Who we areCASA was formed by a group of frustrated but determined individuals with different scarring alopecias who wanted to share their experiences with this life-changing disease.
We recognized that there was no Canadian outlet to share what limited knowledge there is about scarring alopecias and we wanted to talk to people who can empathize and actually understand the challenges we face.
We are women and men of all ages living with LPP, FFA, and CCCA, discoid lupus, pseudopelade, folliculitis decalvans and dissecting cellulitis. We are looking for answers. We are looking for connections. We are looking for ways to cope. We are looking for treatment options. We are determined to find them. In the meantime, we will stay hopeful. Together.