Digital Mito Meet-up

Mito meet-ups are led by mito community members and offer you the opportunity to connect with the mito community. Get to know your hosts: Shelley grew up in South Africa, but in 2010, she moved to Tasmania. On the other hand, Matthew lives in Melbourne, Victoria. Both Shelley and Matthew have been active members of…

Digital Older Adult Mito Meet-up

Mito meet-ups are led by mito community members and offer you the opportunity to connect with the mito community. Get to know your host: Pam was diagnosed with mitochondrial disease (mito) in 2011 after showing signs and symptoms for many years. Despite Pam’s health, she remains an active volunteer with the mito foundation in the…

Digital Mito Meet-up

Mito meet-ups are led by mito community members and offer you the opportunity to connect with the mito community. Get to know your hosts: Shelley grew up in South Africa, but in 2010, she moved to Tasmania. On the other hand, Matthew lives in Melbourne, Victoria. Both Shelley and Matthew have been active members of…

Mito Connect Call: Supporting kids at school

Our first Mito Connect Call for 2024 will discuss supporting children living with mito at school. Whether your child is starting school, changing schools, or continuing their educational journey, it is important to connect with your child's school and teachers to discuss their individual health and educational needs. We will also look at new resources…

Digital Older Adult Mito Meet-up

Mito meet-ups are led by mito community members and offer you the opportunity to connect with the mito community. Get to know your host: Pam was diagnosed with mitochondrial disease (mito) in 2011 after showing signs and symptoms for many years. Despite Pam’s health, she remains an active volunteer with the mito foundation in the…

Digital Mito Meet-up

Mito meet-ups are led by mito community members and offer you the opportunity to connect with the mito community. Get to know your host:In 2016, Bec received a diagnosis of mitochondrial disease (mito) after experiencing ongoing symptoms for several years. Bec understands first hand the isolation that comes with living with mito. She lives on…

Digital Mito Meet-up

Mito meet-ups are led by mito community members and offer you the opportunity to connect with the mito community. Get to know your hosts: Shelley grew up in South Africa, but in 2010, she moved to Tasmania. On the other hand, Matthew lives in Melbourne, Victoria. Both Shelley and Matthew have been active members of…

NDIS Webinar Series: Meet a local area coordinator

Held Online via Zoom.

Our new National Disability Insurance Scheme (NDIS) webinar series kicks off with the opportunity to meet a senior local area coordinator. Local area coordinators support people in accessing and using the NDIS and ensure people with disabilities have the support they need to live their lives. This webinar will be facilitated by Mito Foundation's NDIS Navigator,…

Digital Mito and NF Parent and Carer Support Group

Mito Foundation and Children’s Tumour Foundation are delighted to partner for this dedicated parents and carers support group We welcome you to join a safe space to connect, share experiences and offer support to others raising a child with mitochondrial disease (mito) or neurofibromatosis (NF). Scroll to the bottom of the page to register for…

Digital Older Adult Mito Meet-up

Mito meet-ups are led by mito community members and offer you the opportunity to connect with the mito community. Get to know your host: Pam was diagnosed with mitochondrial disease (mito) in 2011 after showing signs and symptoms for many years. Despite Pam’s health, she remains an active volunteer with the mito foundation in the…