Acutely aware of being incredibly rare

Andrea's rare

Daisy's rare

Jane's rare

Laura's rare

Lisa's rare

Mandy's rare

Michelle's rare

Natalie's rare

Nick's rare

Ros's rare

Stephen's rare

Latest

Daisy's Running March

I have had AA and PNH for 12 years now, and have had so much support from the charity that it's always important to me to give back when I can.
Broadstairs Bathers Daily March dip

To help raise vital funds to support research into Aplastic Anemia
The AAT funds new research into COVID-19 vaccination responses in patients with aplastic anaemia and PNH

The new study will shed light on the question of how effective the Covid-19 vaccines are in aplastic anaemia patients.
A dad's tale: What it's like when your one year old son is diagnosed with an ultra rare disease

For Rare Disease Day 2021, Connor reflects on his experiences as dad to one year old Max, who is in treatment for aplastic anaemia.

Most read

Jerome: my aplastic anaemia story so far

My journey from diagnosis to transplant
What is aplastic anaemia?

Aplastic means your bone marrow is failing to produce enough of ALL essential blood cells
Buffy's story

This blog has been extremely hard for me to write...
James: life after an AA diagnosis

After being diagnosed aged 15, I had a tough ride with aplastic anaemia, but I lived to tell the tale.
Grace's adventure

Little did we know what was coming the next day in May 2017!
Tasha's story

Read the inspiring story of Tasha Townsend, our Olympic rower, who kicked aplastic anaemia's butt!
Alice: Life after childhood AA

Thanks to Alice and her family, the British Bone Marrow Register gained huge profile in the UK
Diagnosis and treatment

Diagnosis and treatment information for adult patients. It worth noting that some of the main treatment options may also apply to young patients, however they will be treated by experts specialising in paediatric aplastic anaemia.
Coronavirus shielding guidance and support

The latest updated guidance on shielding and advice on how to source practical support.
Our vision and mission

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

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Aplastic Anaemia Awareness Day ATG children diagnosis fertility fundraising Kids mental health Parents PNH post-transplant pregnancy research stem cell transplant Super Rare young people

Tasha's story

Read the inspiring story of Tasha Townsend, our Olympic rower, who kicked aplastic anaemia's butt! Read more

Macy's story

The touching story of Macy who survived aplastic anaemia Read more

Rikki: my rollercoaster experience of aplastic anaemia

Nothing can quite prepare you for the emotional and physical rollercoaster that is aplastic anaemia. There’s no best-selling book that can teach you how to deal with the turmoil of an illness that wasn’t there yesterday but is very much there today... Read more

Investing in support for aplastic anaemia patients

We're investing in our team, to make sure every aplastic anaemia patient is supported. Read more