Canadian Association of Psoriasis Patients

The Canadian Association of Psoriasis Patients (CAPP) is a national non-profit organization dedicated to improving the lives of Canadians living with psoriasis and psoriatic arthritis. Founded in 2012, the association provides evidence-based information, education, and support resources to patients and their families. CAPP advocates for equitable access to care and treatments by engaging with healthcare providers, researchers, and government stakeholders. As an affiliate of the Canadian Skin Patient Alliance, the organization plays a critical role in raising public awareness and reducing the stigma associated with chronic skin conditions.