Team Jude
Our son Jude was born in 2017 with early-onset mitochondrial disease – a rare and devastating condition that affects every part of his body. It means his cells can’t make the energy they need to function. Because of this, Jude cannot move, walk or talk, and he relies completely on us for all his care.
Yet even without words or movement, Jude speaks to us in his own remarkable ways. His eyes light up a room, his smiles melt hearts, and his quiet presence brings calm and love wherever he is. He teaches us every single day what courage, strength and unconditional love truly mean.
Life with mitochondrial disease is incredibly hard at times – hospital stays, sleepless nights and constant uncertainty. But it’s also filled with love, laughter and moments of pure joy. Jude’s twin brothers, Rocco and Ryleigh (aged 10), and his big sister, Correy Ellen (aged 12), adore him. They sing to him, make him laugh and bring sunshine into even the toughest days. Watching the bond between them is something we’ll cherish forever.
The Lily Foundation has been a lifeline – helping us understand Jude’s condition, connecting us with other families and giving us hope that one day, there will be answers.
Jude’s life has changed ours forever. He has shown us what truly matters – love, resilience and the strength of family.
How to support Team Jude
Jude’s family would love you to support The Lily Foundation’s work. Whether it’s a one-off gift or a regular contribution, simply follow the link below to visit their JustGiving page and join the hundreds of others who have already made a difference.
Your donation will help fund groundbreaking research into mitochondrial disease, raise vital awareness and support hundreds of patients and families affected by this little-known but incurable condition.
Since 2007, The Lily Foundation have already raised over £11 million. With your help, we can continue to fight mito and find hope for everyone affected.
