STEVE WAUGH FOUNDATION AUSTRALIA
WHO WE HELP

WE WILL SUPPORT AND ASSIST CHILDREN & FAMILIES AFFECTED BY A RARE DISEASE THROUGH:

• Providing or supporting medicine


•  Providing or supporting equipment


•  Providing or supporting treatment & therapies



 

Elisabeth – Freedom to move

Elisabeth is a delightful little girl born with an extremely rare condition called Jeune Thoracic Dystrophy.

   

This condition means she has a small thoracic cage which stops her lungs from growing and is completely dependent on a ventilator to breath. Elisabeth has spent almost all her life in hospital. Her family and medical specialists are working hard to support her high dependency needs at home and in the community to bring some sense of normality to her life. Her illness and prolonged hospitalisation have impacted Elisabeth’s development. She is unable to participate in regular activities with her friends and reaching milestones such as walking is a real challenge.

Thanks to our generous supporters, the Steve Waugh Foundation has been able to provide a custom-designed tricycle to help Elisabeth with her physical development and give her some mobility and freedom. It has been designed for Elisabeth’s short stature and can be adapted by physiotherapists as she grows. Through the combined efforts of her family, carers and hospital staff, Elisabeth has made great strides in her development, is interacting with others, and is now at last equipped to break free of the hospital to play in the surrounding playgrounds and gardens.

Through the combined efforts of her family, carers and hospital staff, Elisabeth has made great strides in her development, is interacting with others, and is now at last equipped to break free of the hospital to play in the surrounding playgrounds and gardens. ped to break free of the hospital to play in the surrounding playgrounds and gardens.

 

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