Dean Fox MND Foundation

The Dean Fox MND Foundation was established by Dean and Christine Fox following Dean’s diagnosis of Motor Neurone Disease (MND), also known as ALS, in August 2023.

Dean, from Middlesbrough, was a devoted husband to Christine, a proud father to two sons, a cherished father-in-law, a loving grandfather to two grandsons, and a doting owner of two much-loved grand dogs. He was also a mentor, coach, and friend to countless people whose lives were positively impacted by his passion for helping others achieve their goals and realise their potential.

In May 2023, Dean was diagnosed with cancer. A few months later, after almost a year of symptoms, he received the devastating diagnosis of MND. Despite facing two life-changing illnesses, Dean approached every day with extraordinary courage, determination, and positivity. Drawing upon the mindset principles he had spent more than 13 years teaching others, he focused on living life to the fullest, inspiring those around him, and making the most of every moment with family and friends.

On 15 December 2024, Dean sadly lost his brave battle with MND.

While Dean is no longer with us, his legacy continues through the Foundation he helped create. His unwavering belief in resilience, kindness, and supporting others remains at the heart of everything we do.

Motor Neurone Disease is a progressive neurological condition that affects the brain and nerves responsible for controlling voluntary muscles. It has no cure, and its impact on individuals and families is devastating. The need for research, support, and awareness has never been greater.

Today, the Dean Fox MND Foundation continues its mission to honour Dean’s memory by:

• Raising vital funds to support research into MND and the search for effective treatments and ultimately a cure.

• Providing financial assistance to local MND support groups and organisations that offer invaluable help to individuals and families affected by the disease.

• Offering grants and practical support to people living with MND, helping them create precious memories and spend valuable time with their loved ones.

• Raising awareness of MND and the challenges faced by those living with the condition.

Dean understood better than most how precious time with family and friends truly is.

Through the Foundation, his family hopes to ensure that others facing similar challenges receive the support, care, and opportunities to make lasting memories together.

Every donation, fundraiser, partnership, and act of support helps us continue Dean’s vision and make a meaningful difference to the lives of those affected by MND.

Thank you for helping us honour Dean’s legacy and bring hope to families facing this devastating disease.

If you would like to support the Foundation or find out more about our work, please contact us through the website or email us at info@deanfoxmndfoundation.org.

Together, we can continue Dean’s fight against MND.

Dean Fox MND Foundation