Carer benefits and legal services Cdh Uk (Congenital Diaphragmatic Hernia)
Contact us
About
CDH UK consists of families, friends and medical professionals affected by Congenital Diaphragmatic Hernia (CDH)
CDH UK was founded and registered with the Charity Commission in 2003 by Brenda Lane. It was initially formed as a small support group to provide parents and families faced with a CDH diagnosis with a friendly and informal support network of other parents and families who had endured similar experiences, and who could offer emotional support and share experiences with them.
Today CDH UK has grown into an established registered charity that still offers the same friendly, informal support, but that now also has many more resources and offers information and advice on CDH from diagnosis to childhood and beyond, through different types of media such as the internet and written publications.
Opening times
Monday to Sunday 8am - 10pm
Catchment area
Nationwide
Target group
families, friends and medical professionals affected by Congenital Diaphragmatic Hernia (CDH)
Further information
Whether your baby is newly diagnosed, just born, in NICU, at home or sadly no longer with you, we are here to support you and to try to help you in any way that we can. At any point you may have questions or require help and advice on a range of subjects and issues, so don’t feel alone or confused, contact CDH UK. We also run a Home to Hospital scheme which provides financial help towards costs for traveling to and from hospital appointments and visits and for parking associated with these.
Referral method
Self referral
This information was supplied by Serco Global Services on 1 April 2025.