Women disproportionately affected by lupus in Fiji, Minister highlights

Women in Fiji, particularly indigenous iTaukei women, are disproportionately affected by lupus, according to Sashi Kiran, the Minister for Women, Children, and Social Protection. Speaking at a fundraising event for the Lupus Foundation of Fiji, Kiran stressed the critical need for increased awareness, earlier diagnosis, and robust community support for those living with the chronic autoimmune disease.

Kiran described lupus as an "invisible disease" where symptoms like extreme fatigue, fever, and joint pain are often dismissed or mistaken for stress or common ailments. This misunderstanding frequently leads to delayed diagnosis and treatment. She also raised concerns about the stigma and lack of understanding surrounding lupus and other chronic illnesses, which can deter individuals from seeking necessary medical help.

To address these issues, the Ministry of Women, Children, and Social Protection is prepared to partner with the Lupus Foundation of Fiji. The collaboration aims to incorporate lupus awareness into existing outreach programs and enhance support systems for patients and their families. The Minister also called for more localized research to better understand the disease's specific impact within Fiji and to strengthen support services.

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The Ministry is prepared to work closely with the Lupus Foundation of Fiji to incorporate lupus awareness into existing outreach programmes and improve support for patients and their families.

The Minister commended the Lupus Foundation of Fiji and its founder, Unaisi Tuitubou, for their advocacy efforts. Kiran acknowledged Tuitubou's transformation of personal loss into a supportive movement for lupus patients, providing hope and demonstrating that individuals do not face the disease alone. The government reaffirmed its commitment to initiatives promoting lupus awareness, research, and community education.

Kiran urged Fijians to approach individuals with lupus with greater understanding, dignity, and compassion. The call for action underscores the importance of public education in managing the challenges posed by the disease and supporting affected communities.

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Tuitubou’s courage and commitment have given hope to countless families and helped many people realise they are not facing the disease alone.