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  • About Mito
      • Mito Information – What is mitochondrial disease? Learn more about this rare disease.
      • Maybe it’s Mito – Information for individuals with suspected mitochondrial disease.
      • Mitochondrial Donation – An IVF technique with the potential to prevent mitochondrial disease in the next generation.
      • Personal Stories – Read inspirational stories of other people’s experiences with mito.
      • For Health Professionals – Information about mitochondrial disease for health professionals.
      • COVID-19 Information Portal – Information about COVID-19 vaccines, latest health advice and support resources.
      • Find A Health Professional – Locate a health professional with experience in seeing people impacted by mito.
      • Resource Hub – Helpful fact sheets, videos, expert presentations and third party resources.
      • Mito Community Voice – Understand the mito community’s role in shaping our work.
  • Managing Mito
      • For Newly Diagnosed – Information and services to help start your journey with mito.
      • For Health Professionals – Information to help understand, treat and refer people impacted by mito.
      • For Adults – Services and resources to empower you in your day-to-day life with mito.
      • For Parents and Children – Services and resources to help manage your family’s day-to-day life with mito.
      • Find A Health Professional – Locate a health professional with experience in seeing people impacted by mito.
      • Resource Hub – Helpful fact sheets, videos, expert presentations and third party resources.
  • Find Support
      • Helpline – Contact the Helpline to talk to a Support Officer for general advice or assistance.
      • NDIS Support – Access the NDIS Navigation Service for resources, education and 1:1 guidance on the NDIS.
      • Pathways Teleheath Nurse Program – Our Pathways Teleheath Nurse will work with you to develop a tailor-made care plan.
      • Mito Registry – Join the Mito Registry for access to new treatments, clinical trials and studies.
      • Mito Information Days – An in-person event offering presentations from mito experts and connections with others impacted by mito.
      • Mito Connect Calls – A digital monthly call featuring guest speakers and topics of interest to people impacted by mito.
      • Mito Meet-ups – A regular state-based call for people impacted by mito to connect, provide support and combat isolation.
      • Peer Support – Unique one-on-one support for individualised connections within the mito community
      • Government Support – Learn about subsidies, concessions and disability services available to people impacted by mito.
      • Grief & Loss Support – Grief can be a response to many situations when living with a chronic illness, visit this page for support resources and organisations.
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    • Mito Registry – Join the Mito Registry for access to new treatments, clinical trials and studies.
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  • About
      • Purpose and Vision – Learn about the foundation’s mission to enrich the lives of people impacted by mito.
      • Driving Change – Learn about the foundation’s advocacy and policy work.
      • Our Impact – Learn about research projects the foundation has funded.
      • Your Donations at Work – Learn how your donations have helped people impacted by mito.
      • Our People – Learn more about the individuals involved with the foundation, from mito community representatives to public ambassadors.
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      • Contact – Find out the various ways to get in touch with the foundation.
      • Affiliations – Learn about organisations that work with the foundation.
      • Annual Review – Access the annual review for a snapshot of the work done to provide support and hope to the mito community.
      • Opportunities – Find out about the latest opportunities to work or volunteer with the foundation.

Archive for January 2020

Leigh Syndrome International Consortium: Grant recipients announcement

By Communications User | 31/01/2020

The Leigh Syndrome International Consortium, a patient-driven research network steered by five of the world’s leading mitochondrial disease patient advocacy groups, is delighted to announce it will grant a total…

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Your Donations At Work – December 2019

By Communications User | 24/01/2020

Over the last six months your donations have made a substantial difference to people affected by mitochondrial disease (mito). You have enabled services to support patients today, while providing hope…

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Recent Posts

  • Genetic testing for mito announced in Federal Budget
  • Government committee recommends genomic testing for mitochondrial disease be funded by Medicare
  • Introducing the Newly Diagnosed Support Project
  • Showcasing the Peer Support Network
  • How the mito community shaped Mito Information Days

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    Mito Foundation supports people affected by mitochondrial disease (mito), funds essential research into the prevention, diagnosis, treatment and cures of mitochondrial disorders, and increases awareness and education about this devastating disease.

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