Support The Lauren Currie Twilight Foundation

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Support The Lauren Currie Twilight Foundation


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About this cause

About our cause

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. Join our fight against Vasculitis and help to fundraise using this site.

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Kim Cowling - 1st and 3rd Kilmacolm Guides

Kim Cowling - 1st and 3rd Kilmacolm Guides

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