Our beautiful baby boy, Noah, was born with a disease called Langerhans Cell Histiocytosis (LCH). It's so rare, 1 in 2,000,000 are thought to be born with it. Unfortunately, our precious boy fell into this category.

Although Noah is doing amazingly well, surprising us and his oncologist every day, a relapse for a patient with LCH is common.

Therefore, our aim is to raise as much awareness and funding as possible towards better treatments and finding a cure for his disease.

As part of this journey, me and my sister-in-law, Laura, will be abseiling down the Liverpool Cathedral on 18th August 2018.

Please help and support us if you can, every penny helps, and every share spreads awareness!

Thank you 💙 xxx