18th May saw key clinicians and patients join together at the James Black Centre at King's College Hospital to share and hear updates on the latest clinical trials. Read more
On May 7th, the people of Wales go to the polls to elect new members of the Welsh Parliament. This election is an opportunity for those impacted by aplastic anaemia to raise the vital issue of fair access to medications for those living with rare diseases. Read more
We've moved some things around... Read more
For over 40 years, we’ve been working to change the story for people affected by aplastic anaemia. And the progress we’ve made - from life-saving research to vital patient support - has only been possible because of those who came before us, and those who have chosen to leave something behind. We're recently launched a free Will writing service, we’re asking: What will your legacy be? Read more
How gifts in Wills help families like Fiona’s... Read more
It’s all change at The AAT as we bid a sad goodbye to Stevie Tyler as our CEO, and hello to incoming CEO, Joe Kirwin. We catch them in conversation about how The AAT has grown under Stevie’s leadership, and where we might go next, with Joe in charge. Read more
The NHS website for Scotland publishes three pages of expert content about aplastic anaemia. Read more
Families had a fab time on our London Wildlife walk - with huge thanks to London Wildlife Trust for welcoming us to Walthamstow Wetlands. Read more
Lockdown didn’t stop Caden Moore and his intrepid family from celebrating three years since his bone marrow transplant with an epic adventure challenge to travel 530K! Read more
The AAT have awarded a two-year grant to the internationally renowned haematology research team at King's College London and King's College Hospital, enabling the identification and relevance of novel somatic mutations in aplastic anaemia Read more
The Aplastic Anaemia Trust announce the award of a research grant to Great Ormond Street Hospital, to further the understanding of aplastic anaemia in children across the UK Read more
Here at the AAT we keep spreading awareness of aplastic anaemia and other rare bone marrow failures, and why research is so important. Read more
Helpful information for patients diagnosed with aplastic anaemia and going into hospital for a course of anti-thymocyte globulin (ATG) Read more
Grazina, the AAT's CEO, finds good coverage of key issues at the annual Rare Disease UK meeting on 13 June Read more
Our loyal supporters turn up in droves in aid of the Aplastic Anaemia Trust for our annual flagship walk in the park on Saturday, 9 June 2018 Read more