Martin’s MND fundraising

HOW LIFE CHANGES…

Martin was diagnosed with MND in October 2021, neither he nor his partner Graeme saw it coming. Up until January 2021, Martin and Graeme led a very active and vibrant life. They started their journey together in 2005, married in 2008, built a successful business and when the time was right, they adopted their son; their life was perfect! However, in early 2021 Martin’s speech be

gan to slur and after many visits to doctors a year of testing for various conditions and misdiagnoses, they were eventually given the heartbreaking news that he had MND. Martin’s variation of MND is ALS (Amyotrophic Lateral Sclerosis). After some investigation, Martins's MND was found to be carried genetically from his Uncle who had died from the illness some years before. Since his diagnosis, this perfect loving family unit has been on an emotional roller coaster as they navigate their way through all the information, endless consultations that all provide insight as to what is ahead. Martin has maintained the most incredible positive attitude throughout and is determined to do whatever he can to fight this illness. The progression of Martins's MND has been given a 3-5 year term but there are many cases where this time scale had doubled so by keeping as fit and healthy as he can Martin is giving himself his best chance. We want you all to follow Martin’s page so that we can share his story and raise much-needed funds for Motor Neuron Disease Association. Hopefully, it might also help others diagnosed with MND find their inner determination and positivity as they navigate their own MND roller-coaster.