From real patient stories to tips on living well, hear firsthand from people who have faced blood cancer.
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In February 2021, Lorie Sarson was diagnosed with anaplastic large cell lymphoma (ALCL), putting her and husband Troy in immediate financial distress due to treatment and transport costs.
When Julie Allen was diagnosed with lymphoma as a young professional mum, she thought she'd go straight back to work after treatment. But afterwards she literally felt “stripped bare”.
Adelaide man Graham Lewis had two stem-cell transplants and was left with severe graft-versus-host disease. He believes the existence of OCPs would have greatly improved his quality of life.
Dr Piers Blombery explains the basics of molecular testing which informs the treatment of blood cancer.
Julian Lindsay’s goal is to set up an international study aimed at improving survival and quality of life through drug optimisation.
An Australian study will examine the immune response to the COVID-19 vaccine in patients with the low-grade non-Hodgkin lymphomas.
Associate Professor Michael Dickinson says CAR T-cell therapy is a 'revolutionary step forward'.
We stand with Indigenous Australians to close the gap in health. We know we need to do better for our First Nations people living with blood cancer.
Blood cancer survivor and midwife, Catherine Wheeler shares her experience being eligible for the Phase 1a COVID-19 vaccine rollout.
When diagnosed with a blood cancer as a young adult, Vicky Pellowe struggled to find the relevant information she needed to manage her diagnosis and live well as a survivor.
Patrick won't let his lymphomas stop him from achieving his two milestones - to walk 10 kilometres, and to swim 200 metres butterfly!
“COVID’s been good to me and quite a few other patients”, says Andrew Warden, who volunteered to be a “guinea pig” on a program initiated by Professor Judith Trotman.
