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Thank YOU!

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Through these uncertain times, one thing is certain: The Progeria Research Foundation is still working tirelessly to help families impacted by Progeria. PRF is there for the children and their families from day one, so for this year’s ONEpossible Campaign, we reflect on…

A Parent’s Journey

Tina Pickard, mother of smart, active, 13-year-old Zach

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Click HERE to read more about Tina’s story.

[/et_pb_text][et_pb_text _builder_version=”4.4.7″]When PRF was founded in 1999, Progeria was completely uncharted territory. Families across the globe had no medical guidance, no researchers, and no hope for treatments or a cure. Thanks to YOUR support, PRF changed all that! Through the many programs that drive the research and guide the families, including diagnostics, clinical trials, and a treatment guidelines handbook, parents now have the support they need and the hope they dream of. [/et_pb_text][et_pb_text admin_label=”drug trial” _builder_version=”4.4.7″ text_text_color=”#ffffff” background_color=”#29327a” background_size=”initial” background_position=”top_left” background_repeat=”repeat” text_orientation=”center” background_layout=”dark” custom_margin=”10px|20px|5px|60px|false|false” custom_padding=”10px|20px|5px|60px|false|false” border_color_all=”#29327a”]

√ PRF’s trial drug lonafarnib is helping children and young adults
   with Progeria live longer, healthier lives
√ PRF continues our relentless search for the cure

… and it’s only possible because of YOU!

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Please help us continue our journey –
to help parents like Tina,
and cure kids like Zach.

Be ONE to make the cure POSSIBLE!

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