Arthur was born via C-section in March 2011 after a complicated pregnancy. Despite a few blood sugar issues and mild jaundice, he was otherwise healthy.

At six months old, his blood showed an abnormally raised lactate, prompting us to investigate further. After a series of tests, including brain scans, muscle biopsy, skin biopsy and heart scans, Arthur was diagnosed with mitochondrial disease, aged eight months. This devastating diagnosis left us struggling to cope with medical appointments and treatments. We know we were lucky to receive such a quick diagnosis.

We reached out to Liz, an incredible advocate from The Lily Foundation. The foundation has provided invaluable support and friendship to us and our family. It’s a remarkable charity that makes a tangible difference to those affected by mitochondrial disease.

Arthur is doing well and we’ve had great support from people offering to raise funds in his name. He loves football, food, parties, games, music and making people laugh. He’s a great character who makes an impact on everyone he meets.