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The Progeria Research Foundation

For the Children ♥ For the Cure

Vision

Our vision is a world in which every child with Progeria is cured.

Mission

To discover treatments and the cure for Progeria and its aging-related disorders, including heart disease.

Vision

Our vision is a world in which every child with Progeria is cured.

Mission

To discover treatments and the cure for Progeria and its aging-related disorders, including heart disease.

Progeria is an ultra-rare, fatal, “rapid-aging” disease that afflicts children who, without the FDA-approved treatment lonafarnib, die of heart disease at an average age of 14.5 years. PRF is the only non-profit organization solely dedicated to finding treatments and the cure for Progeria, and is making phenomenal progress toward that goal.

News

NEWS RELEASE: FOR IMMEDIATE RELEASE

NEWS RELEASE: FOR IMMEDIATE RELEASE

The Progeria Research Foundation Celebrates 25 Years of Racing Toward a Cure 25th Annual International Race for Research Set for September 19, 2026, in Peabody, MA.
Come join us and hit the streets for the City of Peabody’s largest annual road race. We’re excited to mark this special milestone with our incredible community.

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ONEpossible 2026 Starting June 1 2026: Everywhere

ONEpossible 2026 Starting June 1 2026: Everywhere

Thank you to everyone who supported our 2026 ONEpossible Campaign! Every team crushed its goal, and your support is making a real difference by helping children and young adults with Progeria live longer, healthier lives. Together, we WILL find the cure.

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Get Involved

Our lonafarnib clinical trials enrolled 107 children from 42 different countries to test this now-FDA-approved treatment. Because of your support, these children and young adults are living longer, healthier lives.

About PRF

Your donation helps The Progeria Research Foundation treat children with Progeria today, and cure them in the future.

Meet the Kids

We hope their stories inspire you to support PRF, so those dreams can come true.

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