There are times when Hugh McClure feels like screaming from the rooftop, so that everyone can know about the wonderful person that his dad was, and how much he misses him.
Leukaemia Foundation Blood Cancer Support Coordinator Shirley Cunningham shares some insight for those who are ready to start dating after loss.
Bridget Swee honours her husband's legacy by sharing their story and how her family is starting to find their feet in a world without him.
Trish Wilson has "always been drawn to working in areas where loss has been an underlying issue”.
In this Q&A, counsellor, Trish Wilson, was asked to share her experience and knowledge to answer some of the most asked questions around grief and loss.
Although never touched personally by blood cancer, David Pratt was so moved by the stories of families battling the disease that he has made the ultimate commitment to improve their future with a gift in his Will.
To mark World Blood Donor Day on June 14, Jessica Lake shares how her now six-year-old son, Larry, depended on the kindness of blood donors for over a year after being diagnosed with the rare blood disease, aplastic anaemia.
Tony Wakely’s diagnosis with MDS quickly transformed to AML, which he beat with a transplant. But a year later, he was shocked to find out his MDS had come back.
Two new international clinical trials are expected to improve access to new therapies for Australians with MDS as part of the Leukaemia Foundation’s Trials Enabling Program (TEP).
The Leukaemia Foundation provided consumer comments to the Pharmaceutical Benefits Advisory Committee (PBAC) in relation to Otsuka Australia Pharmaceutical’s resubmission for decitabine and cedazuridine (Inqovi®) for high-risk MDS and CMML.
