Fundraising Page: Diane Vincent

2026 Move Your Pheet

Diane Vincent

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 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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My Badges

  • Fry Society Member
    Fry Society Member

    Awarded when Anyone reaches $250.00 in donations

    Awarded 04/12/2026

  • Most Donors
    Most Donors

    Awarded when Anyone gets the highest number of donations

    Awarded 04/12/2026

  • Fundraising Achieved
    Fundraising Achieved

    Awarded when Anyone reaches 100 % of goal

    Awarded 04/12/2026

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My Supporters

  • Diane Vincent From my favorite Conrad cousins in Massachusetts. Christy and John.  5 days ago $103.95
  • Diane Vincent This is from my good friend Laurel.  5 days ago $41.58
  • Debie Dansbe Thank you Diane for fundraising for our sweet Conrad!  2 weeks ago $100.00
  • Diane Vincent My friend Charlotte has a dear heart for Conrad.  2 weeks ago $10.39
  • Ginger Belshe 2 weeks ago $31.18
  • Diane Vincent From my favorite Conrad cousins in Massachusetts. Christy and John.  5 days ago $103.95
  • Debie Dansbe Thank you Diane for fundraising for our sweet Conrad!  2 weeks ago $100.00
  • Facebook Donor 3 weeks ago $77.02
  • Jeffrey and Kathy Marvelle 2 weeks ago $62.37
  • Lyudmila Hartt 3 weeks ago $62.37

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