This is Karim’s story, shared by mum Kamila. Karim was born in Scunthorpe and was blue-lighted to Hull and then Leeds after a congenital heart defect was discovered.
Children’s Heart Surgery Fund supports the Leeds Congenital Heart Unit, helping provide the care and equipment needed throughout his treatment.
“Throughout my pregnancy I was closely monitored because of my type 1 diabetes, having weekly scans from 26 weeks until I gave birth. Every time I was reassured that my baby boy was healthy.
“On the 4th April at 10:14am, our beautiful boy Karim was born. He cried for just five seconds… and then suddenly everything went silent.
“I remember lying there asking my husband, ‘Is he okay? Why haven’t they shown him to me?’ Within minutes the room filled with doctors. I was told he needed 100% oxygen and had to be taken straight to NICU.
“Because I had a C-section, I didn’t get to see my baby until eight hours after he was born, when the Embrace team briefly brought him to me before transferring him to Hull. I only had 20 minutes with him and, with all the wires covering his tiny body, the only thing I could gently touch was his little nose. Then he was taken away. That night my newborn baby and I were in two different cities – the hardest night of my life.
“24 hours after giving birth, I finally got to kiss my son for the first time, but he still couldn’t breathe on his own. Soon after, we were told he needed to be transferred again to Leeds after doctors found an abnormality with his heart.
“At Leeds Children’s Hospital we were told Karim had a rare heart condition called TAPVD and ASD. At just three days old, he needed open heart surgery the next morning – his only chance of survival. Hearing those words broke my heart, but I put my full trust in Allah SWT. When I met Karim’s surgeon, Dr Pelella, I felt a sense of calm and hope.
“Karim’s recovery was a rollercoaster, but he proved to be a true warrior. His surgery was successful thanks to the incredible surgeon and the amazing teams at PICU L47 and Ward L51. I will forever be grateful to every doctor and nurse who helped save my baby’s life.
“During this time we stayed at Eckersley House so we could stay close to Karim during the hardest time of our lives. Being surrounded by other families going through similar journeys reminded me that we weren’t alone.
“Today I look at my baby boy with nothing but pride. He is my little fighter, and I will forever be proud of him.
“The amount of support I got from Children’s Heart Surgery Fund during this extremely difficult period felt like a sense of calmness in the midst of all the chaos. I’m eternally grateful for all the support I have received from them and couldn’t have done survived the way I did without them!”
Your donations provide the ‘calmness in the chaos’ for heart families from all across our region facing CHD.
Please help us continue to support more families who need us.
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 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
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...


