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The Lauren Currie Twilight Foundation was set up in the memory of Lauren Currie who died of Wegener's Granulomatosis (rare variant of Vasculitis) on 23rd October 2010 - aged 15. Vasculitis is an auto-immune disease affecting the body's vascular system and affecting major organs.
The Foundation is dedicated to funding Vasculitis research and UK awareness. Wegener's Granulomatosis is a rare variant of Vasculitis with no known cause or cure - only immune suppressive treatments. It is important more funds are dedicated to research and awareness is heightened for early diagnosis.
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Kim Cowling - 1st and 3rd Kilmacolm Guides
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