Dr Hunt (FRACP, MRCP (UK), MMed, PhD) is the Director of the Department of Neonatal Medicine at The Royal Children’s Hospital in Melbourne
What is Congenital Diaphragmatic Hernia?
Dr Nadia Badawi, Consultant Neonatologist.
The diaphragm is a muscle that helps us to breathe and separates the chest cavity from the abdominal cavity. It develops in early foetal life. Congenital diaphragmatic hernia is the absence of the diaphragm or, more commonly, the presence of a defect in the diaphragm.
It can occur on either the left or the right side, or be bilateral, but is most common on the left (80%).
As there is a defect in the diaphragm, the abdominal contents including the stomach, intestine, liver and spleen can be displaced into the chest cavity. CDH is usually an isolated condition, although other congenital anomalies, most commonly cardiac, may be associated and influence the prognosis.
Since these organs are in the chest cavity and not where they are supposed to be, the lungs have insufficient space to grow normally and are therefore smaller than they should be. The determinants of survival include the degree of underdevelopment/undergrowth of the lung and the supplying blood vessels with associated pulmonary hypertension, as well as the gestation of the
Want to Talk?
If you need to speak with one of our volunteers, complete this form and we’ll contact you as soon as possible. You can also call us on 1800 149 562.
CDH Australia is run solely by volunteers and relies heavily on donations.
All donations over $2.00 are tax deductible and funds help us to:
- provide telephone and online support for families affected by CDH
- facilitate an annual forum for families and medical professionals to share knowledge and provide support
- provide training to our volunteers and produce support booklets
- support and help fund research and clinical programmes in relation to CDH
All donations can be made in honour or memory of individual CDH children.
CDH thanks you for your kind donation and continued support.
CDH Affects 1 in every 5,000 Live Births in Australia.
We’re a national organisation, providing support for families, friends & medical professionals affected by Congenital Diaphragmatic Hernia (CDH).
We support families expecting a baby diagnosed with CDH, families caring for a CDH child, adults with CDH and bereaved families, seeking to minimise the social, financial and mental health impacts.
Our support includes;
- telephone and email support
- information booklets
- online forums
- parent-to-parent matching
- annual forum held in October
If you’re experiencing, or have experienced CDH, please become a part of our community to access valuable peer support and information. You access support through this website, call us or join our Facebook groups.
Latest News from CDH Australia
Babies born with CDH have a 40-50% mortality rate
CDH Families Thank Medical Professionals
Would you like to thank someone, too? Tell us your story today!