The awesome team at Enterprise Mobility all got behind their colleague Francesca this February to celebrate Wear Red Day.
Francesca’s son Luca was born with congenital heart defects and needed life-saving open heart surgery at just one week old.
Francesca said:
“We found out that something wasn’t quite right when we attended our 12 week scan.
“After an appointment with the fetal medicine and congenital cardiology teams at LGI, we were told that our baby had a ventricular septal defect and coarctation of the aorta and would need open heart surgery shortly after birth.
“When Luca was born, he was taken straight to the neonatal ward at Leeds Children’s Hospital where he was put on medication and monitored closely. He was there diagnosed with a Hypoplastic aortic arch, multiple VSDs and atrial septal defects. At one week old, Luca underwent open heart surgery.

“After eight agonising hours, we received a phone call to say that the surgery had gone well, they had managed to close Luca’s chest. This was amazing news as we were told to plan for it still being open and him needing a second surgery to close it after the swelling of his heart had gone down.
“We were also informed to prepare ourselves to see him for the first time, as he was still on a ventilator and connected to multiple machines. I just remember seeing him and being so grateful that he was still alive.
“Luca spent the following 10 days on PICU, where he had ups and downs.

“He was extubated 2 days post-surgery but was struggling to breath on his own, so he was put on a BiPap machine to help.
What is a BiPap mechine? If you have trouble breathing, a BiPap machine can help push air into your lungs.
“He then moved to the high dependency unit for two nights and finally onto the children’s cardiac ward (L51) where we were able to sleep by his side for the first time since he was born.
“Our little heart warrior also had to have a keyhole procedure in November 2024. He is such a happy boy and thriving, we cannot thank the staff at the Leeds Congenital Heart Unit and CHSF enough for saving our boy!”
Feeling inspired? Want to do your own fundraising for CHSF?
Request your fundraising pack today and find out more about supporting our charity! Our dedicated team are there for you every step of the way.
Amy’s Story
Amy’s daughter received open heart surgery at just 11 weeks old. Amy's little one is now three years old and Amy tells us all about her daughter’s CHD journey to date. Amy is also pregnant and knows her baby is already a heart warrior too. Amy, known online as...
Beau’s Story #BabyLossAwarenessWeek
written by mum Tilly-May “Back in February of this year (2024) we went for our 20-week anomaly scan at Bassetlaw. Unfortunately, a clear view of Beau’s heart could not be seen so we were sent to Leeds General Infirmary so the cardiology team there (who are one of the...
Game4Hearts: Jessica
Jessica was born with a hole in her heart and had open heart surgery when she was 8 years old. During her time in hospital, gaming provided a huge relief, joy and distraction from her treatment and continues to play a big part in her life.In 2021, Jessica decided to...