At 11 days old, Rowan was diagnosed with Wolf-Hirschhorn syndrome (WHS), a rare genetic disorder that causes delayed growth and development in many parts of the body.
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Let’s break that down a bit.
It seems daunting, but these stats aren’t permanent. We’re changing the outcomes, because every kid deserves a childhood.
Here’s how we’re doing it:
Your contributions support researchers who uncover new cures and gentler treatments through ground-breaking research and clinical trials.
Your support helps deliver the best care possible at every touchpoint, including frontline paediatric training and education, as well as new partnerships, technologies and healthcare delivery models, telemedicine, and satellite centres for community health.
Your donations support therapies, spaces and equipment that are designed for the specific needs of children and youth, such as child-centred and youth-oriented programs, family-centred facility design, and adaptable equipment and technology.
Thanks to your support, we’re helping hospitals change the outcome for sick children. But the fight isn’t over. And we need you now more than ever. Get involved.
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