North West, North Wales & The Isle of Man Congenital Heart Disease Network, Alder Hey Children’s NHS Foundation Trust Email:
Join us for a new ❤️AEPC Heart beats for education - #Pregnancy in complex #CHD
🤰🏼Case presentation
🫀Pregnancy in Fontan
❓Challenging cases & key learnings
🗓️ Join us on 3 June 2026 | 17:00–18:30CEST
🔗 https://bit.ly/3OFXBse
#PediatricCardiology #YoungAEPC #ACHD
As a CHD patient, you may have been told to avoid certain activities or be concerned about side effects but carefully-chosen exercises suitable for your health conditions, will provide benefits that outweigh the risks.
Read more in our Exercise leaflet:
https://sfhearts.org.uk/leaflets/
Living with CHD means you need to be mindful in the heat. High temperatures can put extra strain on your heart so take care of yourself...
💧 Stay hydrated
🧢 Wear a hat and light clothing
⛱️ Stick to the shade or stay indoors
📱 Let someone know if you feel unwell
February 12, 2026
October 27, 2025
October 3, 2025
On this page you will find all of the relevant documents to support the Network Patient and Public Voice Group
This document explains the purpose and structure of the group. It helps everyone to understand the group’s role, how it works, and what is expected from its members.
This is a step-by-step overview of how to become a Patient and Public Voice Representative.
We recommend that you have a read of the role description first. If after doing this you would like to apply to join the PPV group then download this form and fill it in. You can send the completed form back to our Network Support Officer at: northwestchdnetwork@alderhey.nhs.uk
This is an advert that can be downloaded and printed locally to be displayed in hospital waiting rooms and wards etc. It can be displayed in any clinical area where patients and families might see it and be interested in joining.