This is a fundraising page im doing to help raise money for people like my cousins little one aurora who suffers daily with this condition, i honestly take my hat off to my cousin who has her own business and a poorly little girl yet still goes along day to day life as normal.

Aurora is sooo brave and puts a smile on every one’s face she meets, she has had numerous hospital stays and yet still smiling, my cousin and her partner are so strong and an inspiration to any parents.

I had never heard of this condition untill aurora was born, it’s not a condition that is heard of a lot but it is one that has no cure.

E40 wars at nottinghams QMC have been amazing with both jade, her partner and aurora and this amazing little one wouldn’t be here with out there help and support.

Thank you for reading this and taking the time to donate.

Harry's Hydrocephalus Awareness Trust (Harry's HAT) was founded in 2018, the charity is user-led. The aim of the charity is to make life better for children with hydrocephalus and their families.

Every year 1 in 770 babies will develop hydrocephalus, there is no cure and it is currently the most common reason for brain surgery in children. The charity exists to raise awareness, promote training and so improve patient care, support families to reduce isolation and to campaign for better awareness of infant head circumference measurement.