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Tayen's lockdown story

Eight-year-old Tayen and her family have been shielding at...

Since lockdown began, Tayen and her family have been shielding at home to ensure that she can continue to have her chemotherapy treatment as safely as possible...
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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...
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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...
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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...
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Suzanne's Story

Suzanne is 11 years old and lives with her family in Redruth...

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...
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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...
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