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Persons living with albinism in Uganda continue to face stigma, discrimination, and limited access to essential services. In the Elgon sub-region, advocates and community leaders are calling for greater awareness, equal opportunities, and stronger support systems to ensure that persons with albinism can live with dignity. In this feature story, we explore the challenges faced by individuals with albinism in eastern Uganda from discrimination in healthcare facilities and schools to persistent myths in some communities that continue to isolate families. Elizabeth Nekesa, founder of the Elgon Foundation for People with Albinism, shares her personal experience with stigma while seeking maternal healthcare and explains why community sensitization is critical. Meanwhile, Kapchorwa District coordinator Daniel Cherotich reveals the alarming number of children with albinism who have dropped out of school due to discrimination and lack of support. Health experts also break down the science behind albinism, explaining that it is a genetic condition inherited from both parents and not a curse or contagious disease helping to dispel long-standing myths that continue to affect many families. This story highlights the urgent need for inclusive education, improved healthcare access, and stronger community awareness to protect the rights of persons with albinism in Uganda. Story Compiled by: William Cheptoek Production: Uganda Radio Network Uganda Radio Network will continue following up on the fight for the rights and equality of persons with albinism in the country. Like Comment Subscribe for more updates, feature stories, and news from across Uganda. #Uganda #AlbinismAwareness #HumanRights #ElgonRegion #UgandaRadioNetwork #DisabilityRigh