Every child and young person diagnosed with aplastic anaemia deserves the best treatment, care and chances of leading a full, and enjoyable life Read more
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Social media graphics for you to use to support your Super Rare fundraising. Read more
Employment Lawyer Carolyn Miller gives a summary of your rights at work under the discrimination act, how to tell if you're facing discrimination and what to do about it. Read more
Are aplastic anaemia patients more at risk, and will the pandemic affect their treatment? Read more
The latest updated guidance on shielding and advice on how to source practical support. Read more
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
All of the latest updates about Coronavirus vaccines and their impact on the AA community. Read more
Many other charities and organisations are available which can provide support to people affected by aplastic anaemia. Read more
If you were going to stay overnight in hospital, what three things would you want to pack to take with you? Read more
Regular online meet ups, for advice and emotional support. Connect and share your experiences of coping with Covid-19. Read more
Some helpful resources to support you and your child through the pandemic Read more
Our new informative webinar series to help you through the pandemic Read more
Aplastic means your bone marrow is failing to produce enough of ALL essential blood cells Read more
We are excited to be launching our brand new spring awareness campaign! Read more
The Peak District Walk in September 2019 was truly exceptional, with over 100 people enjoying each other's company, stunning scenery, lots of sun and gorgeous food, whilst raising awareness and funds for our the Aplastic Anaemia Trust! Read more
We have launched 3 brand new How to Guides to offer you advice on maintaining good oral health, managing a nose bleed and increased urinary urgency. Read more
Staff from Oldham Care Organisation benefit from specialist training on aplastic anaemia Read more
When you shop at over 4,300+ top stores including John Lewis & Partners, Expedia, Asos and others via Give as you Live, they'll turn a percentage of your spend into free funds for us! Read more
A £1.15m grant from LifeArc and The Aplastic Anaemia Trust will support researchers from King’s College London and King’s College Hospital to test a personalised treatment approach for Aplastic Anaemia patients who have not responded to available therapies Read more
After more than 40 years' involvement with the AAT, the much-loved Prof Ted Gordon-Smith decides now is the time to begin enjoying retirement but carries our flag as Patron Read more
We have joined the SHCA as a patient-focused organisation working in a rare disease area to improve our access to national policy updates and increase our ability to influence the UK's Rare Disease Strategy Read more
A key figure in UK’s haematology, Professor Ted Gordon-Smith, reflects on the evolution of the vital Blood Transfusion service in the UK. Read more
Thank you our crowd of supporters who risked the rain on Saturday 11 May 2019 and made our annual Windsor Great Park Walk a huge success Read more
Aplastic anaemia can acquired or inherited. It can be moderate, severe or very severe. Read more
Join our small and growing charity. Help us make a tangible positive difference to everyone affected by aplastic anaemia and allied rare bone marrow failures Read more