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Stanley Murphy

Stanley’s story

Stanley had Tay Sachs disease and died in his Mum's...
When four-year-old Stanley sadly died in his mum Emma's arms at Little Bridge House in June 2019, the love, kindness and support the family received from the...
Liam Jones with mum Natalie

Liam's story

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

Charlotte's story

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

Amelia’s story

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 Clemens

Suzanne's Story

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...
Sarah Gibb

Sarah's Story

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...