top of page
News


Speechless Ambassador: Te Buda
Meet Te Buda, our first Speechless Ambassador for 2022. Te has registered to go speechless for Rett Syndrome for 24 hours again this...
maryepritchard
Oct 15, 20221 min read
33
0


Speechless Teachers?!
Welcome to our 2022 Speechless campaign. This year we are kicking off with some amazing insight from 2 dedicated educators - Jenni and...
maryepritchard
Aug 29, 20224 min read
31
0


It was an amazing opportunity experience what my daughter faces day to day
Brett, NSW, 24 hours speechless How has your life been touched by Rett Syndrome? My beautiful daughter Holly was diagnosed 5 years ago...
maryepritchard
Oct 27, 20212 min read
354
0


Seen it. Loved it. Got the T-Shirt?!
Show your support and spread awareness, all while looking super stylish in one of our fabulous speechless t-shirts. Made to order,...
maryepritchard
Oct 26, 20211 min read
50
0


My dream is that in the near future I can tell families about a cure for Rett Syndrome
Speechless for Rett Syndrome would like to introduce you to Dr Carolyn Ellaway. Dr Ellaway has been working with Rett Syndrome for over...
maryepritchard
Oct 24, 20212 min read
949
0


People sometimes forget to include you because you are not speaking
Jan, NSW, 24 hours speechless How has your life been touched by Rett Syndrome? I work as an SLSO in a public school in NSW. This year I...
maryepritchard
Oct 23, 20212 min read
58
0


"It is our duty as medical researchers to find a cure"
Speechless for Rett Syndrome would like to introduce you to Dr. Wendy Gold. Dr. Gold has been studying Rett syndrome for the past 10...
maryepritchard
Oct 20, 20212 min read
55
0


Remember this is not a game - people are going through this everyday
Oscar, aged 9, ACT, 24 hours speechless Oscar (and his Mum and Dad) decided to go speechless for his best friend, Abigail, who has Rett...
maryepritchard
Oct 17, 20211 min read
22
0


I hope those facing Rett see there is an amazing community of people who are all on their team
Angela, ACT, 24 hours speechless. Angela reflects on her Speechless experience, and what she learnt from it. I liked learning Abigail’s...
maryepritchard
Oct 17, 20213 min read
13
0


Canberra Family goes Speechless to cure Rett Syndrome
All is quiet in the Dow family home today as Oscar (aged 9) and his parents Susan and Mark all take on the Speechless challenge together...
maryepritchard
Oct 10, 20211 min read
45
0


If I do the challenge again I won't be watching the Wallabies...!
Derek, Victoria, 12 hours Speechless Derek shares his experience of stepping up tot the Speechless for Rett Syndrome challenge! How has...
maryepritchard
Oct 5, 20212 min read
43
0


I've always dreamt of the day I hear my sister's real voice
Te is 13 years old and big sister to Annelise, aged 11 who has Rett Syndrome. She is taking on the 24 hour Speechless for Rett Syndrome...
maryepritchard
Oct 3, 20211 min read
113
0
bottom of page