Registration Details

Sign-up to walk, wheelchair roll, or help raise funds and awareness from the comfort of your couch! Registration is $10. Limited Edition POTS Walk #CurePOTS event t-shirts are $30!

How do I make the most of my personal fundraising or team page?
1. Choose a creative fundraising page or team name – have fun with it!

2. Promote your individual or team page on your social media

3. Ask others to promote it too

4. Ask families and businesses to become a sponsor

5. Have fun!

6. Send us photos showing your #STEPtember Challenge team spirit and we may feature your photos on Dysautonomia International's social media channels. Send them to: 


Please email us if you have any questions about offline donations or sponsorships, or 631-202-1720.

How do I help raise even more money for POTS research and create awareness in my community?
1. Post on social media to promote the event and show others how you are building team spirit

2. Ask your physicians to promote the event or join your team

3. Contact local media and ask them to highlight this event and/or write an article on POTS

Add a 
Limited Edition #curePOTS
event t-shirt, 
to your registration

Please note: t-shirts and prizes will be shipped to winners in the continental U.S. at no charge. If you would like a t-shirt and/or prize shipped anywhere outside of the continental US, you will be responsible for shipping fees. Final decisions on the winner from each category will be decided by Dysautonomia International.

"I'm thrilled to once again join forces with Dysautonomia International to move the needle on POTS treatment, and to someday find a cure. I'm looking forward to adding another event t-shirt to my collection!"
- Maria Finnegan, Nashua, NH

About Dysautonomia International & the POTS Research Fund


POTS is estimated to effect approximately 1-3 million Americans, mostly young women. Despite its prevalence, most people have never heard of POTS. Many doctors are unfamiliar with POTS, which makes getting a diagnosis and proper treatment extremely difficult. There is little that doctors understand about POTS and a tragic lack of funding for ongoing research.


All funds raised during the 2020 POTS Walk #STEPtember Challenge will support Dysautonomia International's POTS Research Fund, with grants going to fund the work of Early Career Investigators to promote interest in POTS by the next generation of researchers. Dysautonomia International created the POTS Research Fund in December 2013 to provide a dedicated stream of funding for POTS research. In the past five years, we have issued nearly $1.8 million in POTS research grants. Dysautonomia International is the largest non-governmental source of POTS research funding in the world.

Dysautonomia International is a 501(c)(3) non-profit that seeks to improve the lives of over 70 million individuals around the world living with disorders of the autonomic nervous system. The organization offers patient and physician education resources, community outreach, legislative advocacy and patient support for all autonomic disorders. 

Working together, we can #CurePOTS!

For more information on the 2020 POTS Walk #STEPtember Challenge, email us at:​

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