Our local shops raise vital funds to help us provide unique care and support to life-limited children, young people and their families.
More about our shopsChoose from a selection of caring gifts, from just £10, that will enable life-limited children, young people and their families make the most of the time they have together.
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Want to challenge yourself and do something you never thought you could? Then why not have a browse at the running events that are happening near you!
Want to challenge yourself and do something you never thought you could? Then why not have a browse at the running events that are happening near you!
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“For us, Tŷ Hafan is a total lifeline” says Sophie, Ollie's mum. You can be a lifeline too for families like Ollie’s by including a gift in your will for Tŷ Hafan.
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The Tŷ Hafan All Stars ice hockey team have raised a phenomenal £60,000 since they started supporting our charity in 2016. Read More
Our fantastic supporters at London Welsh Rugby Club collectively travelled more than 2,000km to raise £6,000 for Tŷ Hafan. Here the club’s Damian McCarthy tells all. Read More
Andrew Evans was over the moon when his first child Oscar was born in 2011. But happiness turned to heartache when his beloved baby boy was diagnosed with a life-shortening condition at just nine months old. Read More
Seventy staff from the King’s InterHigh international online school recently spent the weekend at the Glastonbury Festival fundraising for Tŷ Hafan, donating their volunteer fees for helping at the festival campsites. Read More
Seth Burke, 13, is Member of the Welsh Youth Parliament for Tŷ Hafan and represents the voices of children from our hospice as well as those of children supported by Tŷ Gobaith children’s hospice in North Wales. Last week he attended this Welsh Youth Parliament’s first in-person meeting since the start of the pandemic. Here is Seth’s take on the day. Read More
Last week we spoke to Matt Evans, one of a group of Tŷ Hafan fathers and friends who are, as we write now, in the middle of an immense physical and mental challenge in a bid to raise £50,000 for Tŷ Hafan. Read More
“We’ll be suffering for 55 hours, our children go through so much more”. Tŷ Hafan dad Matt shares his thoughts on the 10nTaff Read More
A team of Principality employees decided to lace up their hiking boots, and sign up for the welsh3peaks challenge for Tŷ Hafan Read More
This week’s blog is from Gareth, who along with his friend James have truly gone the distance to support Tŷ Hafan where Gareth's partner, Nicola, works as a nurse. Read More
Q: What do a former Wales rugby captain, a BBC Wales Scrum V analyst, a major Welsh plastics business and dozens of keen golfers have in common? A: The first Tŷ Hafan Great Days Golf fundraising charity event! Read More
“So much has happened in my life with Cai. When he was little he was diagnosed with the ultra-rare Vici Syndrome and even though he has died I take a lot of comfort from the way it happened and how it happened. Read More
Beverley shares her late daughter’s story, and how Tŷ Hafan helped Jalene to have the best life, and death, possible. Read More
Sophie and Sean were just 22 when their little son Ollie was diagnosed with the ultra-rare MOSAIC Syndrome. Here Sophie shares their story and explains how Tŷ Hafan is, quite literally, a lifeline for the whole family. Read More
Jaiden, 14, has counselling and music therapy with Tŷ Hafan and all from the comfort of his own home in Llandrindod Wells. Here, he and mum, Anne-Marie, share their story and explain what Tŷ Hafan means to them. Read More
My name is Sarah and I am Mum of two beautiful girls Molly and Emily who both have Rett syndrome. Read More
Harley, a “cheeky chops” seven-year-old from Llanelli, is definitely one of a kind. He had his first operation on a cystic lung when he was still inside his mum Becca’s tummy and at two days old, he had open surgery to remove most of his left lung. Read More
Just hours after Osian Liddlell was born, his parents' joy turned to fear, as their precious baby boy was transferred to the neo natal intensive care unit. A rash had spread across his face and body and doctors immediately started carrying out tests to find out why. Read More
When baby Riley came into the world 7 years ago, his parents couldn't wait for him to meet his three older brothers. But as soon as Riley was born, his parents knew something wasn't quite right. Read More
Sisters Molly and Emily bring so much joy and love to their mum and dad's lives, but since they were born, life is not how their parents James and Sarah ever expected it to be. Both girls were born healthy babies two years apart but as time went on, their parents noticed their daughters weren't developing as they should be. Read More
Doctors diagnosed Lilly-May with Leukodystrophy, a life-limiting brain condition that affects the central nervous system, which is responsible for nearly everything we do from our heartbeats to walking. Read More
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