Dedicated to the memory of Yvonne Williams

Our beautiful mum lived and battled with PSP for six years of her life before we lost her on the 9th of June 2016. As PSP is such a rare and unknown condition, any donations will go a long way to helping fund research into treatments or possible cures in the future for this terrible condition. Mum was a strong and brave lady and always kept her ability to smile and laugh, but PSP still robbed her of so much more. With love and thanks, Yvonne's family xx 

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