With an average diagnosis delay of seven years—and 80% of Australian GPs having never learned about POTS—Liv and the Dysautonomia Monsters are on a mission to change this horror story.

Please help us raise awareness, build resources, and bring visibility to the realities of living with dysautonomia.

Together, we can rewrite the ending.

I’m raising money to benefit THE AUSTRALIAN POTS FOUNDATION LTD, and any donation will help make an impact. Thanks in advance for your contribution to this cause that means so much to me.

More information about THE AUSTRALIAN POTS FOUNDATION LTD: The Australian POTS Foundation is the only national organisation dedicated to supporting, educating, and advocating for people living with Postural Orthostatic Tachycardia Syndrome (POTS) in Australia. We are entirely volunteer-run and receive no government funding. Your support helps fund Australian-led research, improve clinical education, drive health policy reform, and build a connected community for those with lived experience of POTS. Together, we can create lasting change.