This site is dedicated to the memory of Nikki.

My daughter was and is still a massive part of my life. She made me laugh, she made me cry but above all she made me very very proud. I miss her dearly every single day. She was the funniest girl I knew and always seemed to know just what to say to make me smile. Such a rare and unique character that could never be replaced xx

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Cystic Fibrosis Trust
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