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Who We Are

Lupus Foundation of Africa

The Lupus Foundation of Africa (LFA) was founded in 2013, seeking to improve awareness of lupus among both health professionals and the general population, as well as to provide a community of emotional and material support to people diagnosed with lupus. With more than 90 active members across East Africa, we are ready to grow our community of warriors and highlight the importance of affordable diagnosis and treatment options, while reducing the stigma and lack of awareness of the disease.

Our

VISION

To achieve a world where people with lupus can live full and active lives.

Our

MISSION

To empower people by providing information about lupus and offering support, so their voices are heard and their condition diagnosed and managed effectively.

Our

VALUES

  • We believe in improving the lives of people who have lupus
  • We believe that lupus patients are entitled to specialised care and treatment
  • We believe that lupus patients are entitled to the best possible information about their condition
  • We believe in informing and educating the medical profession and the public about lupus and its effects
  • We believe in bringing people with lupus together so they are not isolated
  • We believe in listening to people who want to talk about lupus

Our Objectives

Awareness

To improve awareness of lupus among the general population

Support

To provide a community of support for people diagnosed with lupus and their families

Diagnosis

We increase the rate of diagnosis and improve the quality of treatment