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🌏 As of September 2025, this is where the 153 children and young adults with Hutchinson-Gilford Progeria Syndrome (HGPS) live, all with a progerin-producing mutation in the LMNA gene; and 82 people in the category of progeroid laminopathy (PL), who have mutations in the lamin pathway but do not produce progerin; in a total of 51 countries. Want to learn more? Visit our Find the Children website page: https://www.progeriaresearch.org/find-the-children/ 💙 Help The Progeria Research Foundation (P
0:31
🌏 As of September 2025, this is where the 153 children and young adults with Hutchinson-Gilford Progeria Syndrome (HGPS) live, all with a progerin-producing mutation in the LMNA gene; and 82 people in the category of progeroid laminopathy (PL), who have mutations in the lamin pathway but do not produce progerin; in a total of 51 countries. Want to learn more? Visit our Find the Children website page: https://www.progeriaresearch.org/find-the-children/ 💙 Help The Progeria Research Foundation (P
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Tiffany Wedekind lives with a rare genetic disease called progeria that causes rapid aging. She joined DBL and opened up about the frustrating road to her diagnosis, how the frequent awareness of mortality has changed her life, and how the death of her brother, who also lived with progeria, motivated her to start her own business. Check out Tiffany's studio at https://www.wanderlustcbus.com/ #TiffanyWedekind #Progeria #aging #mortality | Daily Blast LIVE
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