Tour de ChIPS: How young people with chronic illness see it and how, through the RCH Chronic Illness Peer Support (ChIPS) Program, they shared this on a global scale in Paris

ChIPS the RCH Chronic Illness Peer Support program, is twenty one years old this year. Managed by the Centre for Adolescent Health, ChIPS brings young people together to share their experiences of chronic illness, create peer support networks and engage in activities that they may not get a chance to do otherwise. The program uses both Youth Participation and Peer Support models.

Options for the failing Fontan

The Australia and New Zealand Fontan Registry is the largest database of patients born with a single heart pumping chamber. The Fontan Registry has already allowed us to demonstrate that survival is far better than expected.

Three decades of hypospadias repair and still learning

Hypospadias is a common malformation in boys with potential long-term consequences. Despite better understanding of the malformation and refinement of surgery, the results can remain unsatisfactory, especially in proximal hypospadias. Prof Martin Koyle will present the journey of an experienced pediatric urologist involved in surgical correction and follow-up of patients with hypospadias.

Diversity in the Health Context – Bridging the Divide to Culturally Appropriate Care

Australian patients with low English proficiency are considerably disadvantaged compared to patients who are fluent in English; they stay in hospital longer, have higher readmission rates, and undergo more diagnostic tests. When these patients also have a disability or a mental health condition, the divide is even greater. ‘Diversity’ in the health context mainly translates to ‘disadvantage’ and inequality; this Grand Round will argue that we need to change the perception of ‘diversity’ as a problem, and embrace it as a solution.

Celebrating Women in Science

To secure Australia’s health and economy into the future, the talents of women in science are vital. In biology, over half of all Bachelor of Science and PhD graduates are women, yet there is only one in ten women at the senior levels of our universities and research institutes

Exciting Developments in the World of Cystic Fibrosis

Research at the Melbourne Children’s Campus was recently described in the New England Journal of Medicine as ‘leading to a paradigm shift in our understanding of lung disease in cystic fibrosis’.