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Supporting those with an inherited metabolic disorder and their families so that they can thrive and live their best life.

We raise awareness of inherited metabolic disorders like PKU and other rare IEpMs, we build programs and develop resources from newly diagnosed infants through all life stages.

“MDDA provides me with a window to what is happening in Australia with regards to my PKU and allows me to reach out to others”

Philip

“As a MDDA member I feel connected and not alone with my son’s diagnosis. It eases my mind and reduces my anxiety. I know I will get help if I need it”

Melissa
Diagnosis

Diagnosis

A metabolic disorder is diagnosed by the heel prick test. 

Find out more here

Diet

The Low Protein Diet is for life for people living with an inherited metabolic disorder.

Find out more here.

Care and support

Care & Support

The MDDA offers various resources and programs to assist in diagnosis and management.

Get Involved

Get Involved

Help increase the awareness of inherited metabolic disorders. Find out more on how you can become a member, volunteer or donate

News Room

Events

  • 2025 NSW National Family Retreat

    2025 NSW National Family Retreat

    Location: Fairmont Resort, Blue MountainsDate: November 21-23, 2025 Join us for an unforgettable weekend at the 2025 MDDA National Family Retreat, held at the stunning Fairmont Resort in the Blue […]

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  • Christmas Appeal 2024

    Christmas Appeal 2024

    This Christmas, we invite you to be part of something truly special.  Metabolic Dietary Disorders Association Inc (MDDA) are the national peak consumer body dedicated to supporting, educating, connecting, and representing […]

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  • Upcoming 2024 MDDA Annual General Meeting 

    Upcoming 2024 MDDA Annual General Meeting 

    📢 Upcoming 2024 MDDA Annual General Meeting 📢 We’re excited to announce that the MDDA Annual General Meeting (AGM) will be happening soon! This is an important opportunity for our community to […]

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  • MDDA Adult PKU/IEM Lived Experience Support Group

    MDDA Adult PKU/IEM Lived Experience Support Group

    Join us online monthly for our MDDA Adult PKU/IEM Lived Experience Support Group where we’ll chat about all things PKU, IEM, and beyond! 🗓 When: First Wednesday of every month. 🕒 Time: 7:30 PM – 8:30 […]

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🌟 A Huge Thank You to Our Amazing Sponsors and ...

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Are you up for the Challenge in 2024!? ...

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🌍 Celebrating Rare Disease Day 🌍

Rare
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MDDA raise awareness of inherited metabolic ...

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MDDA RETREAT REGISTRATIONS ARE NOW OPEN!
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Happy Mother’s Day to all the wonderful IEM Mums! ...

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Happy Easter from all of us at MDDA!

We
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BREAKING NEWS - An important win for the ...

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Returning for 2023….The Great Protein Challenge ...

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SAVE THE DATE - 2023 National Family Retreat
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2023 Reminder - Important Information About the ...

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Today is Rare Disease Day!

Rare Disease Day
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With the Summer holiday fun coming to a close, for ...

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IMPORTANT INFORMATION ABOUT THE IEM FOOD GRANT ...

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We wish you a Merry Christmas and Happy New Year ...

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THE RETREAT IS HERE!

Team MDDA touched
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The Power of Advocacy a win for equitable ...

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Team MDDA’s LowProHighTea!
 
Team MDDA
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MDDA is registered with the Australian Taxation Office as an Public Benevolent Institution. We are endorsed as a Deductible Gift Recipient (DGR). All donations over $2 are tax deductible.

Disclaimer: Information presented within this website is intended for general purposes only and should not be construed as advising on diagnosis or treatment of any medical condition, if you have interest in any of the foods or treatments contained within this website check first with a qualified health professional.

In the spirit of reconciliation the Metabolic Dietary Disorders Association acknowledges the Traditional Custodians of country throughout Australia and their connections to land, sea and community. We pay our respect to their Elders part and present and extend that respect to all Aboriginal and Torres Strait Islander peoples today.