Where it began…
The TLC Foundation for BFRBs was in 1991 and is dedicated to educating and supporting individuals, families, researchers and clinicians about Body Focused Repetitive Behaviors.
They have a plethora of resources and connect support groups and therapist to individuals seeking help through their BFRB journey.
TLC continues to engage with the community through virtual events, social media and free videos on YouTube.
Have fun, meet new friends, and learn origami!
Origami Story Club is for kids ages 6-11 with a BFRB.
Our very own BFRB Mom co-host, Jen, is the fabulous person behind OSC. Jen is vibrant, caring and the BEST cheerleader! We have seen first hand her amazing power to engage with kids of all ages. Her worldly perspective is always a breath of fresh air, and inspires us to harness our own super powers.
Founded in August 2016 through the efforts of CEO Lauren McKeaney,
Picking Me Foundation NFP is the only donor-supported nonprofit dedicated to advocating Dermatillomania (Skin Picking Disorder) for sufferers, supporters, and educational communities alike, encouraging individuals to choose themselves over the mental illness that chose them by
#PickingMe over Skin Picking
Skin Picking Support is an online community for people with excoriation disorder that provides resources to educate and spread awareness for body-focused repetitive behaviors (BFRBs) while offering insight into Angela Hartlin’s recovery journey.
