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Showing posts from December, 2017

Advocacy and media engagement: Creation of Awareness about the plight of children with albinism in Uganda.

SCOSP led a team that led to the arrest of the suspect, the children were rescued and evacuated. They later joined school and chance they ordinarily hadn't as their parents were not willing to support their education. They are now able to read and right due to the support of SCOSP. They never attended any form of education until SCOSP enrolled them into a safe school.    Children with albinism live in fear due to threats to their lives because they have a misunderstood condition of melanin deficiency. Many myths and ignorance about the condition have left the children and women women with albinism largely at risk of being mutilated, killed for their body parts to be used in magic rituals falsely believed to create wealth in magic concoctions by witch doctors who claim that they can create wealth out of that. Children and women with this condition have received threats from their parents and some members of the extended families. SCOSP continues to make tremendous mile stones

ADVOCACY FOR THE RIGHTS OF PERSONS WITH ALBINISM IN UGANDA

In the first quarter of 2017, SCOSP made a landmark when the first interface meeting was held in Kisoro District of south western Uganda. The meeting targeted people with albinism under SCOSP and the Kisoro District local government leaders, community leaders, and representatives from CSOs.  This was aimed at providing space for the children and caregivers of children with albinism to reframe the conversation around albinism and instigate lasting change. The leaders unanimously agreed to provide the necessary support always whenever we have advocacy activities. The chairman LC V  of Kisoro District hailed the work of SCOSP and  pledged to always participate in the NGO activities in his district. He promised to take advocacy issues that were raised by people with albinism to the District council for further discussion and where possible amplify the voices of people with albinism in Kisoro at a higher level.  By Michael Sabiiti, Founder and Executive Director.