PAK is creating hope.
Patient-led, uniting patients, caregivers, and healthcare professionals.
The Psoriasis Association of Kenya is a patient-led organization uniting patients, caregivers, and healthcare professionals. Focused on the wellbeing of people living with psoriatic disease and their caregivers, we create hope, advance education by raising awareness and sharing knowledge, strengthen advocacy, and ensure access to care for all.
Built by people living the experience, with caregivers and clinicians walking alongside them.
Safe spaces for honest conversations, practical guidance, and connection that reduces isolation.
Trusted public awareness and healthcare engagement that challenge myths and improve care.
Stronger pathways to diagnosis, treatment information, and dignity in the health system.
Psoriatic disease is a systemic inflammatory condition, not just a skin disorder. It is a chronic autoimmune disease that occurs when the immune system becomes overactive, causing skin cells to build up too quickly and triggering inflammation throughout the body. It is not contagious; you cannot catch it from another person.
Psoriatic disease affects the skin, joints, and overall wellbeing.
It cannot be spread through touch, utensils, or close contact.
It requires ongoing management, support, and informed medical care.
Stigma, pain, and mental health challenges often go unseen.
Awareness and outreach, patient support, and education and advocacy shape how PAK serves patients, caregivers, and healthcare professionals across Kenya.
Leading public campaigns to educate communities and dispel myths, working with media, healthcare providers, and community leaders.
Providing resources, peer support, and connection opportunities. Through events and discussions, we build empowered communities.
Advocating for better healthcare training, earlier diagnosis, and inclusive policy development to ensure respect and care for all.
Membership is open to patients, their caregivers, and healthcare professionals. Together, we ensure no one walks this path alone.
Join for peer support, trusted updates, advocacy opportunities, and a direct path into PAK's support channels.
Access to peer support groups and forums where patients and caregivers can speak openly.
Latest medical research, care tips, training opportunities, and practical guidance.
Patient testimonials, lived experience, and advocacy stories that drive change.
Real patient voices sharing journeys of resilience, breaking stigma, and living with dignity.
Joining PAK was the first time I realized my skin did not define my future. The community gave me the confidence to seek modern biologics and return to my career in Nairobi.
For years, people told me it was a "curse". PAK educated my family and my coworkers. Today, I advocate for others so they do not have to hide like I did.
We collaborate with global patient networks to amplify Kenyan voices, share proven advocacy tools, and strengthen access to care.
Nairobi will host IFPA Forum Africa from May 7-9, 2026, bringing training, workshops, and regional dialogue to Kenya.
Explore stories, campaigns, member meetings, and the patient voices helping reshape public understanding of psoriatic disease.
Membership is open to patients, caregivers, and healthcare professionals who want support, training, and advocacy connection.