News

Wear red for REGGIE

January 17, 2023 Latest News

“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 […]

“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.

SIGN UP TO WEAR RED DAY

Share

Latest News

All the latest news, stories and support from Children’s Heart Surgery Fund
Real Stories
A selfie of Haydn and his mum Nicola, smiling. Haydn is in a wheelchair and they are sat in the hospital rooftop garden
November 3, 2026
Haydn
Diagnosed with severe aortic stenosis as a teenager, Haydn faced important decisions about his care before undergoing open heart surgery.
Adult | ACHD
Steven with his wife and two children in front of a scenic background. There is a mountain and sea behind them.
October 30, 2026
Steven
Steven was born in 1990 and had heart surgery in Leeds when he was a baby. Now 36 he wants to share his experiences to give hope to others.
Real Stories
Albert
October 23, 2026
Albert
Mum, Ellie, tells us about how their CHD journey began at the 20-week scan, where son Albert was diagnosed with Tetralogy of Fallot (ToF).
CHSF
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.