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!
Please donate and help us make a difference. Your support means the world. Let’s move together and create real change!
Our Team
-
Liz Colocho $110.33
-
Bruce Braughton $105.13
-
Malisa Rust Team Captain $100.00
-
Jackie Alford $53.16
-
TERESA DOROBA $32.37
-
Karina Lambertini $27.17
-
Leah Svoboda $25.99
-
Emily Holdsman $10.00
-
Lynne Messner $0.00
-
Cristian Ramirez $0.00
-
Pam Storey $0.00
-
Sommer Gaughan $0.00
-
Jennifer Coyle $0.00
-
Cherilyn Quizan $0.00
-
Frank Quintieri $0.00
-
NATALIE Beall $0.00
-
Julie Knell $0.00
-
John Doroba $0.00
-
Aurora Flores $0.00
-
Corey Robinson $0.00
-
Emily Hintze $0.00
Recent Activity
-
Lynne Messner joined PTC Therapeutics
Share: -
Emily Holdsman joined PTC Therapeutics
Share: -
Cristian Ramirez joined PTC Therapeutics
Share: -
Pam Storey joined PTC Therapeutics
Share: -
Sommer Gaughan joined PTC Therapeutics
Share: - View More Recent Activity
Our Supporters
- Emily Holdsman Last month $10.00
- Karina Lambertini Last month $27.17
- Julie Knell Last month $60.00
- Patrick Brain Phabulous cause to support! Thank you Liz! March 2026 $31.18
- Karen Koubek March 2026
- Bruce Braughton March 2026 $105.13
- Malisa Rust March 2026 $100.00
- Julie Knell Last month $60.00
- Jackie Alford March 2026 $53.16
- TERESA DOROBA March 2026 $32.37
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