Hannah's Fund News

ACCORD project - sharing stories

On March 4th 2023 Headlines Craniofacial Support launched a series of films made by and for adults living with Craniosynostosis. The...

Sally and the ACCORD project

Following on from my article posted on this website in 2022 about my journey of living with Crouzons Syndrome, I thought I would share my...

Join in with The Great Bristol Run

On May 14th this year we have a small determined group who have signed up for The Great Bristol Run and would would love more people to...

60 Things for Hannah's Fund

In 2023, the year she turns 60 one of our Trustees, Punch Maughan, is setting herself a challenge of achieving 60 new, different or...

Literary Laughs 2022

On the 7th December 2022 Hannah’s Fund held a ‘Literary Laughs’ Quiz Night. A national initiative which encourages Book Clubs to come...

Family Fest is Great Success in 2022

The inaugural Hannah’s Fund Family Festival in 2022 was a great success. We were very grateful to St Stephens C P School - Saltash for...

Sally's Story - Living with Crouzons

I was born in the 1960s and was diagnosed with Crouzon’s Syndrome when I was two-years old. In those days knowledge of craniofacial...

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