What if you went to get up one day, but couldn't?
People suffering from POTS miss out on so much of life and then become the missing. Help us sponsor research into POTS and provide advocacy so people living with POTS can get the treatment and support they need.
Our Mission
A brighter future for those living with POTS, through advocacy, support and research.
The Australian POTS Foundation is committed to improving outcomes for those with POTS by raising funds for improved research, advocacy and support for those living with POTS. The Foundation is currently run entirely by volunteers. Beyond minimal running costs, all funds raised will go directly to improving research, education and support for those with POTS in Australia.
What Is POTS?
Postural Orthostatic Tachycardia Syndrome, commonly referred to as POTS, is a complex and often misunderstood condition that affects the autonomic nervous system. This system controls things your body does automatically such as controlling your heart rate, breathing and digestion. When it’s not working correctly, it can cause a multitude of symptoms that seem unrelated to each other.
Sometimes POTS is referred to as dysautonomia, which is an umbrella term for multiple conditions that affect the autonomic nervous system.
The Australian POTS Foundation is a proud member of the Australian Patient Advocacy Alliance.
To find out more:
Go Fund Me - 30 BPM
Here's How You Can Get Involved
Advocate
Spread The Word And Help Raise Awareness
Donate
Contribute Financially To Help People Living With POTS
Volunteer
Make A Difference By Volunteering with the Australian POTS Foundation
Become a Member
Join Us In Championing The Needs Of The Australian POTS Community
Use Your Email Signature
Every time you send an email, if you have one of our email signatures in use, your recipients will learn something about POTS and your experience of living with POTS.
We have created some text and images that you can copy and paste into your email signature settings in most email software or systems.