycardia Syndrome (PoTS) is an illness that especially affects young people. They often find the symptoms, including dizziness, anxiety, stomach problems and passing out, mis-diagnosed as being simply consequences of their age. The more that people know about this syndrome the better, so I wholeheartedly support the work of the charity POTS UK, which aims to increase awareness of the syndrome amongst both the public and health professionals. I hope anyone who recognises these symptoms will check out the website and realise that help is at hand and that they are not on their own.

Peter adding his support to POTS UK