The TLC Foundation was featured in The New York Times!
Updated: Jun 10, 2025
Chloe Shakin interviewed nearly a dozen individuals with BFRBs, and experts who specialize in their treatment, for this article 👉 https://www.nytimes.com/2025/04/18/well/skin-hair-picking-dermatillomania.html?unlocked_article_code=1.Ak8.qfzG.KXAz6jT_OUcZ&smid=url-share
"But the secrecy has made it difficult for many people with BFRBs, which affect at least 3 percent of the world’s population, to heal. “It’s hard to go forward if you’re so stuck in shame that you can’t talk about it to anyone,” said Suzanne Mouton-Odum, a psychologist who specializes in treating the issue and works with a nonprofit that supports people with BFRBs."
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Such meaningful press coverage for the TLC Foundation! This New York Times feature does vital work shining light on BFRBs and the shame many affected people experience. It is incredibly valuable to bring these often‑overlooked struggles into mainstream public conversation. Huge congratulations to everyone at TLC for this well‑deserved recognition and for your ongoing advocacy work. --recordly
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It's great to see the TLC Foundation getting recognition for their work with BFRBs. The New York Times article sheds light on an issue that many people struggle with but rarely discuss. For more resources and support, you can visit free spot the difference worksheets pdf.