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We are very proud and excited to have had The CDH Patient Perspective Journey published in Frontiers in Pediatrics (neonatology section) in February 2023. We
CDH2022 is a follow on from previous symposia that is this time being held in Glasgow, Scotland. Bringing together Medical professionals, Patients Organisations and Researchers,
New guidelines to improve pregnancy trials will pave way for novel therapies for women and babies. A new grading system to monitor complications during clinical
Chairperson of CDH UK Beverley Power, along with other Rare Disease experts wrote to The Lancet to voice their concerns of a no deal Brexit
Many years ago a team based in Leuven, led by Professor Jan Deprest, set out on an incredible journey with the help of a little
CDH UK is very proud to be a founding member of ERNICA which is just one of many European Reference Networks (ERNs). ERNICA was established
WHAT IS THE GLOBAL PAEDSURG PROJECT? It is a multi-centre prospective cohort study of congenital anomalies to compare outcomes between LMICs and high-income countries (HICs) globally.
DHREAMS – what does the Acronym stand for? Diaphragmatic Hernia Research Exploration Advancing Molecular Science Where is the study based? The study is based at
CDH UK is proud to be a sponsor for the upcoming CDH International Meeting for Medical professionals and associated organisations on the 14th and 15th
We are very pleased to be able to announce that CDH UK has agreed to fund the following research projects that have undergone a peer
We are pleased to invite applications for Research Grants from the CDH UK Research Fund via our partner Sparks Children’s Medical Research Charity, as from
Wednesday 11th December 2014 saw MBRRACE UK launch it’s first confidential enquiry report into CDH to a large audience of clinicians, healthcare workers, public bodies,
June 28th is CDH Awareness Day Here is what we have going on! ‘WEAR 4 AWARENESS’ – encouraging everyone to wear a CDH Awareness item
On 15th My 2012 we launched a campaign requesting Government Funding for research into the cause of CDH. We require 100,000 signatures by this time
Here at CDH UK we know how important it is to find the cause (or causes), prevention and improved treatment and management of Congenital Diaphragmatic Hernia
We are currently helping researchers with finding participants for ‘The Bracelet Study’. Was your baby a non-survivor and taking part in any NICU clinical trials or
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