Hi, I'm Hannah, and I'm here to help you fundraise!
Whether you'd like a collection box, a place at a running event, or just someone to talk your ideas through - that's what I'm here for.
Whether you're fundraising as a thank you to our team, in memory of a loved one, or to support someone who's recently been diagnosed - everyone's needs are different. So do get in touch for a chat - I'd love to hear from you.
This year, The Aplastic Anaemia Trust are raising money to fund our support and information services, create new nurses' training to help healthcare professionals to care for rare bone marrow failure patients, and fund the TIARA trial at Kings - trialling a brand new Treg treatment for aplastic anaemia. You can make these things happen!
Email me at [email protected] or call 07849691356.
Start your own fund, with your own fundraisers and brand. Including Future of AA Research Funds, designed to fund the next big leap forward in treatment.
Work with us to celebrate the life of a loved one. From funeral donations and in memory pages, to special events and challenges.
We'll design bespoke wedding favours for your big day
Celebrate the anniversary of your bone marrow transplant
Join our annual Rare Disease Day campaign and earn this year's tee!
How will you raise awareness on 8th March?
Get ready for Christmas with a cold water dip!
Double (or quadruple!) your fundraising or donations.
If you're not in a position to fundraise or donate at the moment, there are other ways you can support The AAT and aplastic anaemia patients...
Check out the campaign page for the latest actions you can take to help campaign for equal access to this new medication across the UK
Support the campaign
We won't stop asking for aplastic anaemia to be added to England's NHS website. You can help by signing the petition and writing to your MP
Join in
We're always looking for volunteers - from cheer point cheerers to Facebook group moderators! Email [email protected] or check the boxes for volunteering options when you register.
Volunteer
Filling in our registration for only takes a few minutes, but providing us with that data makes a huge difference in our ability to report on the numbers of patients, friends and families we're reaching in the UK.
Fill in the form
Catch up on the latest news from projects funded by your fundraising
We've moved some things around... Read more
Yesterday, Ellie from The Aplastic Anaemia Trust was invited to the NHS Blood Donation London West End Donor Centre, to talk at their training day. The absolute highlight was this gorgeous video which Terri (from Jensen's Story) created specially. Read more
Erica and Aimee pack up a Bravery Box. But what's inside? Read more
The Aplastic Anaemia Trust, our Research and Clinical Advisory Panel, and Professor Ted Gordon Smith have published a report into the priorities for research and improving clinical care in rare bone marrow failure. Read more
For over 40 years, we’ve been working to change the story for people affected by aplastic anaemia. And the progress we’ve made - from life-saving research to vital patient support - has only been possible because of those who came before us, and those who have chosen to leave something behind. We're recently launched a free Will writing service, we’re asking: What will your legacy be? Read more
The last video in our little series: Given all these improvements, what should we be looking forward to in the next 40 years? Professor Gordon Smith and Dr Austin share what they're most excited about. Read more
We learn about why The AAT started, who started it, and what that had to do with tents. Read more
The NHS website for Scotland publishes three pages of expert content about aplastic anaemia. Read more
Sam Williams from The Aplastic Anaemia Trust Support Team is the TIARA trial’s Patient Representative. He explains why his own experience of treatment side effects and his conversations with patients mean he's excited for this potential brand new treatment. Read more
King’s College Hospital and King’s College London are trialling cutting-edge cell therapy to develop a brand new treatment for the condition. It’s a world first - funded by The Aplastic Anaemia Trust and LifeArc. On 7th December, Dr Nazia Matto, the trial’s lead GMP production scientist presented initial findings from the TIARA trial, revealing promising results Read more
Barbara had been in hospital in isolation, but on the first day she was allowed to leave the room - she walked out of the building, across the road to the Maggie's centre and found Zoe. Read more
Families had a fab time on our London Wildlife walk - with huge thanks to London Wildlife Trust for welcoming us to Walthamstow Wetlands. Read more
The Aplastic Anaemia Trust will fund a new research project, investigating genetic mutations in patients with aplastic anaemia or PNH. Read more
We are very proud to announce that the recent Leeds Covid vaccination study, funded by The Aplastic Anaemia Trust, has been published today in The Lancet Haematology. Read more