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.
Mito Patients and Carers
Access services and information for diagnosed and undiagnosed mito patients and carers.
Learn MoreGet Involved in Fundraising
Help raise vital funds to support the mito community and help find a cure.
Learn MoreClinicians and Researchers
Medical information about mitochondrial disease, as well as research initiatives.
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Fundraiser Appreciation: Eview Group
Back in May, the Eview Group set out to tackle an exceptional feat; to walk 50kms (that’s 15kms more than The Bloody Long Walk) to raise awareness and funding for…
New National Mitochondrial Diagnostic Network
A team of mitochondrial researchers led by Professor David Thorburn has secured $3M in funding to establish a national network to improve mito diagnosis. The funding is part of the…
Patient Pathways Program – Sian’s Story
Last November, Sian Cave reached out to the Mito Foundation Patient Pathways Program after receiving a confirmed diagnosis of MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes). Michele, the foundation’s…
UPCOMING EVENTS
Digital South Australia Meet-up – September 2021
The Digital Mito Meet-ups are led by mito community members and offer…
Digital National Mito Meet-up – October 2021
The Mito Meet-ups are led by mito community members and offer you…
Digital New South Wales and Queensland Mito Meet-up – October 2021
Please note, if you are joining from New South Wales, the start…