This October, Grace and I will be walking 150km to raise money for POTS (postural orthostatic tachycardia) and Dysautonomia!

I was diagnosed with POTS and hyper-mobility in 2023 after a long 2 years of no answers. Many doctors had/have never heard of POTS and this needs to change.

POTS affects a persons everyday life as it is a complex condition where the autonomic nervous system doesn't properly regulate body functions causing an excessive heart rate increase, which then leads to heaps of other symptoms.

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.