“Without Children’s Heart Surgery Fund, Reggie wouldn’t be here.”

Michelle, Reggie’s mum

Written by Reggie’s mum, Michelle

Reggie was born on the 1st September 2016 with a palliative congenital heart disease called hypoplastic left heart syndrome. Although you might not know to look at him, Reggie’s heart is extremely poorly.

 

When we had his diagnosis at 20 weeks, we were given three options: abortion, comfort care or surgery. We chose surgery as we needed to let him have that chance.

 

Congenital heart disease is the biggest childhood killer, and Reggie is high risk for things like stroke, cardiac arrest, endocarditis…

Although we knew the possible outcomes, we still wanted to let him have the chance. We say that it’s his fight. When he’s tired, that’s his choice to stop! We will guide him as much as we can.

 

At four days old, Reggie needed his first open heart surgery. The operation was nine hours long. After three days, he needed to go back to theatre and be opened up again due to an infection. He came home in October, just in time for his mummy’s birthday.

In March the following year, Reggie needed another open heart surgery. He was so strong, but he had a really tough time with another infection, this time in his PICC line. We were home after eight days.

 

It hurts every day knowing that this CHD could just randomly take him unexpectedly or that when he needs a transplant, will he manage to hold on?

 

Imagine waking every day knowing it could be your child’s last.

Now age 6, Reggie is waiting for his final surgery.

 

He’s been on the list for the last year, but we haven’t had the call just yet with COVID and new babies being born with CHD that have taken priority.

 

Children’s Heart Surgery Fund are amazing. If you could donate this Wear Red Day, even if it’s £1, it will go towards saving a child like Reggie. Thank you.

Please register to take part in Wear Red Day this year, so you can help us raise vital fund and awareness to support children like Reggie. Thank you.

Louie

Louie

Louie's heart condition was detected at mum, Rebekkah's, 20 week scan. Louie would need life-saving surgery at Leeds after he was born and CHSF were there to ease the family's experience, providing vital assistance and comfort throughout Louie's treatment and...

Ebony

Ebony

When Ebony was born in September 2023, her congenital heart defect went undetected until she started to get very poorly at just over a week old. Ebony was 'blue-lighted' from Scunthorpe to Leeds, where she had emergency heart surgery to save her life...Ebony's mum,...

Wear Red like Barnburgh Primary

Wear Red like Barnburgh Primary

"In February 2023, Barnburgh Primary School held their first ‘Wear Red’ fundraiser in support of Children's Heart Surgery Fund. The idea to do it began when one of our Year 5 pupils told her friends all about her little brother, Theodore. He attends our nursery and...