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This Christmas, help us to fight for a brighter future for the Thodes

Christmas is a time of togetherness. But families with mitochondrial disease (mito) don’t know how many Christmases they’ll share.

Last Christmas was stark for the Thode family.

They thought it would be their last together.

Mum Bec, and her children Lachlan and Ellie Thode all suffer from mito. It’s one of the most commonly diagnosed genetic diseases.

Mito is debilitating and life threatening. It robs the body’s cells of energy. It can cause multiple organ dysfunction and failure, fatigue, muscle pain and blindness.

This year, with your help, we can bring hope to families like the Thodes so that Christmas is a time of joy.

Your gift can light the path for Aussie families with mito


Can connect families with our helpline when they need it most.


Can fund a 1 hour consultation with our registered Pathways Telehealth Nurse


Supports our NDIS Navigator in helping people with mito access critical funding for their care. 

Donate and make a difference today 

You can help fund critical support services — a lifeline for people impacted by mito.

With early intervention and the right support, we can improve the lives of those with mitochondrial disease.

"From the first weeks of my diagnosis, the Mito Foundation team has been incredible. They've helped us understand this disease and get NDIS support. Mito is heartbreaking; it turns all our lives upside down. I wouldn’t be where I am today without the Mito Foundation."   Bec

About Mito Foundation

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