As many of you would know, my sister Giulia has a condition called Rett Syndrome.
Rett Syndrome is a progressive neurodevelopmental disorder that affects the way the brain develops. This means that Giulia is unable to communicate verbally.
On October 30th, Will and I will be going ‘speechless’ for Rett Syndrome.
We will not be talking, typing or texting for 24 hours. We are doing this to raise awareness and money for research to find a cure for Rett Syndrome and also to experience a very small degree of what it’s like to be in Giulia’s shoes for a day.
You can make a difference by donating to our Go Fund Me, which will be donated directly to The Rett Syndrome Association of Australia.
Gabriella & William
Do you want to join me in making a difference? I'm raising money in aid of Rett Syndrome Association of Australia Inc and every donation will help. Thank you in advance for your contribution to this cause that means so much to me.
More information about Rett Syndrome Association of Australia Inc: Formed in Melbourne in July 1989, the Rett Syndrome Association of Australia Inc. (RSAA) is a not-for-profit organisation which is managed by a Committee of volunteers, most of whom are parents of Rett syndrome children. The Association seeks to enhance the quality of life for persons with the syndrome and their families, and be of assistance to anyone interested in the disorder. July 2020 will mark the 31st anniversary of the Association
- Sophie Durnan
- Deirdre Lynch
- Ree Dowling
- Ted Mitchell
Fundraising team (3)
Will and Gab
Raised $2,635 from 46 donations
Rett Syndrome Association of Australia Inc
Donations are typically tax deductible in Australia.
Raised $510 from 11 donations
Raised $50 from 1 donation
This team raised $1,805 from 31 other donations.