Monday 16th - Tuesday 17th, September 2024
Monday 16th - Tuesday 17th, September 2024
THE SAVE OUR SONS DUCHENNE FOUNDATION
2024 NATIONAL DUCHENNE CONFERENCE
EARLY BIRD, SAVE UP TO 50% ENDS IN:
EARLY BIRD, SAVE UP TO
50% ENDS IN:
We are so excited to bring the 2024 National Duchenne Conference, scheduled for Monday, September 16th, and Tuesday, September 17th, at Waterview in Bicentennial Park, Sydney.
This conference will feature some of the most prominent national and international industry experts and healthcare professionals, who will impart their knowledge about Duchenne.
The conference aims to give parents, young men living with Duchenne muscular dystrophy, and professionals an interactive experience with Australian and international experts.
Our team is working hard on crafting a comprehensive program to provide a well-rounded understanding and update of the Duchenne landscape.
More details about the conference and how to secure your participation will be released in the upcoming weeks.
The conference is of significant importance for both families affected by Duchenne and industry professionals, and we, as the peak body for Duchenne in Australia, are proud to be hosting it. We hope to see you all there!
FAQ
Need Help? Please read below for detailed assistance.
The Venue
Registration
Pricing
Financial Assistance
Streaming/Recording
Miscellaneous
If we get a question that is not answered in our FAQs, we will add it to the list. Keep an eye out for updates on our website and social media.
INTERNATIONAL speakers
Pre-conference Materials
Video Resources
The following short video explainers will refresh our general understanding and terminology of genetics and the respiratory system. Our Presenters will not be explaining these basics.
You will maximize your participation during the conference if you have viewed and refreshed some terminology.
Remember these animations contain deficit medical language and median statistics, which are anticipated but not exactly predictable due to the wide heterogeneity in individual patients with Duchenne and Becker muscular dystrophy.
They feature almost none of the many skills and abilities that people with Duchenne will attain and retain.
DMD: The Pathogenic Gene of Duchenne Muscular Dystrophy
(3 Min)
Cough (3 Min)
C-PAP/BiPAP (3 Min)
TEXT RESOURCES
Glossary of Genetic & Genomic Terms
Did you know there are 4 conditions known as Dystrophinopathies :
- Duchenne muscular dystrophy (DMD)
- Becker muscular dystrophy (BMD)
- X-Linked Dilated Cardiomyopathy (XLDCM)
- Manifesting Carriers
Unofficially, we know that Carers (Family) are impacted emotionally socially, physically, economically and more.
Duchenne affects approximately 1: 5,000 live male births (LMB) and approx. 1: 50 million females. Becker affects 1: 18,000 male births. Duchenne is a rare genetic condition, and we learn many new medical and genomic terms as we grow in our understanding.
To help us all, particularly health consumers, the online NIH Talking Glossary will give you access to an easy-to-understand multimedia glossary of 250 terms in alphabetical order. Try it any time to aid your understanding.
Talking Glossary (Website Link)
Talking Glossary (PDF Version)
The Australian Clinical Trials Glossary (PDF Version)
Registration Costs
Early Bird Discounts vs. Standard Rates
Discounted Early Bird Prices Valid Until July 7th; Standard Pricing from July 8th


Conference Sponsorship Prospectus
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