

Freya’s story
Two-year-old Freya is her mum’s ‘little bestie’. She’s ‘super sassy’, loves cuddles and enjoys listening to stories at bedtime. She also hates water and…
Read the storyEvery family’s experience is different. These stories share how Acorns provides specialist care, comfort and support to children with short lives and the people who love them.


Two-year-old Freya is her mum’s ‘little bestie’. She’s ‘super sassy’, loves cuddles and enjoys listening to stories at bedtime. She also hates water and…
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“Acorns was everything we needed without knowing we needed it.” Mum Karen tells the heart-breaking story of their daughter Thea.
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‘Hannah knew she was terminally ill and that she was going to die. That is horrible for anyone of any age, especially a teenager.’…
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16 year old Jack had cerebral palsy and visited Acorns for the Three Counties, our children’s hospice in Worcester. Sadly, in November 2020, he passed away.…
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Grayson was a beautiful baby, with deep blue eyes and a perfect smile. For mom Becky and dad George, he was their ‘little miracle’.…
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If you ask eight-year-old Vinnie about his condition, he’ll tell you he was born with half a heart and that one day he’ll need…
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Mum Liga shares her powerful story and explains why there’s no-one else who can offer this vital support. She reveals how Acorns and the…
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It was the darkest time of their lives, but with the help of Acorns, Tony and Zoe Atzori created a lifetime of memories with…
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“Yusuf is a little cutie pie,” says mum Iram. She’s right. His big beaming smile greats everyone who meets him. Yusuf is one of…
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Mum Sam Barklam reveals how support from Acorns helps local families like hers. “I’ll never forget that first visit from Acorns, it was just…
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Being a first-time mum can be daunting for any parent, but when Sarah’s son Ethan suffered a catastrophic stroke during delivery her world changed…
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Bluebell was born with exomphalos major, meaning some of her organs were on the outside of her body. At Acorns, we are here to…
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Cara has a condition called nonketotic hyperglycinemia or NKH for short. It is a rare genetic condition which prevents her body from processing glycine…
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Karvarli is a social butterfly. He loves to be around people, spreading smiles and stealing hearts wherever he goes.
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Patrick, now aged two, suffered a brain injury when he was born suddenly and unexpectedly at home. In the space of a few hours,…
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Harry and George both have a rare genetic condition. It’s so rare that there are only around 100 cases in the world.
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Just weeks old, Oliver was diagnosed with stage five chronic kidney disease, a life threatening condition that meant his kidneys were close to failure…
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Meet Ezra – a little boy with one of the biggest smiles. But behind that beaming smile and magnetic personality is a little boy…
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