The Children’s Heart Federation is dedicated to helping children with congenital or acquired heart disease and their families in Great Britain and Northern Ireland.
We are a parent-led charity consisting of more than twenty organisations, many of which are registered charities whose main aim is the support of families of children with heart conditions.
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Are you a young person who will soon transition to receiving support from an adult multidisciplinary team with congenital heart disease (CHD) specialism? Please share with CHF about what has worked well for you and what you would like to see improved — literally. Your here & now reality, experience & views of CHD are […]
An international research study noted in the Karolinska Institutet has focused on new fathers’ concerns including: money upbringing the health of their child. CHF would like to hear from our new fathers on their views too. Please share your experiences via firstname.lastname@example.org or via our Facebook page. We’d like to start a conversation on this […]
24/11/16 Congenital Heart Disease (CHD) & Disability Living Allowance (DLA) meeting at Parliament on 29 November 2016
Tuesday 29 November 2016 will bring together national children’s heart and adult congenital heart charities to a meeting in Parliament to obtain MPs’ support in getting children’s heart disease recognised in the Disability Living Allowance Assessor Pack. We need your help to get as many MPs to attend the meeting as possible. The event will […]
Children’s Heart Federation:
Whitechapel Technology Centre
75 Whitechapel Road
Freephone Infoline :
0808 808 5000
(9.30am – 4.30pm Mon to Fri)
Office Tel :
020 7422 0630 (9am-5pm Mon to Fri)