Fundraising Page: Cheryl Connor Team Page: Team Evan Almighty

2026 Move Your Pheet   ○   Team Evan Almighty

Cheryl Connor

March 18, 2026 12:00am - May 31, 2026 11:59pm

My Personal Fundraising Page

I'm raising money for National PKU Alliance!

I’m participating in Move Your Pheet in honor of our grandson, Evan 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 I take — and every dollar you give — brings us closer to a future without limits for those with PKU!

Please donate and help make a difference. Your support means the world. Let’s move together and create real change!

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Join My Team!

My Badges

  • Fry Society Member
    Fry Society Member

    Awarded when Anyone reaches $250.00 in donations

    Awarded 04/22/2026

  • Team Fundraising Leader
    Team Fundraising Leader

    Awarded when a Team Member raises the most funds for their team

    Awarded 04/22/2026

  • Fundraising Achieved
    Fundraising Achieved

    Awarded when Anyone reaches 100 % of goal

    Awarded 04/30/2026

  • Top Fundraiser
    Top Fundraiser

    Awarded when Anyone raises the most funds

    Awarded 04/30/2026

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My Supporters

  • Kelly Connor 14 hours ago $1,039.50
  • Marian Hogan 1 week ago $25.99
  • Colleen Rigley 2 weeks ago $30.00
  • Bill & Nancy Wladyka We love you Evan! 2 weeks ago $103.95
  • Bill Wladyka Last month $51.97
  • Kelly Connor 14 hours ago $1,039.50
  • Bill & Nancy Wladyka We love you Evan! 2 weeks ago $103.95
  • Cheryl Connor Last month $55.53
  • Bill Wladyka Last month $51.97
  • Facebook Donor Last month $51.52

My Teammates

My Activity

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