Ride for Chloe kicks off on Sunday to raise funds for a cure

LW
Updated October 14 2017 - 9:09am, first published October 13 2017 - 6:00pm
Rough ride: Grant Saxby with his daughter Chloe who is one of seven Australians with the rare Vanishing White Matter disease. He is leading a ride from Melbourne to Wollongong to raise funds for research. Picture: Adam McLean
Rough ride: Grant Saxby with his daughter Chloe who is one of seven Australians with the rare Vanishing White Matter disease. He is leading a ride from Melbourne to Wollongong to raise funds for research. Picture: Adam McLean

Chloe Saxby has struggled for six years with a degenerative brain disease, but thanks to her family’s efforts a cure may be on the horizon.

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LW

Lisa Wachsmuth

Deputy Editor

Deputy editor and health reporter at the Illawarra Mercury, covering stories in the Wollongong, Shellharbour and Kiama local government areas. For news tips email lwachsmuth@austcommunitymedia.com.au

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