Noah's Ark Children's Hospital Charity

Noah's Ark Children's Hospital Charity Raising funds to ensure that Noah’s Ark Children’s Hospital for Wales has the best resources avail We’re here to help and we’d love to hear from you.
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The Noah’s Ark Children’s Hospital Charity is the official charity for the Noah’s Ark Children’s Hospital for Wales. Having raised more than £22 million to build and equip the now fully operational Noah’s Ark Children’s Hospital for Wales, today we continue to work hand in hand with the NHS, providing funding for the most up to date equipment and facilities. We also fund support services for famil

ies like the play specialist team, who help children be children, despite the difficulties they are facing. By donating or fundraising on our behalf, you are playing a part in supporting the 73,000 children who receive specialist and life-saving treatment at the Noah's Ark Children's Hospital for Wales each year. Some of them only stay for an hour, others are patients here for their whole childhood, but you are helping to make a difference to each and every one of them. Whether its running a marathon, holding a bake off, making a monthly donation or leaving a gift in your will, there are hundreds of ways to get involved in our work. You can support us as an individual, as part of a local group or through your business. Our website is full of ideas so you’re bound to find something that suits you. Visit www.noahsarkcharity.org or give us a call on 029 2184 7310.

For four-year-old Hallie, blood tests have been a part of her life since day one.  It doesn’t make the experience any le...
21/08/2026

For four-year-old Hallie, blood tests have been a part of her life since day one. It doesn’t make the experience any less daunting, but thanks to a new venepuncture chair funded by people like you, things are looking up.

Hallie was diagnosed with epilepsy and tuberous sclerosis complex type 2 (TSC2) when she was two months old. It’s a rare genetic condition that causes non-cancerous tumours to grow in different parts of the body, causing seizures. She also has a very rare condition called primary intestinal lymphangiectasia, which affects the lymphatic vessels in the intestine. Together, her conditions mean Hallie has spent a lot of time in hospital and is cared for by a multidisciplinary team at Noah’s Ark, including gastroenterology, neurology, dietetics and immunology.

Hallie initially needed blood tests on a weekly basis. Nowadays, they’re every three months alongside her regular treatment and monitoring, but that hasn’t always made it easy for Hallie, who’s now older and more aware. Mum, Louise, explains: “Hallie is the most confident person talking to doctors and nurses. She likes to get involved, but she has a lot of medical anxiety from being poked and prodded from such a young age .The old venepuncture chair was a bit rickety and that also added to her anxiety.”

Over the years, Louise has found ways to help Hallie prepare for procedures, playing at practising with medical equipment at home. She says the play specialists have also been a great help and because the whole team know her so well, they make sure everything Hallie needs is ready before they begin.

But the venepuncture chair has been the missing piece of the puzzle for Hallie. It’s larger than the one she needed to use before. It can recline and, importantly for a little person like Hallie, it’s big enough for her to sit safely and comfortably on her mum’s lap. It gives her the physical support she needs while allowing Louise to sit with her, hold her arm and provide the comfort only a parent can.

Louise said: “She’ll only sit with me. Having the space for her to sit on my lap makes such a difference.”

The team on outpatients are also seeing the benefits, reporting that the new chair allows blood draws to be carried out more quickly and efficiently, helping to reduce the number of attempts that some children need. This is great news, particularly when you consider that this type of procedure is carried out on around 30 patients every day.

A chair might seem like a small thing. But for a child like Hallie, and for the thousands of other children who’ll use it each year, it will make a very real difference.

This is what your donations help fund. Your support gives families the equipment, comfort and specialist support they need to make difficult moments a little easier, allowing parents to be there, close to their child, when they need it.

And for Hallie, there is some wonderful news. She has now been seizure-free for a whole year for the first time ever. She continues to have regular MRI scans and ultrasounds to monitor the tumours, while medication is helping to keep her stable.

Come and join us at Chepstow Racecourse’s Family Fun DayWe’re delighted to reach out and share a new opportunity that we...
21/08/2026

Come and join us at Chepstow Racecourse’s Family Fun Day

We’re delighted to reach out and share a new opportunity that we’d love for you and your family to be part of!

Come and join us at Chepstow Racecourse’s Family Fun Day this bank holiday Monday!

We’re looking for volunteers to help run our activity stall and raise awareness for the Noah's Ark Charity.

Chepstow Races Family Fun Day
Monday 31st August
Time: 11am to 6pm
Location: Gate 4, Chepstow Racecourse, Chepstow, Monmouthshire, NP16 6EH

Volunteer duties may include:
✨Bucket collection
🎨 Providing glitter tattoos to families
🎪Assisting with arts, crafts and games

What we provide:
- A Noah’s Ark t-shirt to wear on the day (and keep!)
- Water and snacks
- Travel expenses to cover your return journey (public transport or mileage)
- The chance to earn Tempo Time Credits - meaning you can earn credits every time you volunteer, and exchange them for exciting rewards like theatre and cinema tickets, sporting events, gym passes and more!

