Aplastic Anaemia is a very rare condition, but you can help us make patients feel special - not alone. Help us raise funds and awareness this Rare Disease Day and be Super Rare! Read more
Browse our brand new resources for children and young people affected by aplastic anaemia, and their families and friends. Read more
Information for individuals with aplastic anaemia and their families to help prepare for the cold season Read more
We are fuelled by our desire to find a cure for aplastic anaemia and support everyone affected. Click and watch a video about who we are Read more
Bringing failed bone marrow back to life
Aplastic Anaemia is a very rare condition, but you can help us make patients feel special - not alone. Help us raise funds and awareness this Rare Disease Day and be Super Rare!
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!
You deserve some cheerful post! Order free booklets and leaflets, for aplastic anaemia patients of all ages and their families and friends. Browse our range of beautiful cards and gifts - chosen with care to delight our community and raise valuable funds.
Browse our brand new resources for children and young people affected by aplastic anaemia, and their families and friends.
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
We're partnering with Maggie's to offer you a friendly mental wellness session via Zoom at 4pm every Wednesday Read more
Regular online meet ups, for advice and emotional support. Connect and share your experiences of coping with Covid-19. Read more