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

Card image cap

Access services and information for diagnosed and undiagnosed mito patients and carers.

Learn More

Get Involved in Fundraising

Card image cap

Help raise vital funds to support the mito community and help find a cure.

Learn More

Clinicians and Researchers

Card image cap

Medical information about mitochondrial disease, as well as research initiatives.

Learn More
News

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…

Read More...
News

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…

Read More...
News

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…

Read More...

UPCOMING EVENTS

Digital South Australia Meet-up – September 2021

The Digital Mito Meet-ups are led by mito community members and offer…

Event Details

Digital National Mito Meet-up – October 2021

The Mito Meet-ups are led by mito community members and offer you…

Event Details

Digital New South Wales and Queensland Mito Meet-up – October 2021

Please note, if you are joining from New South Wales, the start…

Event Details