Alanah was diagnosed with leigh's syndrome, a type of mitochondrial disease in December 2023. Sadly she lost her fight with the disease at just 15 months old on the 20th June 2024.

She was a beautiful bright happy baby girl, with a smile that would light up the room. She had so much love and happiness that she gave to everyone she met. No obstacle got in her way and she was brave and fought Mito till the very end.

The hole that her passing has left in the hearts of her family will never be replaced. Because of this, I want to make a difference in her memory.

There is no cure for Mito and it has taken to many lives. I am supporting The Lily Foundation, a charity dedicated to funding research to find a cure and support all those effected.

Please donate if you can and together we can give hope

Thank you