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 this event.
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
Meet your hosts
Preeti Raghwani |
Diane Cass |
Ruth Lindsay |
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.
Not sure what neurofibromatosis is? Watch this short video.
Join our dedicated Facebook group for mito parents: Parents of kids with Mito Australia.