Fijians are being encouraged to use local narratives and languages to foster a deeper understanding of albinism and dismantle the stigma faced by children living with this condition. This call to action was made by Sashi Kiran, Minister for Women, Children, and Social Protection, during an event marking International Albinism Awareness Day in Lautoka.
Minister Kiran pointed out that many children with albinism continue to experience teasing and discrimination, primarily due to fear and misconceptions rooted in traditional beliefs and myths. She clarified that albinism is a natural hereditary condition that impacts melanin production, leading to lighter skin, hair, and eyes, as well as potential visual impairments.
Emphasizing the importance of compassion and acceptance, Kiran urged parents and educators to model kindness and respect for differences. She stated, “We must teach our children love, kindness, and compassion in all circumstances.” This approach is crucial, as children often mimic adult behavior in their interactions with others.
Additionally, the Minister highlighted Fiji’s proactive steps through its Albinism Support Program, which provides free sunscreen, glasses, and medical care. Despite these efforts, many individuals with albinism face barriers in accessing necessary support, with only about 200 out of an estimated 700 individuals seeking medical assistance.
Kiran’s statements reflect a broader need for education and awareness regarding various health conditions and disabilities in Fiji. Similar efforts have been observed in discussions on child abuse and neglect, as well as in addressing the health challenges presented by conditions like lupus and pediatric cancer, where stigma and misinformation can hinder proper care and support.
The hope remains that through community education and compassionate engagement, Fiji can foster a more inclusive environment that recognizes and supports the unique needs of individuals with albinism and other health challenges.
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