OUR STORY

The Matt Gallagher Foundation was formed after former rugby player, Matt, was diagnosed with Motor Neurone Disease in October 2023. Despite this incredibly unexpected and abrupt diagnosis, one of his first thoughts was that he wanted to help others in his situation.

OUR STORY

The Matt Gallagher Foundation was formed after former rugby player, Matt, was diagnosed with Motor Neurone Disease in October 2023. Despite this incredibly unexpected and abrupt diagnosis, one of his first thoughts was that he wanted to help others in his situation.

BACKGROUND AND OUR FOUNDER

After falling from a ladder in June 2023 and undergoing surgery to repair the resulting injury to his arm, Matt experienced some unusual symptoms and was referred for tests. After months of back and forth, during which time Matt’s eldest daughter, Hollie-Mae, graduated from university, Matt and his son Jack toured with Solihull School to South Africa and the family holidayed in America, Matt and his wife, Lisa, went back to the hospital to receive his results. Matt was diagnosed with Motor Neurone Disease on 14th October 2023,  news which left the couple reeling and feeling extremely overwhelmed. 

Despite this incredibly unexpected and abrupt diagnosis, one of Matt’s first thoughts was that he wanted to help others in his situation, especially after learning that there were just three specialist MND nurses serving the West Midlands, one of the largest health authorities in the UK. And so, the Matt Gallagher Foundation was born, a community designed to support those living with MND and their families.

As a former professional rugby player, Matt has made a significant impact on the sporting world over the years. Having started playing for Solihull Rugby Club at the age of five, he was playing for The Birmingham Bees’ first team by the age of 18, before continuing his career with his Polytechnic team at Sheffield Hallam (where he won the British Polytechnic Cup twice) and Nottingham Rugby Club, playing in the Championship at the age of 20. He then signed for Coventry RFC in 1996, playing more than 100 games for the team before leaving in 2001. Matt concluded his rugby career back at Birmingham and Solihull, where it all started, and retired in 2003, switching his focus to raising his three young children and building a new legacy in the housebuilding industry. 

Although he no longer plays professionally, his passion and commitment to the sport mean that he still has a heavy involvement in the industry, coaching his son’s school team and running the former players’ association for Coventry. 

Before he retired from rugby, Matt started a successful career in the housebuilding industry and now runs his own business, further adding to his extensive network. It’s this network that makes the Matt Gallagher Foundation so special, not only providing a strong support system, but also allowing him to harness his wide range of connections to help others living with MND.

OUR MISSION

We are not a research-led charity, we aim to make a direct, positive impact on those living with MND today, by offering fast support and a large network of contacts who can help in many different ways.

 Whether it’s funding a mobility vehicle, sourcing and installing a stairlift, or helping to fulfill a dream family holiday to make lasting memories with loved ones, we understand that time is of the essence and the delays in support often provided by larger organisations can cause additional pain and suffering for those already going through tough times. 

Motor Neurone Disease is rare, meaning that the number of specialists in the UK is limited. One of our main fundraising aims is to provide an additional permanent specialist NHS nurse for the West Midlands, meaning that support across the region will be more accessible and frequent. Our mission is to make sure that every person who receives an MND diagnosis has the support they need to maintain hope and positivity throughout their journey. It’s Matt’s infectious optimism that has inspired the foundation and we want to spread that throughout our community by giving those living with MND the resources and funding they need to keep living happy, fulfilled and dignified lives.

We are striving to beat MND and the impact it has on people across the UK. We aim to raise money, raise awareness and have a good time along the way!

OUR VALUES

Our Values - We act quickly

We don’t leave anyone behind

We don’t leave anyone behind - The Matt Gallagher Foundation is built to support anyone affected by MND, without question.
Our Values - We don’t leave anyone behind

We act quickly

We understand that time is precious and when we offer to help, we make sure it’s done in the fastest, most effective and sensitive way possible.

We get busy living

Our ethos is focused on allowing those living with MND to continue to enjoy life, reducing unnecessary stress wherever we can.

We are optimistic

We live in hope that a cure will be found and empower our community to stay positive.
Our Values - We get busy living

We connect people

We are privileged to have a strong network of contacts and friends and are committed to harnessing this to help others.

We support each other

We know that it’s a challenge to stay positive when times are tough, but we are always here to support our MND community.

We have fun

We love seeing our supporters take part in our events and run incredible fundraisers, having a good time whilst contributing to such a great cause.

OUR PEOPLE

TRUSTEE

Matt Gallagher

TRUSTEE

Lisa Gallagher

TRUSTEE

Andy Foote

TRUSTEE

Charlotte Jones

Charity MANAGER

Hollie-mae Gallagher

NEWS & EVENTS