Persons with albinism urge government for specialised healthcare and tax-free sunscreen

People living with albinism in Uganda are urgently appealing to the government to establish specialised healthcare services in public health facilities. Representatives argue that limited access to proper medical care, sunscreen lotions, and protective clothing exposes vulnerable individuals to severe skin and eye complications.

Speaking at a media briefing in Kampala, Ms Faith Bwanika, secretary of the Matayo Foundation, emphasized that services for persons with albinism should be integrated into public institutions ranging from Health Centre IVs up to Mulago National Referral Hospital. She stressed the necessity of regular medical assessments to catch early signs of sun damage.

Organisers highlighted that the rising intensity of ultraviolet radiation makes items like sunscreen, hats, and sunglasses essential rather than optional. However, many citizens struggle to afford them due to high costs. Advocates have pointed out that tax-relief proposals for these protective products have unfortunately stalled since the tenure of former Speaker Rebecca Kadaga.

Senior journalist Solomon Kaweesa, who is spearheading an upcoming fundraising dinner in partnership with the Matayo Foundation, noted that charity efforts alone cannot cover the massive nationwide need. The upcoming event, scheduled for November 27, 2026, at Pope Paul Memorial Hotel, aims to raise resources to establish a dedicated one-stop center and provide practical skills training for economic independence.

Leaders also underscored the critical role of families in accepting children born with albinism and shielding them from hazardous weather exposure. Corporate organisations were further urged to offer equal employment opportunities to help combat social isolation and discrimination.

Read more details in the Daily Monitor report.