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

An exciting opportunity has arisen to for an experienced cardiac nurse to come and join the #ACHD nursing team in the #Northwest @LHCHACHD @LHCHFT @NwchdN

Details below👇
https://www.nhsjobs.com/job/UK/Merseyside/Liverpool/Liverpool_Heart_Chest_Hospital_NHS_Foundation_Trust/Adult_Congenital_Heart_Disease_ACHD/Adult_Congenital_Heart_Disease_ACHD-v8219528?_ts=565

Personal Health Passports are a valuable resource for anyone with CHD🥰

There's room to record:
The name of your heart condition
Hospital details
Medication & much more

For a small donation to cover P&P we can send these to ACHD patients - email info@sfhearts.org.uk

This week we're looking at interruption of the aortic arch♥️

Surgery is necessary to repair the aorta and close the VSD.

We are here to support young people and adults born with a heart condition🩵♥️

Heart image credit: Leeds Teaching Hospitals NHS Trust.

📢 New date announcement for the Patient & Public Voice Group information session.
❤️Come along and find out how your voice can be heard and make a difference to paediatric cardiology and ACHD services.
Please click on the link to register:
https://forms.cloud.microsoft/e/yqCBwX6Hft

❤️❤️

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.

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