Team Teddy

By Lucy Mort

Why we're doing it

We are running 14km in the City2Surf to raise money for Gene Therapy Research in honour of one of our littlest family members....

At 4 months old Teddy was diagnosed with an extremely rare, non-inherited genetic disease known as CTNNB1 Syndrome. This condition leads to severe impairments affecting nearly every aspect of life, including the ability to speak, walk, eat, and engage socially.

Teddy's physical and cognitive development is uncertain at this stage so it is important that we gain a better understanding of this rare condition. Research being conducted by the Children's Medical Research Institute at Westmead has the potential to make a huge impact on the lives of kids like Teddy.


By donating to Team Teddy, and supporting our runners, you will be directly contributing to ground-breaking Gene Therapy research for CTNNB1 Syndrome. 

Thank you to my Sponsors

$101.27

Chingi Dunkerley

$52.20

Grace Tague

$69

Brandon Merhab

Let's gooooo!!!!!

$10.44

Daniel Sarzano

$35

Elizabeth

Good luck reaching your goal! X

$28.19

B Dunks

$28.19

Mel And Annabelle

Go Team Teddy!!!

$20

Hannah

$52.20

Sally

$500

Jacqueline Dunkerley

$52.20

Clara Pollock

$500

Peter Mort

$104.40

Dominique De Vries

$208.80

Lr&p

$208.80

Jcnh

$104.40

Jim Huckerby

$208.80

Carolyn Foxton

$208.80

Michele Armstrong

$104.40

M And L Holford

$38.63

Rashmi Ghimire

$50

Adrian Brezniak

$78.30

Anonymous

$20.88

Ellen De Vries