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When MPS keeps pushing me down – I just keep moving

Thursday 01, Feb 2018

To celebrate Rare Disease Day 2018 (28 February), the MPS Society Australia joined forces with the Sydney Dance Company to put on a dance class – with a difference.

On Friday 9 February 2018, two of our MPS members and their families visited the Sydney Dance Company studios and participated in a workshop with the Company’s Pre-Professional Year dancers. 

15-year-old Tabitha Ellem from Canberra and 8-year-old Isabelle Schodde from Ipswich spent the day at the Sydney Dance Company and showed how they never let MPS hold them back…they just keep dancing! 

Be sure to show your support for MPS this Rare Disease Day by liking or sharing this video among your personal networks – use the hashtags #ShowYourRare #ShowYouCare #KeepDancing #SDCStudios to join the conversation. 

This special initiative was proudly supported by Sanofi Genzyme.