Bhaskar Majumdar and his daughter, Urvi Majumdar, share their experience with blood cancer and the profound impact it had on their lives.
The Leukaemia Foundation and Haematology Society of Australia and New Zealand (HSANZ) have again partnered to award three of Australia’s brightest blood cancer researchers and clinicians with PhD scholarships
The Leukaemia Foundation welcomes the Australian Government’s decision to ban the use of adverse genetic testing results in life insurance.
Leukaemia Foundation staff come together to raise awareness for the Australian Bone Marrow Donor Registry (ABMDR), and the need for more Australians to register
After living with the disease for almost the entirety of her teenage and adult life, 23-year-old Siobhan Hoy is no stranger to the long-term side effects of blood cancer.
Michael Burridge candidly shares his experience living with blood cancer and the emotional and physical journey following his diagnosis with myeloma.
Rosie Proctor had just moved in with her partner and was living out her dream career as a nurse on the Gold Coast. Then a shock blood cancer diagnosis turned her from caregiver to patient at the very hospital where she worked.
Australia is facing a critical shortage of registered stem cell donors – and the solution lies in the hands of younger Australians.
Siobhan Hoy discusses her experiences living with blood cancer and the aftermath of her treatment, including the challenges she faced, such as the development of graft versus host disease.
The Leukaemia Foundation debunks the biggest myth surrounding one of Australia’s deadliest cancers to help save more lives.