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The TLC Foundation was featured in The New York Times!

Apr 24, 2025
1 min read

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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77 Comments


alisacarlos
Oct 14

It’s great to see organizations raising awareness and sharing information through trusted platforms like The New York Times. Bringing more attention to important topics can help people better understand different experiences and find support. It’s interesting how online communities also connect people with different interests, from awareness campaigns to fashion pieces like the adidas mexico jacket.

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My Local Place
Oct 09

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Black Bear
Oct 06

This article is a valuable resource for raising awareness and helping people better understand BFRBs. For readers who also enjoy creative writing and typography, a Cursive Font Generator can be a simple tool for experimenting with different text styles and handwritten-looking designs.

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starlias123
Sep 11

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recorder
Sep 10

 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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