Olly is 9 years old and he had open heart surgery at the Leeds Congenital Heart Unit this year.

On 4th February this year, Olly was admitted to hospital with breathing difficulties. He didn’t come home for 48 days.

Many of those days were spent in an induced coma, on a ventilator in Leeds Children’s Hospital PICU (Paediatric Intensive Care Unit) – Olly was suffering from heart failure.

Olly’s mum Helen told us a bit more about his condition…

“A defective mitral valve, likely congenital, meant Olly needed open heart surgery to fit a mechanical replacement valve. The surgeon in Leeds performed this procedure just under a month after Olly was admitted, on 1st March.

 

“Following his operation Olly’s condition improved. However, the 3 weeks spent in PICU before surgery meant his muscle mass was significantly depleted and he had become dependent on the sedatives required when he was ventilated.

 

“This meant a long weaning plan and lengthy rehabilitation post-surgery.

 

“Having always been an active child that showed no signs of any issues, the speed at which Olly deteriorated was a huge shock to us all.”

Olly’s mum, dad and brother Robert stayed in CHSF-funded accommodation at the hospital. Having family so close by for the 48 days he was in hospital really help Olly to recover.

During this time, Olly’s mum, dad and brother Robert were able to stay in CHSF-funded family accommodation as they live nearly an hour away from Leeds. This meant Olly had his whole family close by while he recovered in hospital.

Olly is now home and as well as completing his own fundraiser for CHSF earlier this year (just four months after his surgery!), he has also been helping us to promote our Christmas Campaign for 2023, ‘Stay Another Day.

Olly writes:

Hello I’m Olly and I’m 9.

 

I was in hospital in Leeds for 48 days with heart failure this year, I needed to have heart surgery, which was scary for me.

 

We live in Addingham, which is nearly an hour from Leeds. My mummy and daddy were able to be near me because they could stay in Leeds. The room they got even meant my brother, Robert, could stay too. Seeing them all the time really helped me get better.

Since I got home, I have raised money to give back to charity to thank them for their help. Please can you give money to charity this Christmas? They can make sure other mummies and daddies are near their poorly children when they need them most.

 

Thank you, Olly
P.S. Merry Christmas!

Since our charity was founded in 1988, around 10,000 families have stayed in CHSF-funded accommodation at the hospital.

13 babies are diagnosed with congenital heart disease in the UK every day. This year alone we have supported double the families that we did in 2022.

We need to raise at least £10,000 every year to fund CHSF accommodation.

Please donate what you can to help us reach our goal and ensure heart families just like Olly’s can #StayAnotherDay.

If you can go the extra mile (so heart parents don’t have to), please consider setting up a regular gift to CHSF to enable more families to #StayAnotherDay throughout the year!

Set up a direct debit to CHSF…

CELEBRATE CHRISTMAS WITH CHSF

Have a festive flutter on the 2023 Christmas Raffle, or maybe you could buy a pack of Xmas cards. Want a challenge? You can Step Into Christmas by walking a marathon in December, or Jingle All the Way to 5K with Team CHSF!

The most wonderful time of the year is almost upon us again. Can you help us be there for heart warriors all year round?

Visit our Christmas page to see more ways you can support CHSF this festive season!

Carin van Doorn to receive OBE in King’s Birthday Honours

Carin van Doorn to receive OBE in King’s Birthday Honours

Ms Carin van Doorn (Consultant Congenital Cardiac Surgeon at Leeds Children’s Hospital and CHSF Charity Trustee) has been awarded Order of the British Empire (OBE) in the King’s Birthday Honours list. Carin is recognised for her enormous contribution to children’s...

CHSF donates £15,000 to Eckersley House

CHSF donates £15,000 to Eckersley House

Children’s Heart Surgery Fund (CHSF) have awarded a further grant of £15,000 towards Eckersley House, a ‘Home from Home’ run by The Sick Children’s Trust for parents with a seriously ill child in hospital. Since being relocated next to the Leeds Children’s Hospital in...

#TeamCHSF Dragon Boat Challenge 2025

#TeamCHSF Dragon Boat Challenge 2025

On Saturday 12th July, the CHSF team will be competing in a Dragon Boat Race - and we'd love your support! Organised by the Rotary Club of Wakefield Chantry and Normanton, it’s a fun day for the whole family. #TeamCHSF will complete against 40 teams from local...

Support for families: May 2025

Support for families: May 2025

"This month we have reflected on connections. We tend to focus on positive outcomes in terms of a successful surgery, a family going home after a long admission or the speedy recovery of a patient - but we sometimes forget those small wins and bonds formed through CHD...

Bonnie

Bonnie

Bonnie is two years old and was born with Atrial septal defect (ASD) and Ventricular septal defect (VSD) which were surgically repaired in Leeds at age 4 months. She has just celebrated her second heart day on 4th May! Mum Charleigh tells us about Bonnie's CHD journey...

Running for Ruben – Laurie’s 5th Great North Run

Running for Ruben – Laurie’s 5th Great North Run

Heart hero Ruben was born in 2019 with coarctation of the aorta. He had open heart surgery at just 3 days old, but mum Laurie Higgins says he is now a ‘happy and healthy’ 6 year old thanks to the Leeds Congenital Heart Unit team. Laurie tells us why she has chosen to...