Join us at the Surfair Conference & Events Centre Marcoola on Thursday 25th and Friday 26th May for the ANN Congress 2023. Registration and abstract information to follow very soon…
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The Duchenne Foundation Australia invites you to register your attendance for the Melbourne Symposium 2014, “A Breath of Fresh Air”. The conference provides an opportunity for patients, carers and health care professionals to come together with international respiratory and cardiac experts to give those affected by Duchenne, first-world knowledge and support. Program details are available […]
The inaugural Annual Scientific Report for the Centre for Research Excellence in Neuromuscular Disorders (CRE-NMD) and Australasian Neuromuscular Network (ANN) has been released! The report details our goals, activities, teamwork and achievements for the year of 2012. Please follow the link to find out more: http://www.ann.org.au/annual-scientific-report-2012/.
Save Our Sons and the Duchenne Foundation have launched the world’s first petition signing bionic arm in an effort to raise awareness for young sufferers of Duchenne Muscular Dystrophy (DMD). The robot arm was invented to do what many young DMD sufferers can’t – write. The arm takes its commands from the website,TheMostPowerfulArm.com, where visitors […]
Our goal is to ensure excellence in diagnostic methods and clinical management, and equal access to clinical trials and new therapies, for all individuals in Australia and New Zealand affected by neuromuscular disorders.
We can achieve our vision by establishing a cohesive, integrated neuromuscular network which enables people to work together across Australia and New Zealand, for the well-being of patients.