The Aplastic Anaemia Trust is delighted to have partnered with Maggies to bring you a series of helpful webinars. Read more
On 20 August 2020, Dr Sujith Samarasinghe, consultant paediatric haematologist at Great Ormond Street Hospital, answered live questions from the families of children with aplastic anaemia. Hear his answers in full. Read more
Regular online meet ups, for advice and emotional support. Connect and share your experiences of coping with Covid-19. Read more
We're partnering with Maggie's to offer you a friendly mental wellness session via Zoom at 4pm every Wednesday Read more
Bringing failed bone marrow back to life
Help us reach and support everyone affected by aplastic anaemia, a life-threatening rare bone marrow failure, and to fund research into finding a cure that works for all.
Aplastic means your bone marrow is failing to produce enough of ALL essential blood cells
Join people just like you and find the support you need today!
We're looking for gorgeous gifts from small independent sellers, to give our Christmas Market a touch of magic! Here's how you can get involved...
The Aplastic Anaemia Trust is delighted to have partnered with Maggies to bring you a series of helpful webinars.
One of the effects of the coronavirus health crisis has been that AA patients who would otherwise be candidates for a transplant are unable to have one. Our patient advocacy on this issue has led to the drug eltrombopag being made rapidly available for these patients, and for severe AA patients who have previously failed to respond to ATG/ciclosporin.
I’m Ella and I was diagnosed with aplastic anaemia last year, at 17. My brother saved my life by donating his bone marrow. Read more
Friday 19th of August 2016. That’s when it all started, a date that will remain in my memory for the rest of my life. Read more
My name is Barbara, I'm 65 years young and I live in Dublin. I have been diagnosed with Aplastic Anaemia / MDS overlap. Here is my story. Read more