by CHSF | Feb 14, 2025 | EVENTS, RUNNING
by CHSF | Feb 11, 2025 | FAMILY, LATEST NEWS, WHAT YOU'VE FUNDED
At CHSF, we know that a hospital stay can be overwhelming, and the impact of congenital heart disease (CHD) extends beyond medical treatment. That’s why our Family Support team is there to provide practical assistance, wellbeing support and moments of respite to...
by CHSF | Feb 7, 2025 | LATEST NEWS, REAL STORIES, WEAR RED DAY
17-year old Alfie’s family found out he had congenital heart disease (CHD) when he was just 2 months old. Following multiple procedures, Alfie is now enjoying life both as a teenager and keen LUFC supporter, as mum Kirsty tells us: “Alfie was only 7 weeks old when we...
by CHSF | Feb 7, 2025 | LATEST NEWS, REAL STORIES, WEAR RED DAY
We know it’s vitally important to share your journeys with congenital heart disease. Your experiences are both reassuring and educational for other heart families, and provide vital awareness for others. 3-year old Zak’s condition was found by complete coincidence,...
by CHSF | Feb 7, 2025 | LATEST NEWS, REAL STORIES, WEAR RED DAY
Alessia Mae is fast approaching her first birthday, but at birth she was sent urgently to her local hospital as she was critically low on oxygen and had open heart surgery at just a day old in Leeds. Mum Tierney tells the full story… “Alessia Mae was born on the 21st...
