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 Read stories patients and their families have shared with us about their journey.  Soarin...
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When I first heard about Camp Footloose to be honest I was a bit hesitant and didn’t really want to go, and as it turns out, choosing to go was one of the best decisions of my life.I met kids just lik...
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My name is Caitlin Holder and I suffer from Systemic Arthritis which impacts my everyday life. School was difficult to manage at times, as it took time to learn what I was capable of.With manage...
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Our son was diagnosed at a time when we were just learning about being parents, and suddenly had to learn about a disease affecting our baby boy. We were overwhelmed and under-informed.It hasn’t been ...
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2017 started for us on a high, everything was falling into place – our swimming pool was due for completion, kids’ sports organised, last minute fundraising for the trip of a lifetime with kids dance ...
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Hi, my name is Alicia. My daughter Georgia was diagnosed at 17 months old with Chronic recurrent multifocal osteomyelitis, or CRMO for short.Georgia began her life as a very healthy baby however in No...
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All grown up and moving to adult healthcare services? We've linked the ACI transition care network below and 'Trapeze', our program for hospital patients.   ...
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On this page Contact details The Children’s Hospital at Westmea...