47 people in Fiji have hemophilia, a rare blood disorder

There are 47 people in Fiji living with hemophilia, a serious genetic bleeding condition that can lead to life-threatening complications.

This was revealed by the Fiji Hemophilia Foundation during World Hemophilia Day at the Sigatoka Subdivisional Hospital, where they stressed that as of 2023 over 100 people have hemophilia but only 33 registered cases.

Hemophilia is caused by a deficiency of the clotting protein factor VIII and can occur in individuals without a family history.

Assistant Minister for Health and Medical Services, Penioni Ravunawa emphasised the crucial role of organizations like the World Hemophilia Foundation in raising awareness and providing support for those affected by hemophilia.

The Fiji Hemophilia Foundation offers critical support by providing free Recombinant Factor VIII lifesaving treatment to patients at major hospitals and health centres.

Symptoms include excessive bleeding, deep bruising, and joint pain, which should prompt immediate consultation with healthcare providers.

The Foundation is also collaborating with the Ministry of Health to streamline diagnostic processes and improve training for Emergency Department staff, ultimately enhancing patient outcomes.