Ty Hafan

#familyfriday

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Elain

"marathon in may - a great way to focus on something positive "

Aberystwyth-based Bridget and her daughter Elain, share their experiences tackling, and succeeding to complete last year’s Marathon in May. Read More

Connah and friends fundraising

"st david’s day celebrations in kabul"

LCpl Connah Bason, who is originally from Llanelli, is currently deployed in Kabul. He celebrated St David’s Day very differently this year and all in aid of Tŷ Hafan. Read More

Esmai Roddy

"“tŷ hafan is the only respite that me and esmai get”"

Four-year-old Esmai was diagnosed with CHARGE Syndrome shortly after she was born and has been using Tŷ Hafan's services since 2017.  Read More

Tricia Jones underneath the finish line banner her husband, Ian, made to celebrate her efforts

"walking 2,000 miles for tŷ hafan during lockdown"

Tricia Jones completes her very own 2,000 mile odyssey to help keep fundraising for Tŷ Hafan through lockdown. Read More

phae jones headshot

"a whole other layer of empathy"

Phae took a few minutes out of her busy schedule to share with us why she wanted to work for Tŷ Hafan and what she hopes to achieve in her new role. Read More

karen's decorations

"letting the light shine"

Karen decorated a Winter Wonderland for Karen&rsquo;s children. With each passing year, people started to stop by her house to enjoy her lights. Read More

kate

"we would walk....170 miles "

The team at Taylor & Co has found a way to get back to fundraising for Tŷ Hafan while staying safe. Read More

circle

"going full circle"

Circle's challenge will take them around the circumference of the Earth, 40,075km...virtually...to raise money for Tŷ Hafan. Read More

elain

"get fit with mother and daughter team this half term"

Hear how ‘Team ApelElain’ has helped to raise over £40,000 and counting for Tŷ Hafan! Read More

Ride to the Rugby

"Tŷ Hafan Dad cycles to Paris again… virtually this time"

Tŷ Hafan Dad's experience of cycling to Paris and Dublin during our Ride to the Rugby events and this year's virtual event. Read More

straeon teuluoedd

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harley and becca

harley's story

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

osian

osian's story

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

riley

riley's story

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

Molly and Emily

molly and emily's story

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

Lilly-May

lilly-may's story

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

luca's story

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

Felix

felix's story

When Dan and Alex's baby son Felix was just a few months old, his parents received the devastating news that their little boy had a life-limiting condition and would never walk, talk or even live past infancy. Read More

Cai

cai's story

Even though Micaela knew she had a high risk pregnancy, she and her partner Matthew had no idea about just how poorly their little boy was going to be. Read More

elain

elain's story

Elain James was referred to Tyˆ Hafan in January 2011 when she was just 8 months old. Elain was antenatally diagnosed with congenital heart disease, but it wasn’t until she was born that her family knew the full extent of her illness. Tests revealed Elain had multiple, complicated heart conditions and a rare genetic disorder called 22q11.2 Deletion Syndrome. She also has a permanent feeding tube attached to her stomach. Read More

alice

alice's story

When Alice was born at 34 weeks, the doctors delivered devastating news to her mum and dad – their newborn baby girl had just 20 minutes to live. Barry and Rebecca had known their daughter was at risk since their 20-week scan had picked up problems, with serious implications for their unborn baby’s safety. But they could never have imagined the difficult road that lay ahead of them. Read More

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