Layla's Trust seeks to provide support for bereaved families who have lost children and to families who have disabled or terminally ill children.
The organisation was set up in memory of baby Layla Mae Cotter, who died aged 70 days old in February 2011. She suffered from a rare genetic condition called Gaucher Disease Type 2 and spent most of her short life in St. Mary's hospital, on the Isle of Wight.
Layla Mae will live on in all our memories and be remembered through the work Layla's Trust will offer sick children and their families. She will never be forgotten.