Indi’s SMS journey

06/08/2025

I am off to zone athletics for the 100m and 200m so excited for this, going to show everyone how I can do this.

11/02/2025

Tonight I helped make my lunch for school we made star and hearts shape sandwiches.

11/02/2025

New website check it out ❤️

🚀 Exciting news! We have just launched our brand-new website! 🎉

Visit www.smsaustralia.org to explore resources, support, and community connections for individuals and families impacted by SMS, particularly those living in Australia.

Check it out and help us spread the word! 💙

Prisms, Inc.

05/02/2025

School holidays are over just like that we are in year 2
You go shine and show them everything my little shining star.

13/12/2024

I have been working so hard to be able to have the confident to stand in front of people and this week I done it with the school talent show. Everyone is so proud of me.

18/11/2024

Me and my siblings celebrating SMS day ❤️❤️

12/11/2024

Over the weekend I went to my SMS Camp, got to see my friends again and do lots of fun activities and try new things

05/11/2024

Been so busy at school, I am in the aboriginal dance group and I love learning them

05/11/2024

Some fact about me

Well SMS.

SMS Awareness Day is 17th November and in honour of SMS Awareness Day, we are sharing facts throughout this month about Smith-Magenis Syndrome.

The diagnosis of Smith-Magenis Syndrome is usually confirmed through a clinical blood test called a chromosome microarray analysis (CMA). Diagnosis can also be made through a cytogenetic test called FISH (fluorescence in situ hybridisation). These tests can detect the deletion on the 17th pair of chromosomes that is the most common cause of SMS.
In cases where a deletion is not detected, next generation sequencing tests can be used to detect changes in the RAI1 gene.

Learn more and join in by visiting https://www.prisms.org or https://smsaustralia.org.

24/05/2024

Been working so hard on swimming lessons and it’s finally working