A Significant Meeting for the LFF
The Lupus Foundation of Fiji was granted an audience with the Minister for Health and Medical Services – the Honourable Dr. Ratu Atonio Lalabalavu (2nd from left) in April 2023. The Executive Director of the LFF – Ms. Una Tuitubou (2nd from right) and her Deputy – Mr. Kaliova Turagaiviu (far left), were both accompanied by two of our Trustees – Ms. Luisa Vodonaivalu (3rd from left) and Mr. Ernest Bogi Basilio (far right) met with the honourable Minister at the Ministry HQ – to discuss the way forward for the Foundation, after it’s launch in May 2019. This meeting resulted in the signing of an MOU with the Ministry of Health and Medical Services in October 2024. The Lupus Foundation of Fiji is forever grateful to the government of Fiji, for coming on board and joining us – in this fight against this auto-immune disease, commonly known as “Lupus”.
Risk factors for developing lupus
The triggers for lupus are poorly understood. Some factors that are associated with developing lupus are:
- Being female: 90 per cent of Pacific Islanders with lupus are women.
- Early adulthood: most cases of lupus are detected in people aged between 15 and 40.
- Genetic susceptibility:lupus is more prevalent in some families and some racial groups. Lupus is more prevalent and more severe in.
- Sunlight exposure can be a trigger in susceptible people.
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AWARENESS
ABOUT US
The Lupus Foundation of Fiji (LFF) is a ‘not-for-profit’ charitable organisation that was established here in Fiji, to address any issue relating to this Auto-Immune Disease, which has been around the world in most developed countries, since the 13th century!
The Lupus Foundation of Fiji (LFF) was established by a group of ‘like-minded’ people, who have been affected directly and/or indirectly by this disease.
Lupus Fiji Database
Information is essential to creating awareness around Lupus as well as when trying to raise concerns to relevant stakeholders to help improve the care and support for those living with Lupus in Fiji.
The foundation is collecting information today to be able to talk about the dynamics of Lupus affecting the people of Fiji with supporting information to address areas of concern constructively.
Your participation in building this database is valued and appreciated.
The database is also for Friends and Family members of those with Lupus. This will enable the foundation contact you as well.
Useful resources
For more information, we recommend visiting the National Resource Center on Lupus