- Representation: Through the People of Colour campaign, PAK showed the world how psoriasis appears on darker skin tones and why visibility matters.
- Empowerment: Sharing lived experiences helps patients speak openly, advocate for better care, and inspire others.
- Education: Policymakers, doctors, and families learn from real voices, not just medical definitions.
- Solidarity: Global campaigns connect Kenyan patients to a wider movement for equity and dignity.
Stories
Real voices. Real journeys.
Stories of resilience, advocacy, and hope from Kenyan patients, families, and the wider PAK community.
Section 1
Why stories matter
Stories are powerful. They break stigma, empower patients, and help communities understand that psoriasis is more than a skin condition.
Section 2
Patient voices
Nyawira Munyiri - Psoriasis Association of Kenya
"Psoriasis spread to 96% of my body. For years, I felt isolated. Through PAK, I found community and hope and now my story is part of a global conversation."
- Nyawira has lived with psoriasis for over 20 years, facing stigma and misdiagnosis.
- Her testimony was featured in a BBC programme highlighting how psoriasis looks different on darker skin tones.
- She advocates for visibility, equity, and dignity for patients of colour.
- Her story connects local Kenyan experiences to global campaigns like People of Colour.
Share your story with PAK.
Join a support group.
Volunteer for awareness campaigns.
Partner with us to amplify patient voices.
Section 3
Campaign highlights
PAK's campaigns bring psoriatic disease out of the shadows, from community talks in Kenya to global solidarity initiatives.
- Media campaigns on radio, TV, and social media amplify patient voices nationwide.
- Domino Effect 2025 showed how psoriasis triggers a chain reaction of physical, mental, and social challenges.
- Kenyan patient testimonies highlighted the African experience in global advocacy spaces.
- Dr. Hoseah Waweru Solidarity Fund (IFPA).
- PsorAfrica Alliance.
- GlobalSkin Impact Fund.
- People of Colour campaign.
Section 4
Member meetings and support
Beyond campaigns, PAK provides direct support to members so patients and caregivers feel connected and empowered.
Patients gather to discuss treatment challenges, stigma, and coping strategies.
Dermatologists, psychologists, and advocacy leaders bring expertise into community spaces.
Small group sessions offer safe spaces to talk about flare-ups, mental health, and family life.
Active WhatsApp groups connect patients across Kenya for daily tips, encouragement, and treatment updates.
Meetings often link to larger campaigns such as World Psoriasis Day, keeping advocacy alive between events.
Together, we can change the story of psoriatic disease in Kenya.
Join PAK, share your story, support advocacy, and stay connected through our community channels.