Contact Info

North West, North Wales & The Isle of Man Congenital Heart Disease Network, Alder Hey Children’s NHS Foundation Trust Email:

northwestchdnetwork@alderhey.nhs.uk

Our X Feed

📢 Are you interested in joining the NW CHD Network Patient &Public Voice Group or just want to know more about the excellent work they do? Join our informal information session via Teams on 09/09/26 #chd #ACHD #paediatriccardiology ❤️❤️❤️

https://www.northwestchdnetwork.nhs.uk/all-about-our-patient-and-public-voice-group-ppv/

If you become our supporter on easyfundraising, you'll raise free funds for Somerville Heart Foundation simply by shopping online.

It's easy to set up - visit the website or download the app and choose Somerville Heart Foundation.

https://bit.ly/4ztaGwc 💙

Empowering hearts globally (EHG) launches their first 'Fundamentals in pediatric & congenital cardiology' boot camp!
A comprehensive 4-week online course designed to build practical knowledge & clinical confidence in pediatric cardiology. 
Find out more: https://empoweringheartsglobally.org/2026-fundamentals-course/

Our private online communities offer support for people affected by CHD:

❤️ Somerville ACHD Patient Group 1 – for CHD patients
❤️ Heart Families – for family, friends and carers

Join or become a member for free: https://sfhearts.org.uk/sign-up/

News

Heather

Hello, my name is Heather, and I was born with Tetralogy of Fallot. I had my original heart op in 1979 at the old Mrytle Street Children’s Hospital in Liverpool and as an adult I have had a pulmonary valve replacement and an ICD fitted.

I’ve lived in different parts of the North West including Lancashire and Merseyside, and am currently based in South Cumbria. I work in tourism marketing but have also done a variety of different journalism and communications roles, hopefully skills which I can bring to the PPV group.

I put myself forward as a volunteer for the PPV group in early 2024 because I have benefited directly from congenital heart services throughout my life, and I wanted to do something positive for fellow patients and their families.

The group came to my attention after I attended a patient information day in 2023. I think it’s a really important way to put patients’ needs and opinions at the forefront of care for people – of all ages – with congenital heart problems.

Skip to content