It was an absolute honour to speak at the Saving Chloe Saxby charity ball last night.
Chloe has Vanishing White Matter Disease, one of the rarest diseases in the world. She needs support.
As a father I have no words to describe how I would feel if something happened to my little princess. Chloe's and her beautiful parents are an inspiration.
A big shout out to all the people who dug deep...
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