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!
Freddie
Last year, Freddie was the first child in the UK to undergo the innovative Yasui repair instead of the Fontan. Freddie was born with Hypoplastic Left Heart Syndrome and a large VSD and since 2016 had already overcome multiple heart surgeries. Mum Casey shares...
Sally
Sally's heart defect wasn't identified until after she was born and had open heart surgery at 18 days to correct her CHD. Doctors at the Leeds Congenital Heart Unit stated that without this operation, Sally wouldn't live past 6 months old. Now 21, Sally has already...
Jacob
Born at home in Kippax Leeds, Jacob's heart defect was detected in his first week of life after being admitted to Leeds Children's Hospital when he wasn't feeding well...Jacob's mum, Iona, said: "Jacob was born at home; everything was amazing and there was no sign...
Daisy
Daisy's mum, Lucinda, said: "Our experience with congenital heart disease began at our 20 week scan. Having previously had a history of problems, we were told that baby would be checked very carefully. Upon her silence we immediately knew the sonographer had found...
Rebecca
Although Rebecca was born with the heart murmur, it wasn't until she was pregnant with her second child that her heart problems became more apparent...Rebecca said: "From birth I have had a heart condition. I was born with a heart murmur and was under the care of...
Welcoming Cardiac Speech and Language Therapist Jess
Thanks to a generous donation from our corporate partner Caddick Group, The Hospital Saturday Fund and additional funds from our wonderful supporters, CHSF has been able to fund a dedicated Cardiac Speech and Language Therapist – Jess Symonds - who has just started in...





