The Association Franco Congolaise du Vitiligo is a patient support organization based in the Democratic Republic of Congo (DRC), dedicated to improving the lives of individuals living with vitiligo and their families. The Association’s foundational mission is to offer comprehensive support, raise awareness, and build community connections for those affected by vitiligo throughout the country.

A key initiative undertaken by the Association is a collaborative program with the Ministry of Health aimed at identifying and registering vitiligo patients across the DRC. This effort seeks to create an accurate national database, which is essential for understanding the prevalence of the condition, informing healthcare planning, and improving patient care.

Through this partnership with government authorities, the Association advocates for greater recognition of vitiligo as a medical condition that requires specific attention and resources. It strives to break down stigma by educating the public and fostering acceptance of people with vitiligo.

The Association also supports patients and families by providing information, emotional support, and access to community resources. Though still developing, it aims to expand its reach through ongoing programs that promote education, social inclusion, and access to treatment.

With its strategic focus on patient registration and collaboration with health officials, the Association Franco Congolaise du Vitiligo is laying vital groundwork for a more inclusive and informed healthcare system in the DRC, one that acknowledges and meets the needs of people living with vitiligo.

The organization actively engages with its community via social media, helping to connect individuals and spread awareness.