The TLC Foundation was featured in The New York Times!
- TLC
- 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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What an inspiring feature — it’s wonderful to see such meaningful work highlighted so prominently. Your dedication truly makes a difference, and it reminds me how vital support systems are for creators everywhere. As someone connected with Ireland’s book printing & binding service, I appreciate how stories and resources like this empower voices and strengthen communities.
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It's wonderful to see the TLC Foundation highlighted in The New York Times, such articles truly contribute to increasing understanding and awareness. It made me realize how crucial it is to communicate clearly and professionally, just as having a solid CV and cover letter may make all the difference. A professional CV and cover letter writer can significantly improve your job applications if you need assistance crafting a compelling CV and cover letter.
I’m really glad to see the TLC Foundation and BFRB experiences featured in The New York Times 99 nights in the forest — increased awareness in a major outlet can make a huge difference in reducing stigma and helping more people find support.