When we were asked if we wanted to donate something for a fundraising night for Chloe Saxby, we thought the best thing to donate would be a portrait shoot to Chloe’s family. Chloe was diagnosed with Vanishing White Matter Disease in September – a rare brain disorder that has robbed her of her motor skills and slurred her speech.
In January last year she was running, jumping and dancing like any other active child, but it is expected she will be in a wheelchair within six months. There is no cure and without treatment, Chloe’s life expectancy is between five and 10 years.
We were the winners here in meeting this beautiful strong family. Our hearts go out to them xxx
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