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In 2011, after several years of misdiagnosis of aches and pains as gout or repetitive strain injury, Malcolm was diagnosed with a rare form of Systemic Vasculitis - non ANCA Microscopic Polyangiitis - affecting the peripheral nervous system. Malcolm is in remission now.

Having no previous knowledge of Vasculitis, The Lauren Currie Twilight Foundation was there to enlighten, help and support. It's our turn now to help LCTF continue their wonderful work.

Malcolm and I will be walking/running/hopping/skipping the annual LCTF 5k in Bellahouston Park. Please help us raise money for LCTF to help them support Vasculitis through funded research, drug trials and specialised patient support services.