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Our ambition is bold:
to change the lives of children living with PPP3CA and beyond.
Partners in research and builders of a global community - bringing hope, answers, and a path to treatment for children impacted by PPP3CA.
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Join us today.
The PPP3CA Hope Foundation™ is the first parent-led non-profit with the mission to raise awareness, provide support for families impacted by PPP3CA, and promote and fund research directed towards a treatment for individuals with PPP3CA.​​
"Rare is many. Rare is strong. Rare is proud."
Rare Disease Day
Join us on the journey.
Science will find a treatment. Our kids are waiting.
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