Meet Oliver from Hull who was born with a heart condition called Tetralogy of fallot.

Thanks to the life-saving work of the Leeds Congenital Heart Unit, Oliver is thriving and has been able to pursue art as a hobby and, more recently, a career in finance!

Now 22, Oliver shares his journey with CHD so far and how he has supported CHSF with his family to say ‘thank you’ for the care he received in Leeds…

“I was born with Tetralogy of fallot and had open heart surgery when I was a year old.

 

“When I was sixteen, I had my second open heart surgery to replace one of my valves and I now have an annual heart scan to check how my heart is doing.

 

“Throughout my life, my family have done many casino nights and coffee mornings to raise money for Children’s Heart Surgery Fund.

Oliver had his first open heart surgery at Leeds wheen he was just a year old.

Oliver and his brother share a passion for art so arranged a fundraiser for CHSF where they raffled off a drawing commision as part of a Coffee Morning,

“In 2022, I worked with my brother to arrange our own fundraising coffee morning, which was a great success. As part of our coffee morning, we held a raffle for a drawing commission done by me and my brother, since we are both passionate about art.

  

“I started at Arco in 2021 as a finance apprentice, and I passed my level 2 AAT Foundation certificate in accounting apprenticeship at the start of 2023. Most recently, I started the level 3 qualification of AAT in September of 2023.

 

“My apprenticeship and job have greatly helped develop my confidence and I enjoy the range of tasks that I do within the Transaction Team of Arco’s Finance department.”

We’re really grateful to Oliver for sharing his story with us. It is so inspiring for young heart patients and families to see a young adult doing so well.

We are of course also so thankful to Oliver and his family for their continued support of CHSF!

Inflatable 5K for Mabel

Inflatable 5K for Mabel

Leah and Brad found out the 20 week scan that their daughter, Mabel, had Coarctation of the aorta, a large Ventricular septal defect (VSD) and a smaller left side of the heart. She had open heart surgery at five days old. Now Mabel's family are taking on the Leeds...

Support for families: May 2026

Support for families: May 2026

"The support was amazing and the team got me through the hardest time of my life. Amazing support" -- heart mumDuring the month of May... 39 families worked with overall 23 families received a tailored packaged of Family Support 8 families engaged with -- 6 young...

Ruth’s Round-up | June 2026

Ruth’s Round-up | June 2026

As we head into a busy summer for Children’s Heart Surgery Fund, it’s a great moment to reflect on the incredible connections we’ve been building - and the exciting opportunities ahead. Recently, I had the privilege of attending the Somerville Heart Foundation’s...

Kalina’s Heart Day

Kalina’s Heart Day

Because of the incredible work of the Leeds Congenital Heart Unit and because of your support, Kalina celebrated her first heartiversary on 3rd June this year. Happy Heart Day Kalina from all of us at Children's Heart Surgery Fund!Kalina's mum Karly-Kay said: "It’s...

100km for Matilda

100km for Matilda

Heart mum Danielle shares her experience of daughter Matilda’s heart condition – from diagnosis at 20 weeks to the time they spent at Leeds General Infirmary and once home. She’s now taking on a 100km Ultra Challenge to give something back to CHSF after the support...

Support for families: April 2026

Support for families: April 2026

"Thank u for remembering me. I can imagine u meet lots of families"-- heart mum, during a 'touching base' callDuring the month of April... 63 families worked with overall 25 families received a tailored packaged of Family Support 38 families engaged with -- 16 young...