After losing her dad to MDS, and her brother’s diagnosis just a month before hers, Christine Heath’s family underwent genomic testing to understand whether their MDS could be hereditary.
Basit Salik, Dr Jamie Kuzich and Dr Julian Grabek are the successful recipients of the 2021 PhD Scholarships.
Jennie and Russell Wigginton were planning for baby number two, when Jennie was diagnosed "out of the blue".
Professor David Ross discusses the "massive explosion" of recent clinical trial activity in MPN.
Dr Liesl Butler is investigating the gene mutations and biological pathways that lead to the development of MPN.
Meet Tereena Cocks, who has practised meditation and visualisation almost as long as she’s been living with blood cancer – nearly half her life.
Veteran traveller Bryan Mitchell, get treatment for his MDS as he journeys from country to country… until COVID-19 put a stop to his travels.
Seven years after being diagnosed with PV, Ken’s spleen suddenly ruptured.
How the MPNs are classified is set to change with eight new classifications based on the underlying mechanisms that drive the mutations.
