Information and Support

The Australian NPC Disease Foundation offers resources, information, and connections for individuals with NPD, their families and caregivers, as well as healthcare professionals and service providers who assist them in living a healthy life

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About Us

Discover the story behind the foundation's establishment and the incredible individuals who selflessly dedicate their time to assist those with NPD.

Contact Us

Discover how to get in touch with the Australian NPC Disease Foundation.

Conference

Learn more about our Annual Conference for Niemann-Pick disease held online and in-person in Melbourne.

Our Advocacy Partners

Partnering with these organisations helps ANPDF expand its reach, resources, and impact in supporting the Niemann-Pick disease community.

Video Series

Meet the incredible Aussie warriors who are fearlessly fighting against NPD and stay up-to-date with our latest conference sessions. Let's go!

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ANPDF Blog

Check out the latest in community, research, and fundraising updates.

NP-C Corner

Follow Ellie as she explores the many aspects of Niemann-Pick Disease.

Useful Links

Find valuable resources, support organisations, and informative articles.

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Four mums to children diagnosed with Niemann-Pick disease type C

Four mums to children diagnosed with NP-C at the Minds in Motion 2024

Together we can make a difference

Join Us

Become a member of the Australian NPC Disease Foundation (ANPDF) and join a dedicated community committed to raising awareness and supporting those affected by Niemann-Pick disease. As a member, you’ll receive exclusive updates, resources, and opportunities to participate in our events and initiatives. Your membership helps us drive research, advocacy, and support for the NPD community.

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