Team Ray
Born on 24th May 1995, our daughter Tirion was full of life, personality and a spark that was impossible to ignore. She had a wonderfully sassy sense of humour and a quick wit that kept everyone around her on their toes. She never hesitated to say exactly what she thought, often with a perfectly timed sarcastic remark or mischievous grin. Yet somehow, despite that sassiness, everyone who met her warmed to her almost instantly. There was something about her energy, honesty and humour that drew people in.
In 2013 she was diagnosed with mitochondrial disease, something that changed the course of her life and brought many challenges. But even through the hardest moments, she never lost the humour and spirit that made her who she was. In fact, during the darkest days it was often her jokes and cheeky comments that lifted the people around her. When things felt heavy or frightening, she would find a way to make someone laugh.
Her sass wasn’t just part of her personality – it was part of her strength. She refused to let illness define her or take away the vibrant, funny person she’d always been. Doctors, nurses, friends and family all remember her humour and the way she could brighten even the toughest moments.
She passed away in April 2018, but the impact of who she was has never faded. Her courage, humour and bold spirit remain part of the memories she left with everyone who knew her.
How to support Team Ray
Tirion’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.
