A couple whose four-year-old daughter Scarlett passed away three years ago today have raised more than £25,000 for Tŷ Hafan. In this week’s Family Friday, we find out what Tŷ Hafan meant to Chris Thomas and Clair Partridge and their precious little girl and about all the amazing fundraising they have done for us. Read More
Lyndsey Davies has a passion for fashion and is one of our amazing volunteers who support our 19 charity shops across Wales. She is also a vocal year-round advocate for sustainable fashion. Here she explains why she does what she does. Read More
Monica, one of our wonderful volunteer gardeners, explains what she and her fellow green-fingered volunteers have been up to of late, and how you may be able to help. Read More
Passionate conservationist, broadcaster and long-time supporter of Tŷ Hafan, Iolo Williams of BBC Countryfile and Springwatch took time out of filming to chat with us in Builth Wells to explain what makes him tick and why he’d love even more people across Wales to join him in supporting Tŷ Hafan. Read More
In the blazing July sunshine, we were joined by 19 teams from across Wales and beyond for a smashing day of golf, writes Hannah Barnard, Head of Operations at Principality Plastics. Read More
Dan Notley is Tŷ Hafan’s Family Support Worker for dads of children with life-limiting conditions. Here Dan, former engineer with the RAF, shares a bit about what he does, why he does it, and why he’d like you to consider Walking a Day in his Shoes. Read More
Radyr Golf Club recently hosted its annual Charity Golf Day and Vice Captain Martyn Richards shares its successes and why Tŷ Hafan is their chosen charity. Read More
Emily Harmsworth might be only 12, but she is taking on a massive fundraising challenge next month, in memory of little brother Peter, who was cared for by Tŷ Hafan. Read More
Swansea-based risk management company PCR Global is donating the profits of its Mental Health First Aid Course to Tŷ Hafan Read More
Dan Coleman from Porthcawl was a recent lucky winner of our £2,000 lottery jackpot, after receiving his ticket as a birthday gift from his mum. Read More
As the first anniversary of her death in July 2020 approaches, 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
Luca Pucella was a happy, energetic little boy with an infectious laugh, a wicked sense of humour and a tremendous zest for life. He brought love and joy to the lives of his family, his friends and everyone who knew him. But something made Luca different to other boys. He suffered from a rare, life-limiting condition, and in November 2017, when he was just eleven years old, Luca passed away. Read More
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