Psoriasis looks different on Black skin. Together, we educate, support, and advocate for dignity and care.
Founded in 2004, the Psoriasis Association of Kenya (PAK) is a patient-led organization advocating for the rights and wellbeing of those living with psoriatic disease. What began as a small initiative has grown into a national voice, breaking stigma, multiplying voices, and connecting patients, caregivers, and healthcare professionals across Kenya.
To educate and advocate through empowerment, reassuring patients and caregivers, strengthening professional advocacy, and ensuring that no one living with psoriasis walks alone.
A future where people living with psoriasis in Kenya enjoy dignity, optimal health, and a stigma-free life.
Strengthening support for patients and caregivers through connection, events, and practical help.
Raising public understanding to dispel myths and combat misdiagnosis.
Ensuring better access to care and informed policy development nationally.
Wellness initiative with nature walks, games, and outdoor bonding for community healing and resilience.
Focused on the role of family support at Kenyatta National Hospital.
Highlighted arthritis, cardiovascular disease, and mental health at the Public Service Club.
A preview of community initiatives across Kenya.
Explore Vimeo highlights that capture PAK's patient leadership, advocacy, and awareness work.