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."
Wow, I love seeing the TLC Foundation getting the recognition it deserves in The New York Times! It’s amazing how awareness can spark change. This reminds me of my experience with FNAF game—sometimes you just need to keep rolling with the ups and downs, much like overcoming challenges in life. Keep up the great work!
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