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!”

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Daisy

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

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...

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...