Celebrating 20 Years of the Steve Waugh Foundation: A Legacy of Strength and Support

 
 
 

The Legacy

Since 2005, the Steve Waugh Foundation has been a beacon of hope for young Australians living with rare diseases. Founded by Steve Waugh after his retirement from international cricket, the Foundation was built on the belief in “strength of character” and a commitment to supporting children, young adults and their families facing extraordinary challenges. With more than 2 million Australians living with a rare disease—400,000 of them children—the need for specialised support has never been greater. For two decades, the Foundation has proudly been ‘somewhere to turn,’ delivering vital assistance and funding to those who need it most.

The Journey

At the heart of The Bayard Foundation lies the need to carry the load by highlighting programs in need of funding, showing compassion, making connections, and helping make a difference. So our decision to back this fantastic charity was only natural. After attending many years of the annual golf Grange Forever Green event and pledging support we are proud to see the results of this wonderful foundations work.

Last year was the foundation's 20 year anniversary- it was a massive milestone to celebrate the work that they do. Our co founder Kerry-Anne and Patron of SWF participated in the ladies winning team of the golf day. 

Honouring Two Decades of Dedication and Hope

The SWF Grants Program relies entirely on the support of one-time donors, major sponsors, volunteers and patrons who share our mission to champion children with rare diseases. The Bayard Foundation are proud supporters of this cause; as it truly embodied the spirit of strength and resilience, enabling life-changing outcomes for young people across the country. At this event we were able to celebrate 20 remarkable years of impact, it hit close to our hearts and we were proud to donate a major contribution to keep this vital work to continue. Together, we are helping to build a more compassionate future for children and families affected by rare diseases across Australia.

 
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Ro’s morning tea