Opportunity
Chair of Trustees

Help empower the lives of everyone born with congenital heart disease (CHD) in our region.

Children’s Heart Surgery Fund (CHSF) is a unique life-changing service driven and inspired by CHD patients in our region, working to enable affected children, adults and families to live their best lives.

As recently as 50 years ago, most children born with CHD died very young. Thanks to advances in treatment both locally and globally there are now more adults than children living with CHD and 90%+ infants survive to adulthood. Fundraising through businesses, individuals and trusts, CHSF provides life-saving medical equipment and a suite of services including family support, hospital accommodation and more, serving Yorkshire and Humber, North and North East Lincolnshire and North Derbyshire.

We are looking for our next Chair to drive CHSF’s mission and objectives, providing inclusive leadership and ensuring that colleagues collectively deliver on their duties and responsibilities for effective charity governance. 

Location/time commitment: Leeds in-person meetings quarterly, with two strategy sessions per year. Subcommittee meetings are virtual. Approximately 1 day a month.

Salary: Unremunerated, all reasonable expenses covered.

Closing date: Monday 27 April 2026, 5pm
Interviews: 7-8 May 2026

For any more information, including informal contact with the Chair/Deputy Chair/CEO which is also available to potential candidates, contact ruth.davany@chsf.org.uk.

LATEST NEWS

Wakefield heart hero set to conquer Great North Run for CHSF

Wakefield heart hero set to conquer Great North Run for CHSF

21-year-old Danny Hirst was born with a hole in his heart, which was discovered when he was just 6 weeks old. Danny had open heart surgery in Leeds when he was 11. And he is set to take on the Great North Run to raise vital funds for the charity which helped him and...

Be a hero for…LOCHIE!

Be a hero for…LOCHIE!

Lochie Blue is 2 years old and lives in Silsden near Keighley. He was diagnosed at 10 days old with Coarctation of the aorta, Ventricular septal defect (VSD) and Atrial septal defect (ASD). Lochie and his family will be at this year's Superhero Walk and we spoke to...

Fundraiser of the Month: Family & Friends of Isaac Phoenix Davison

Fundraiser of the Month: Family & Friends of Isaac Phoenix Davison

Isaac was born in November 2022 with a heart condition called Tetralogy of fallot. Mum Leanne, tells us a bit more about her son and the fundraising family and friends have been doing in his memory since Isaac sadly passed away in April last year.Leanne said: “Isaac...