Who we are

We believe that there is a number of Rwandans suffering from psoriasis in silence.
Our works is:

Rwanda Psoriasis and Psoriatic Arthritis Association
  • Educating the patients and public alike about psoriasis with its physical and psycho-socio-economic effects on its patients. A more informed community can yield more opportunities and better living conditions for patients.
  • Linking the economically challenged patients to institutions who can fund their medicines and treatments.
  • Providing a community for the sufferers that can guide them to having a good sense of being through emotional support.
  • Linking new patients with no doctors managing their conditions to proper and qualified medical practitioners.
  • Working continuously with Ministry of health seeking ways on how to include psoriasis into the national health policy and agenda of the government.
  • Helping to create a national psoriasis registry.
  • Providing a venue for sharing knowledge among psoriasis experts for the discovery of new and better treatments
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