Ultimate Quiz

My son was diagnosed with severe AA two years ago therefore the work you do is important to me. Read more

Starting the Journey

As a 22-year-old it never did dawn on me that I could get ill long term. Read more

Rareing To Go

To support awareness, due to my sister being diagnosed with aplastic anaemia her self. Read more

Super Rare 2021

I got diagnosed with Aplastic Anaemia in 2015 - I had never heard of it... which almost made it more scary. I would like to make it more well known :) Read more

Running for Tash

I like to support rare diseases and small causes so that they can get some awareness! Read more

Kainan Walk

I am a post transplant patient Read more

Chemistry Bingo Coffee Morning

The AAT has been a huge support to my son Ryan and my family with information since his initial diagnosis of AA in 2018. The online support events have been a great emotional support to me during lockdown and I want to give something back to the trust. 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

Lauren's Walk

To raise awareness of aplastic anaemia and to raise funds for the charity who provide support to people with this condition and their families Read more

Ros’s challenge

For the help and support from The Aplastic Anaemia Trust since diagnosis Read more

28 days of Getting in the Freezing Sea

I am so proud to be the CEO of this incredible charity, supporting people impacted by such a serious and rare disease. Read more

Super Rare social media

Social media graphics for you to use to support your Super Rare fundraising. Read more

We're hiring! Apply to be our Supporter Experience Assistant

Do you get a kick out of someone else’s joy as they reach their fundraising target? Are you an excellent communicator online and on the phone? You could be our next Supporter Experience Assistant... Read more

Super Rare 2021 - tea and biscuits

Post your pals some Super Rare biscuits and meet up online for a cup of tea and a chat - help us to spread the word about aplastic anaemia and raise funds to support people with this super rare disease. Read more

Super Rare 2021

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