Following his diagnosis Liam started coming to Little...
Duchenne Muscular Dystrophy is a rare genetic disease that causes muscle weakness and wasting. Children born with the disease have a mutation on their...
Charlotte, known to her family as ‘Lottie’, has MLD; a rare...
Children with MLD lose their ability to walk, talk, sit up, move, see and hear and eventually suffer seizures and dementia before end of life. In most cases,...
Amelia, 3 years old, from Exmouth, has been visiting Little...
Three-year-old Amelia, from Exmouth in East Devon Amelia has spina bifida and uses a wheelchair. She loves visiting Little Bridge House with mum Jemma. The...
Suzanne is 11 years old and lives with her family in...
Suzanne is the youngest of three with two sisters; Shelby 16 and Abigail 13. Suzanne’s mum Susan had a normal pregnancy and birth with Suzanne and only started...
Little Harbour supported Sarah through chemo, radiotherapy...
At 17, she was offered a referral to Little Harbour and so began, what was to become a hugely important part of our family life. Sarah juggled chemo with...
Charlton Farm supported the family through the darkest time...
Harry was born on 12 January 2004. Aged three and a half he was diagnosed with a rare bone cancer in his lower arm. Harry spent the next eight months at...