The Leukaemia Foundation is a not for profit organisation focused on the care and support of patients and their families living with leukaemias, lymphomas, myeloma and related blood disorders.

The Foundation does this by providing counselling, accommodation, transportation and practical assistance for patients and their families. The Leukaemia Foundation also funds research into cures and better treatments for leukaemia and related blood disorders. 

The Leukaemia Foundation receives no direct ongoing government funding, and relies on the continuous support of individuals and corporate partners to expand its services.

Cystic Fibrosis (CF) is the most common life threatening genetic condition in Australia – and there is no cure. CF is a degenerative condition that affects many of the body’s systems, including the lungs and digestion. Children diagnosed with CF live through daily physiotherapy and medications, among other treatments, just to survive.

Money raised for clients provided a vast array of services nationally including providing emotional support to children, adults and their families through counselling, sibling activity days, and respite programs; practical support through equipment, hospital transfers, physiotherapy, accommodation, and special support for children during hospital stays; advocacy and education programs; and research.