My son was diagnosed with severe AA two years ago therefore the work you do is important to me. Read more
As a 22-year-old it never did dawn on me that I could get ill long term. Read more
To support awareness, due to my sister being diagnosed with aplastic anaemia her self. Read more
Raising funds and awareness for The AAT ahead of Rare Disease Day Feb 28th 2021 Read more
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
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I like to support rare diseases and small causes so that they can get some awareness! Read more
I am a post transplant patient Read more
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
Join our team for the Oxford half marathon! Read more
How does it feel to get a disease you’ve never heard of? Read more
Dagmara joined the AAT in 2018 to build a Trusts & Foundations income stream. In 2020 her role evolved to include impact management. Read more
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
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
For the help and support from The Aplastic Anaemia Trust since diagnosis Read more
I am so proud to be the CEO of this incredible charity, supporting people impacted by such a serious and rare disease. Read more
Social media graphics for you to use to support your Super Rare fundraising. Read more
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
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
Set yourself a challenge to complete in February 2021 and raise money and awareness for aplastic anaemia. Raise £150 before Rare Disease Day and earn your limited edition Super Rare T-shirt! Read more
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
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
Sam was recruited part-time in 2020 to support patients on our helpline and online. Read more