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This February we will be walking to raise both funds and awareness for Cystic Fibrosis.
Harriet was diagnosed with CF at 5 weeks, over the last 8 months we have come to learn a huge amount about the genetic mutation and it's effects on the body, specifically our little girls body.
While Harriets journey has barely begun we are lucky to be living in an era where new treatments are being regularly discovered and we are supported every step of the way. The awareness and fundraising from events such as this will help ensure that Harriet and others living with CF will go on to lead long, full and healthy lives.
The support we have received from family, friends, colleagues, her health team at Westmead Children's Hospital and the community has been nothing short of amazing - thank you.
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