Your support makes a huge difference, and we’d love to have you with us!

If you'd like to get involved, please email [email protected]

Pizza Thursdays! 🍕Being in hospital can be tough, particularly during the school break when everyone else seems to be ha...
18/08/2026

Pizza Thursdays! 🍕

Being in hospital can be tough, particularly during the school break when everyone else seems to be having plenty of treats and fun. Though we can’t make everything better, we can do the little things that add up to make a difference to people’s day. So every Thursdays during the summer holidays, our sparkle team have been distributing pizzas to children and families on the wards.

Made by Fizz n Flour, these weekly deliveries are a chance for families to enjoy a summer treat together in a way that feels normal and familiar.

It’s all been made possible thanks to charity supporter, Martienus Thomas who raised funds by walking from Aberaeron to Noah's Ark raising an incredible £5,670.78. The money was used to provide hot meals for families who spent Christmas Day in hospital as well as Pizza Thursdays! It was an idea rooted in lived experience for Lewis' and his family who know how much a warm meal can mean when spending time in hospital.

Today, on International Youth Day, we’re delighted to introduce our newest charity youth ambassador, 15-year-old Sienna....
12/08/2026

Today, on International Youth Day, we’re delighted to introduce our newest charity youth ambassador, 15-year-old Sienna.

Sienna, from Cardiff is passionate about raising awareness around Type 1 diabetes. Having lived with the condition since she was 10, Sienna knows first-hand how important understanding and support can be. Here, in her own words, is her story:

Hi, I’m Sienna.

This September will mark five years since I was diagnosed with Type 1 diabetes so I’ve decided to share my story because I want other people with it to know that you are never alone, and it’s okay not to have all the answers.

Before I was diagnosed, I remember going to the toilet much more often, drinking a lot more water and losing a lot of weight very quickly. I didn’t understand what was happening to me.

The night I went into hospital is something I remember very clearly. I felt incredibly unwell and told my mum, “There’s something wrong. I can’t breathe properly.”

We went straight to A&E.

My mum told the triage nurse that she suspected I had diabetes. She didn’t really know anything about diabetes, but just weeks before, something she had heard stayed in her mind, and she trusted her instinct that something wasn’t right.

A finger-prick blood test showed my blood sugar was in the 30s. Suddenly, everything became much more urgent.

After I came home, I had so much to learn, understanding what my body needed. Going back to school was difficult too. I heard comments and misconceptions, and eventually I decided to hide my Type 1 diabetes.

For years, I didn’t want anyone to know. But now, as I go into Year 11, I am done hiding. I’m proud to say that I have Type 1 diabetes, and I’m not hiding it anymore.

Knowing the symptoms can save lives. I’m sharing my story because I know what it feels like to be 10 years old, frightened, and suddenly expected to understand something that will affect you for the rest of your life.

Type 1 diabetes does not define who you are. And it’s okay not to have all the answers. You’re still learning. Just like I am.

Read Sienna’s full story here: https://noahsarkcharity.org/patients/siennas-story/

We're looking for a dynamic marketing manager to lead campaigns that grow our impact, boost awareness, and drive fundrai...
10/08/2026

We're looking for a dynamic marketing manager to lead campaigns that grow our impact, boost awareness, and drive fundraising - all in support of children and families across Wales.
This is a hands-on, strategic role, working alongside fundraising and service delivery teams to strengthen our reputation and expand our reach.

If you're a communications professional with an impressive track record and a passion for making a difference, we want to hear from you.

Apply now and help us create brighter todays and better tomorrows for the children and young people of Wales.

https://noahsarkcharity.org/2026/08/10/marketing-manager/

A few weeks ago, some of our Noah’s Ark families were able to swap hospital appointments and wards for a day of musicand...
08/08/2026

A few weeks ago, some of our Noah’s Ark families were able to swap hospital appointments and wards for a day of musicand fun in the sunshine at the annual GlastonBarry event – all thanks to its generous organisers who donated tickets.
 
The festival gave families the chance to just enjoy being together, while meeting otherchildren, parents and siblings with similar experiences. It was an opportunity to share stories, ask for advice and build bonds. 
 
10-year-old Lilah who spent six months in hospital after becoming seriously ill last summer, went along with her mum and siblings. Mum, Lyndsey said: “We had an amazing time. It was a much-needed day of fun after such a difficult year, with Lilah spending so long in hospital.

“My son Ronnie absolutely loved the wrestling show, while Lilah and Elsie really enjoyed all of the music. The food was fantastic, and everyone had a brilliant time on the funfair rides.

“The best part was being able to enjoy a normal family day together. Since Lilah became a wheelchair user, we’ve found that some activities can be quite limiting, but GlastonBarrywas so inclusive that she was able to join in and have an incredible time. She danced the day away with the biggest smile on her face, and seeing her so phappy made the day even more special.”

“Thank you to everyone at Noah’s Ark and everyone else involved in making it such a wonderful event and for giving our family memories we’ll treasure. We are very grateful.”

