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Thank you to everyone who made POTS Walk 2021 a success! 1375 donors raised $104,000 in the month of September. These funds will support important new POTS research grants aimed at finding more effective treatments for millions of people living with POTS.
Special shout out to our team prize winners! The Fundraising Superstars prize goes to the Massachusetts POTS Walk Team, which raised over $25,000! The Team Building Rockstars prize goes to the Ohio POTS Walk Team! Great job everyone.
October is Dysautonomia Awareness Month!!! Find out how to get involved with awareness month at CureDys.org/awareness.
THREE WAYS TO GET INVOLVED
1. Register for the POTS Walk to create a personalized fundraising page. Join the state or international team you'd like to be part of when you register. If you'd like to purchase a POTS Walk shirt, you must register for the POTS Walk first.
2. If you'd rather not create a personalized fundraising page, you can donate to the state or international team of your choice, or donate through the main POTS Walk website.
3. Become a POTS Walk sponsor! Review the sponsorship packages, or contact us for assistance with sponsorships (events@dysautonomiainternational.org).
Enter the state team you would like to join in the search bar above. For international participants, enter "International Team."
LEADERBOARD
POTS WALK 2021 SPONSORSHIP PACKAGES
POTS WALK 2021 PRIZES
What is POTS?
POTS stands for postural orthostatic tachycardia syndrome, which is a disorder of the autonomic nervous system, a form of dysautonomia. The autonomic nervous system is responsible for regulating many systems in our bodies, including heart rate and blood pressure. When a POTS patient stands upright their body is unable to regulate heart rate and blood flow properly. This leads to an abnormal increase in heart rate. Because the autonomic nervous system is responsible for controlling many bodily functions, POTS can cause a whole range of other symptoms including, nausea, fatigue, sweating, lightheadedness, etc. POTS is estimated to impact between 1,000,000 and 3,000,000 Americans, and millions more around the world.
THANK YOU TO OUR SPONSORS!
A Message From The POTS Walk Chairperson
Hello! I’m Jackie Rutter Gully, Dysautonomia International Board Member, enthusiastic POTS advocate, and mom of Hanna G, a POTS patient and member of Dysautonomia International’s Patient Advisory Board who is best known for her ever-changing hair color. Our family has been involved with the POTS Walk since 2014, the year Hanna was diagnosed after spending seven years searching for the source of her seemingly myriad health problems.
The Rutter Gully family is passionate about POTS awareness, education, and, most importantly, research. Research is key to advancing the science and to finding ways to better the lives of those suffering with POTS. The POTS Walk, with its roots in Boston, has been raising funds for POTS research for six years now.
Please join us in supporting the 2021 POTS Walk, which will fund ground-breaking POTS research. Together we are WALKING TOWARDS A CURE!
Rutter Gully team members: Dylan, Jojo, Jackie, Hanna, Andrew, Jocelyn, and Tim. Supportive POTS families are the best!
Thank you for supporting the 2021 POTS Walk. Below is a summary of your transaction. An email confirmation will be automatically sent in addition to this summary.
Dysautonomia International is a 501(c)(3) non profit organization and all donations are tax deductible to the maximum extent allowed by law. Please check with your tax advisor regarding the deductibility of your contribution.
Questions? Please contact us at events@dysautonomiainternational.org
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