who_we_are

Who we are

Syndromes Without A Name (SWAN) Australia provides information and support to families who have a child with an undiagnosed or rare genetic condition.

Discover more about SWAN Australia and how we were established. Let us introduce to our committee and discover our mission and vision for our future.

our_work

Our work

Learn more about what we do and our purpose and goals. Have our read of our strategic plan and read our submissions to get an understanding of how we advocate for change. And don’t forget to subscribe to our quarterly newsletters.

difference

Making a difference

Understand about the issues that SWAN families face and discover how we advocate for change.  You can partake in a research projects or simply just donate to make a difference so we can assist more families on their undiagnosed journey.

Genetic Testing

Genetic Testing

We are hoping to adopt Genome Sequencing into clinical medicine in Australia within the next 12 months. Read More.

Support

Support

Please T: 0404 280 441 or email info@swanaus.com.au if you would like more information about SWAN Autralia

Information

Information

For more information, please contact SWAN Australia of consult our useful website links or our SWAN brochure

Advocacy

Advocacy

We advocate for systemic change to make genome sequencing available on a clinical basis. Click here to learn more about our advocacy work.

Become A Member

Become a Member

Join SWAN today and support undiagonosed children and their families. Membership is free for SWAN families.

About Us

About Us

SWAN Australia provides information and support to parents/carers who have a child with an undiagnosed or rare genetic condition

Life is difficult enough when you have a child with a disability or medical condition, but when nobody can give you answers it is that much harder.

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