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Mito Foundation and Children’s Tumour Foundation are delighted to partner for this dedicated parents and carers support group

Mito Foundation logo and Children's Tumour Foundation logo

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).

Why are Mito Foundation and Children’s Tumour Foundation working together?

The mito and NF communities share many similarities. By creating a space for these communities to meet, we hope they can share their experiences, strength and hope for the future. Come along to make new connections in our combined community.

Meet your hosts

Photo of Preeti Raghwani

Preeti Raghwani

Mito community member

Photo of Diane Cass

Diane Cass

Mito community member

Photo of Ruth Lindsay

Ruth Lindsay

from Children’s Tumour Foundation

Event information

Date

Sun 25 Aug 2024

Start Time

11:00 am AEST

End Time

12:00 pm AEST

Below are the start times based on State/Territory:
• QLD, ACT, NSW, TAS, VIC: 11.00 am
• SA, NT: 10.30 am
• WA: 9.00 am

Joining an online event

Our online events are held via Zoom. Please read our Mito Connect event guidelines for more information on accessing Zoom. If you require assistance to attend our events please get in touch. Contact us at supportservices@mito.org.au, and we will be happy to help.

Links and Resources

What is NF?

Not sure what neurofibromatosis is? Watch this short video.

Join our Parents of kids with mito Facebook group

Facebook group dedicated to Parents of kids with Mito in Australia.

Event guidelines

Please follow these guidelines to ensure that all participants get the most out of Mito Foundation's online events.

Events

Mito Foundation events bring together people impacted by mito. We welcome you to join us at any of our upcoming events.