Company director of 15+ years. Founder of FOP Friends a charity for FOP (my son Oliver's condition). Board member of IFOPA. Manchester 829 Round Table chair.
💙 We're lighting up the town hall tonight for #RareDiseaseDay and the 300 million people worldwide living with rare diseases.
Oliver, pictured with @CatherineLHynes, lives with fibrodysplasia ossificans progressiva (FOP), a rare genetic disorder.
Info: https://t.co/AtjTaZbUrT