What we do
Support
Our support groups are peer-led, meaning that the volunteers who facilitate the groups have BFRBs themselves. We provide a safe space to share experiences and seek advice from others who truly understand what it is like to live with BFRBs.
We also offer support for families, loved ones, and professionals who would like to learn more about how to care for people living with BFRBs in the UK, Ireland, and beyond.
Community
One of our main objectives is to grow and sustain the diverse community of people living with BFRBs across the UK and Ireland. We aim to bring people together through regular in-person and online support groups, social gatherings and special events, and to serve the community's needs through sharing research, resources, and advice.
We believe that building a compassionate community that everyone has access to is central to BFRB recovery.
Advocacy
Despite affecting approximately 5% of the population, BFRBs remain heavily stigmatised, misunderstood, and under-researched.
Through our advocacy efforts, we aim to increase awareness and understanding of BFRBs, especially in healthcare and school settings.
You can join our mailing list to keep up to date on our advocacy efforts.
Find Support
We provide informed, friendly support for people living with hair pulling disorder, skin picking disorder and other body-focused repetitive behaviours. Currently, all of our support groups and events take place online. For more information and to sign up for the Zoom link, click on the event you're interested in on the calendar below.
Announcing BFRB Con 2026
BFRB Con 2026 website is now LIVE!!
Please visit www.bfrbcon.org for all the information you need about BFRB Con 2026.
We're keen to hear from anyone who is interested in contributing to the scientific and community programme.
Registration will open in a few weeks.
We really hope lots of you will be able to join us!
