Our Team Fundraising Page
We're raising money for National PKU Alliance!
We're participating in Move Your Pheet to raise awareness and support for the National PKU Alliance (NPKUA). PKU, or phenylketonuria, is a rare genetic condition that affects a person's ability to break down an amino acid found in protein. Without proper management, it can lead to serious health issues.
NPKUA is dedicated to funding research for better treatments, supporting families living with PKU and working toward a cure. Every step we take — and every dollar you give — brings us closer to a future without limits for those with PKU!
As you may know, our son Colter was diagnosed with PKU. We want his journey to be filled with love, support and hope. Please join us in raising money to reach our goal, or better yet, surpass it! Lets Goooo!
We all love to walk, run and bike. Our challenge to each of our friends and family is to walk, run or bike 100 miles in the month of May. And find sponsors that will donate just $1.00 for every mile you achieve! If we can have 50 members complete 100 miles and raise 100 dollars, we will meet our goal!
Please donate and help us make a difference. Your support means the world. Let’s move together and create real change!
Love,
Matt, Amanda, Wes and Colt
Recent Activity
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A donation was made to Bolt for Colt
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Daniel and Kimberly Warner donated $103.95 to Bolt for Colt
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Ali Hooten joined Bolt for Colt
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Susan Beach joined Bolt for Colt
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LAUREN WARNER joined Bolt for Colt
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Our Supporters
- Daniel and Kimberly Warner 4 weeks ago $103.95
- Susan Beach 4 weeks ago
- LAUREN WARNER 4 weeks ago $105.13
- Andrew Stanton Last month $124.74
- Jason Stanton Last month $51.97
- Linda Stanton Last month $259.87
- Andrew Stanton Last month $124.74
- Mary Diehl Last month $124.74
- LAUREN WARNER 4 weeks ago $105.13
- Daniel and Kimberly Warner 4 weeks ago $103.95
About National PKU Alliance
The National PKU Alliance (NPKUA) is a nonprofit organization dedicated to improving the lives of individuals with phenylketonuria (PKU), a rare genetic disorder. Founded in 2008, NPKUA works to advance research for new treatments and a cure, support families and individuals living with PKU and advocate for policies that ensure access to care. To learn more and get involved, visit npkua.org.
NPKUA is an independent organization and a registered 501(c)3. EIN: 26-2849140