Xander support

Melissa Williamson of Bona Vista has been overwhelmed by community support for her two-year-old son Xander after his diagnosis with rare genetic syndrome Pitt Hopkins.  With an innovative therapy, the family hope Xander can soon enjoy the simple things other kids take for granted.

At first glance Xander Williamson is just like any other two-year-old boy with his cheeky smile, bright blue eyes and a mop of blonde hair. However, Xander is rare.  So rare that he is only the 11th Australian diagnosed with

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