Providing support and information to the UK anorectal malformation community.
What we do
Max’s Trust provides support and information to adults, children and families who are affected by anorectal malformations in the UK. We also fundraise, hold events and conferences and take part in research projects.
Max Finnigan
Max was born with an anorectal malformation in 2017. His sudden death when he was 17 months old inspired the creation of the UK’s first anorectal malformation charity, by his parents and others affected by ARM.
A.R.M
Anorectal malformations are a group of malformations where the anus and rectum don’t develop properly. It is a congenital condition occurring in early pregnancy while the baby is developing and affects 1 in 4,000 to 5,000 births.
News
Find all the latest news research and developments from Max’s Trust and the anorectal malformation community.
Fundraising
Support Max’s Trust by holding your own fundraiser with family, friends and colleagues, or by making a donation.
Events
Find out about all the events that we take part in and host, including our popular annual conference
Research
We support research projects aimed at improving the lives of those affected by anorectal malformations.
Support
As well as providing support, we collaborate with other organisations both in the UK and Internationally.
Trustees
Our trustees work hard to improve the lives of the ARM community - meet the team behind the scenes at Max’s Trust.
Because of our Trustees we are doing more good for more people!
Lauren.
Andy
Helen
Hattie
our Founders
Our Founders Jon and Cassie.
About Max
On the last day of a very hot June 2017 Max Freddie Finnigan arrived, bang on time, at the John Radcliffe Hospital, Oxford. All 10 gorgeous pounds of him!
