From being diagnosed with CHD at just 3 days old to overcoming multiple heart surgeries, Abraham is a true heart warrior!
As well as funding our life-saving Heart Unit where he was treated, Children’s Heart Surgery Fund have played a crucial role in supporting Abraham and his family on his journey so far.
Abraham’s mum, Katherine, said:
Abraham was diagnosed with CHD when he was three days old. They found he had multiple heart defects, and we were rushed across to Leeds from Jessops Wing in Sheffield the following day.
Due to Abraham being born prematurely, he was too small for surgery, so we were cared for on neonates for three weeks until he had his first open heart surgery in “the hybrid” theatre.
For the first 12 weeks of his life, we thought he was going down the single ventricle route of surgery but by some miracle on the morning of his second open heart surgery his surgeon, Mr Jaber, came and told us he thought he can do a full heart repair.
A long 10 hours later, Abraham was out of surgery. Mr Jaber had worked his magic and he had repaired our boy’s heart.
However, his recovery wasn’t smooth to start with and one week later he had a pacemaker fitted as he was still in ‘heart block’ following his repair.
Heart block is a condition where the heart beats more slowly or with an abnormal rhythm. It’s caused by a problem with the electrical pulses that control how your heart beats.
A pacemaker is a small electrical device that’s implanted in the chest or abdomen. It’s used to treat some abnormal heart rhythms (arrhythmias) and sends electrical pulses to the heart to keep it beating regularly.
After this, Abraham flourished, and he grew stronger and stronger.
As we left hospital the aim was to get Abraham to his first birthday before we discussed any further surgery. Abraham way exceeded this and on the 5th January 2024 he had his third open heart surgery, aged 4 years 7 months old.
In this surgery he had a resection of his aortic valve membrane and his pacemaker replaced (he is pacing himself and was pre-surgery too).
On writing this, he is now 20 days post-surgery and doing amazingly!
Children’s Heart Surgery Fund have helped us so much throughout our journey as a family, navigating the new world of CHD.
Without their support we wouldn’t have been able to stay close to Abraham during his time in hospital. His first admission was for 16 weeks. We were helped financially during our first admission too, which was a great help as living in hospital isn’t cheap.
Abraham also loves his Katie Bears and certificates!
CHSF gives us opportunities to meet other heart mums and dads. We enjoy meeting and talking to other parents who share the same experiences as us. As Abraham gets older, I believe he will benefit from meeting other children who have gone through what he has too.
On our latest admission it was lovely to meet Family & Youth Support Worker, Lucy!
Wear red for REGGIE
"Without Children’s Heart Surgery Fund, Reggie wouldn't be here." Michelle, Reggie's mumWritten 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...
In memory of Sian Firth
written by Sian's sister, Rachael My son Samuel was born on 30th October 2014 in our local hospital. It was clear straight away there were complications, but no one was sure what they were. Following various tests, he was transported later that day to the...
Revolutionary valve procedure performed in Leeds
In June this year, the Congenital Cardiology Intervention Team performed a pioneering procedure by implanting a Venus P pulmonary heart valve into an adult congenital heart disease patient. This was the first implantation of this revolutionary valve in Europe after it...