The Eczema Society of Kenya (ESK) is a leading patient-led, non-profit organization committed to improving the lives of people living with eczema, skin diseases, STD's and other related health conditions through advocacy, education, research, patient empowerment, and strategic partnerships.
Established to champion the rights and wellbeing of patients, ESK has grown into one of Africa's respected patient advocacy organizations, working at the intersection of healthcare, policy, research, and community development. We believe that every person deserves equitable access to quality healthcare, evidence-based information, timely diagnosis, effective treatment, and the opportunity to live with dignity.
Our work is guided by patient experiences, scientific evidence, and meaningful partnerships with governments, healthcare professionals, researchers, academia, civil society, and international organizations. Through innovation and collaboration, we continue to influence policies, strengthen health systems, and improve patient outcomes across Kenya and beyond.
To improve the quality of life of individuals and communities through patient-centred advocacy, health literacy, research, education, partnerships, and policy influence in the prevention and management of chronic diseases and other public health priorities.
To create a society where every person affected by skin diseases has access to quality healthcare, accurate information, effective treatment, and the opportunity to live a healthy, productive, and dignified life.
The Eczema Society of Kenya works with internationally recognized organizations to strengthen patient advocacy, promote research, build leadership, and improve access to quality healthcare.







