06/19/2026
π©΅ The future you make possible: a world where Progeria is curable.
Because of YOU, children with Progeria have grown into young adults. Your support helped bring lonafarnib, the first FDA-approved, life-extending treatment for , to the children who need it most.
Now it is time to take the next step.
The Progeria Research Foundation (PRF) and the Progeria Gene Team have developed SamPro-2, a gene editing therapy that, in mouse models, has permanently corrected the exact DNA error that causes Progeria. PRF is now advancing SamPro-2 toward human trials!
Dr. David Liu, Broad Institute, PRF Gene Team member, 2025 Breakthrough Prize Recipient, and upcoming 2026 PRF S.A.M. Award Honoree, says it best:
"The hope of our team is to use base editing to fix the root cause of Progeria, providing a pathway to a potential cure as well as advancing treatments for millions of other children with fatal genetic diseases."
This is the moment everything changes. And YOU can be ONE to change it.
Please donate today and share this post. Every dollar, every share brings us closer to a cure. π©΅
β‘οΈ https://bit.ly/OP2026Main
I'm fundraising for Progeria Research Foundation. It's an amazing organization. Everybody please check out my campaign! Find out more and donate here: https://fundraise.givesmart.com/vf/FINDTHECURE