Cauda Equina Champions Charity obtained charity status in 2020. Our Board of Trustees are patient led, and most importantly people living with cauda equina syndrome, their families and loved ones are at the forefront of everything we do. Using our unique insight into the patient perspective we offer bespoke services for patients through our own experiences of living with and adapting to life with CES. From our humble beginnings as a small Facebook support group of 30 members ten years ago we have grown to become the patient voice for CES patients in the UK and beyond.