August 7, 2024
Newsletter (April – June 2024)
Petition to the World Health Organization (WHO) to Re-Add Sunscreen to the Essential Medicines List…
Read MoreThe Africa Albinism Network engages a wide range of actors, supporting national-level grassroots responses to attacks and discrimination throughout the African continent, resulting in local and regional impact.
0
0
0
We are a consortium of non-governmental organizations working to promote, through human rights advocacy, the dignity, rights, and welfare of persons with albinism in Africa and their family members.
Images on our website courtesy of © Patricia Willocq, Rick Guidotti, and JFMean.
We work with like-minded entities to prioritize human rights-based support for persons with albinism in Africa and influence action in response to the challenges faced by persons with albinism and their family members, through these three key vehicles:
We provide a rich library of more than 500 digital resources in different languages accessible to activists, researchers, the media, and other key stakeholders that can advance the movement for the promotion of human rights for persons with albinism.
Stay updated
Through stories of impact, AAN seeks to inspire our potential supporters, including donors, political leaders, and grassroots activists, among others, that it is urgent to implement national action plans on albinism to transform the lives of persons with albinism in Africa.
August 7, 2024
Petition to the World Health Organization (WHO) to Re-Add Sunscreen to the Essential Medicines List…
Read MoreAugust 5, 2024
A Message from our Executive Director In 2014, the United Nations declared June 13 International…
Read MoreJuly 8, 2024
The Africa Albinism Network at its Women’s Learning Forum, held from May 28th to 30th,…
Read More