CHSF’s private community group on Facebook is a peer-support forum for heart families and patients to network with others who have had shared experiences.

The group consists of patients with congenital heart disease, parents and family members who find it an enormously supportive service. Many networks and friendships have been formed as a result of this private group. We are very proud to witness how our heart families help each other.

Me and my family were incredibly grateful for the support from CHSF’s Facebook community. We didn’t know what to expect during open heart surgery, and to receive both words and pictures of comfort was really reassuring.” — Mia, Heart Mum

Set up in 2010, the group currently has over 5,300 members. Members have to answer a few basic questions to join, to ensure it is the right group for them. Just like any other forum, the CHSF team monitor posts to make sure essential etiquette is followed.

The main benefits for members are that it can provide reassurance, companionship and basic information which doesn’t need medical input. The group is not a medical resource and does not provide medical advice. If we see a question which is medical, we refer members to the relevant hospital teams.

Speaking to other patients or parents of children with heart conditions can be a lifeline.

Get to know our new Family Support Worker, Sarah!

Get to know our new Family Support Worker, Sarah!

Because of your fantastic fundraising, this year we have been able to appoint a dedicated support worker for our heart families. Everyone, meet Sarah Cherry! Sarah will help our heart families to access services, provide practical support to families whilst being...

New MRI coil will save countless lives

New MRI coil will save countless lives

As reported in the Yorkshire Evening Post, babies being treated for congenital heart disease at Leeds Children's Hospital will soon have access to a new life-saving piece of kit - the first of its kind in Europe. The Morrisons Foundation has donated £25,000 to the...