Duchenne Foundation

Duchenne Foundation’s Melbourne Symposium 2014

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 […]

Read full story Comments are closed
Annual Scientific Report 2012

Annual Scientific Report 2012

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: https://www.ann.org.au/annual-scientific-report-2012/.  

Read full story Comments are closed
432638114_640

World’s first petition signing bionic arm

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 […]

Read full story Comments are closed
12th Asian & Oceanian Myology Center (AOMC) Scientific Meeting (6th to 8th June, 2013)

12th Asian & Oceanian Myology Center (AOMC) Scientific Meeting (6th to 8th June, 2013)

The 12th Annual Asian and Oceanic Myology Centre (AOMC) Scientific Meeting – 6th – 8th June 2013 Abstract Submission deadline:March 31, 2013 Early bird registration deadline:May 24, 2013 Visit the AOMC conference website to register and for further information.

Read full story Comments are closed