 
A huge thank you to GlastonBarry for gifting the tickets and making this special day possible for the families we support. Your generosity helped create a lot of fun filled Summer 2026 memories.

Kirsten from Swansea is an experienced mum of five. Having had fairly straightforward pregnancies and births with her ot...
06/08/2026

Kirsten from Swansea is an experienced mum of five. Having had fairly straightforward pregnancies and births with her other children, she’d been anticipating something similar for her fifth pregnancy. But this time things were very different.

Kirsten was pregnant with identical with twins. Early on in the pregnancy, she was diagnosed with twin to twin transfusion syndrome, a rare but serious condition where uneven blood vessel connections cause one twin to lose blood to the other. The babies were monitored closely but tragically, at an 18 week scan, it was discovered that little Blossom had died.

At 24 weeks, Kirsten an husband Dan, feared that they may be about to lose their second twin, when Kirsten’s waters broke. She was rushed to Southmead Hospital, the closest place at the time with an available NICU cot, but thankfully the labour didn’t progress.

Just before Kirsten was due to be induced at 36 weeks, baby Olive decided to time her own entrance. Because there were some concerns about some swelling on her bowel, Olive was taken to NICU to be monitored. Things looked to be going well at first, but as her feeds were increased, Olive began to struggle. She seemed unable to keep down anything over 16 millilitres of milk. At two and half weeks old, the decision was made to take Olive down for exploratory surgery, where the cause of the issue was discovered. Olive had an Ileal atresia, a congenital birth defect where the lower part of the small intestine is narrowed or blocked. It was a diagnosis that baffled the NICU team, as Olive had been passing the food she’d been able to take, which is highly unusual in cases like these.

Olive had 20cm of her small intestine removed, returning to NICU sedated and ventilated. For Kirsten and Dan, who had already been through so much, it was a hugely difficult thing to see.

It was around this time that Olive and Kirsten met music therapist, Becca. Kirsten said: “When one of the nurses asked if we might like some music therapy, I was really keen. At this point with my other children we would have started going to local mother and baby sessions and it was something I was really missing this time around. Olive was asleep on me during her first music session but as soon as she heard the music her little body started to react. Her eyes started to twitch and she was wriggling her little arms and legs. It was a really special moment because I’ll always remember the first time Olive heard music for the first time. It’s a memory I can keep when so many other moments were taken away.

“Music is obviously really emotive and I find the music sessions very emotional. Perhaps it’s an opportunity for me to let my feelings out a bit too. It’s something you can immerse yourself in that helps you escape from the clinical environment of the ward into a bit of normality for a while. Becca is so lovely and gentle – the exact bit of calm you need in amongst all the chaos. She’s the exact person you need about when everything else is such a whirlwind.

“It’s impossible to imagine what the NICU experience is like until you’ve experienced it. I know because up until now, I had no idea either. To have a bit of normality and that opportunity just to connect with your baby, genuinely does makes the world of difference.”

04/08/2026

Last year, Lewis from Aberaeron, spent seven long months as an inpatient at the Noah’s Ark Children’s Hospital for Wales after being diagnosed with Guillain-Barré syndrome, a rare neurological condition that caused him to lose the ability to walk. He missed Christmas at home, underwent intensive treatment and physiotherapy, and slowly began rebuilding strength and confidence with the support of hospital staff.

Today, Lewis home, back in school, and enjoying his childhood – all simple things that felt frighteningly uncertain for a while.

This year however, Lewis was one of the real life superheroes at our Superhero 5k. Lewis’ mum, Liz, said: “Last year we didn’t attend because Lewis wasn’t able to walk, and it just didn’t feel right for us as a family. This year though, we joined as part of Freddie’s team.

“We had no idea how much of the 5K Lewis would be able to do. He absolutely smashed it, walking and running the first 2K. It was such an emotional moment for all of us. This time last year he’d only just learnt to stand again, so to see him sprint over that finish line was something we could only dream of not so long ago. We are beyond proud of him.”

Lewis’ story is what the Superhero 5K Fun Day is all about - celebrating the determination and tenacity of children and young people cared for at the Noah’s Ark Children’s Hospital for Wales.

Share the love with a warm cup of tea ☕️By hosting your own fundraising tea event this summer, you could help fund a hot...
02/08/2026

Share the love with a warm cup of tea ☕️

By hosting your own fundraising tea event this summer, you could help fund a hot drink for a worried parent, a listening ear on a difficult day, or even a life saving piece of equipment for a child who needs it.

Your free fundraising pack contains everything you’ll need to organise a tea-rrific event, from recipes, ‘how to’ tips, invites and your very own Noah’s Ark cake toppers.

Register for your free tea party pack here: http://bit.ly/4jdwHWg

Address

Noah’s Ark Children’s Hospital Charity, Upper Ground Floor, Noah's Ark Children's Hospital, Heath Park,
Cardiff
CF14 4XW

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

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