Little Hearts Matter’s Youth Activity Weekend Is Back with a Bang!
For the first time in three years, the Little Hearts Matter Youth Zone has returned to its popular PGL activity weekend – bringing together young people with half a working
NATIONAL CONGENITAL HEART DISEASE AUDIT (NCHDA)
NATIONAL CONGENITAL HEART DISEASE AUDIT (NCHDA)2022 Summary Report (2020/21 data) Published by National Institute of Cardiovascular Outcomes Research (NICOR) Excerpt: “This report summarises selected key findings from the National Congenital
‘The Fontan gave me time and hope’ – Kirsty’s Story
Kirsty shares her story of life as an adult Fontan patient
I’m on a mission to do as much as I can – Hannah’s Story
LHM Trustee Hannah Palmer shares a special update on her life as an adult with congenital heart disease in 2022.‘Today, Somehow, I’m a business owner’ – Jack’s Story
Jack, 28 with Hypoplastic Left Heart Syndrome shares his story.
An improved congenital heart assessment tool: a quality improvement outcome
Published online by Cambridge University Press: 02 May 2022 Kerry L. Gaskin, Liz Smith and Jo Wray Background: CHD was the most prevalent congenital anomaly (60.9 per 10,000, 95% CI 59.0–62.8) in
Taking your Baby home from hospital – Research Project
Taking your baby home after their first surgery is often a scary time. Understanding what to look for and what to seek help with can be confusing. The LHM teamHelena’s HLHS Story
Hey my name is Helena Grace, I am 17 years old and I was born with a very complex and rare heart condition called Hypoplastic Left Heart Syndrome, HLHS. For
LHM Awareness Week
“Thriving, not just Surviving.” From May 1st – 7th, the Little Hearts Matter family will celebrate our fourth annual Awareness Week. This year, we have created a social media campaign