Super Rare 2022 resources

Be Super Rare! People with rare bone marrow failure come together to raise funds and spread the word about the issues that matter to people with aplastic anaemia. Because we are stronger together. Read more

Request a callback

Request a callback from one of the team. Read more

Winter Wellness

Our new programme of events, publications and activities designed to lighten the darkest months. Stay safe, happy and healthy this winter. Our Winter Wellness programme is funded by The National Lottery Community Fund, Sobi and Alexion, AstraZeneca Rare Disease (who have sponsored our Winter Webinar series). Read more

Double Birthday Club resources

When you have a bone marrow or stem cell transplant, you can choose to celebrate that as a new birthday! Read more

AA Voices: personal stories

Aplastic anaemia is different for everyone. Read blogs and watch videos about the real experiences of members of our community. Read more

In loving memory of Yas Yadi

A book of condolence, in loving memory of Yas Yadi Read more

Ask Daniel

Daniel is here to answer your questions from a patient's perspective! Read more

Support Line

If you or someone you know has been diagnosed with aplastic anaemia, we are here to help. Read more

Coronavirus vaccines - your questions answered

Do you have a question about the COVID-vaccine in relation to aplastic anaemia? Here, we've answered some of the more common questions asked by our community. Read more

Our shop

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. Read more