Colin is Grandad to heart warrior Ezmé-Rae who had open heart surgery at the Leeds Congenital Heart Unit (LCHU) three years ago.
Colin wanted to give back in thanks for the amazing support his son and family received whilst in hospital so chose to do something big and climb a mountain to raise money for Children’s Heart Surgery Fund!
Colin says that because of the wonderful Mr Giuseppe Pelella and team at LCHU, he gets his Saturday morning breakfasts with his beautiful granddaughter.
Colin said:
“We took on Mount Toubkal which is the tallest peak in North Africa. But this was about so much more than just reaching the summit. From the early start in Marrakech and the gruelling push to base camp, to setting off at 3:00am in the pitch black to catch the sunrise at the top. You definitely question your sanity on these mountains, but moments like that make it all worth it.
“The biggest victory though is why we did this. We took on this challenge for Children’s Heart Surgery Fund and thanks to the unbelievable generosity from everyone back in my local village of Conisbrough and beyond, together we’ve raised an incredible £7,230!️
“A special thank you to Conner Kelsall who supported me with social media and spreading awareness of the challenge, and a massive thank you to every single person who donated and supported the cause. And to Marc, Derick, Kev Roberts, and James Lodge – I wouldn’t want to climb mountains with anyone else. We did it!”
Once they were back in the UK, Colin and his trekking team held a celebration event for friends and family to announce the incredible total raised for CHSF! The event was held in The White Lady in Conisbrough, where Colin enjoys his breakfasts with Ezme-Mae.
Community & Events Fundraiser Lauren went along to the event say a big thank you for all their amazing fundraising.
Lauren said:
“It’s been a pleasure to get to know Colin and see his determination get him through to complete this challenge! He has an amazing support-system around him with family, friends and locals who were fantastic in helping him smash his original fundraising target. It was a pleasure to attend his celebration evening and present him with his cheque.”
Feeling inspired?
Whether you climb a mountain…or do something a bit less energetic we’d love you to fundraise for CHSF!
Leah and Brad found out the 20 week scan that their daughter, Mabel, had Coarctation of the aorta, a large Ventricular septal defect (VSD) and a smaller left side of the heart. She had open heart surgery at five days old.
Now Mabel’s family are taking on the Leeds Inflatable 5k to raise funds for CHSF, to say thank you for the care they received.
“Mabel was born in December 2025, but our heart journey began much earlier. At our 20-week scan, we were told that Mabel had serious heart problems. Like the 13 babies in the UK who are diagnosed with congenital heart disease (CHD) every day, Mabel would face challenges from the very beginning of her life.
“From that moment on, we were cared for by the amazing team in Leeds, and throughout our journey there were many charities that supported us. However, the charity that made the biggest difference to our family was Children’s Heart Surgery Fund.
“When Mabel needed open heart surgery, they gave us a place to stay near the hospital, providing us with so much more than just accommodation. We had our own private bedroom, bathroom, kitchen, dining area, living space and laundry facilities – a safe and comfortable place to stay close to our little girl while being so far from home.
“They also helped ease the financial pressures of our stay by providing money for washing facilities, toiletries, food and other essentials. Their kindness didn’t stop there. Mabel received a Katie Bear, a medal and a certificate to celebrate her incredible bravery after open heart surgery. Her big sister, Delilah, was also made to feel special with a Super Sister sibling certificate.
“Throughout our stay, Katie Bear paid visits with gifts, and the charity made sure Christmas was magical despite everything we were facing. On Christmas Eve, they brought presents for us and both girls, and on Christmas morning we woke up to huge bags of gifts waiting outside our door. During one of the hardest times of our lives, CHSF brought comfort, joy and hope when we needed it most.
“What many people don’t realise is that Children’s Heart Surgery Fund does so much more. They provide things like home heart-monitoring devices, training for cardiac staff – the list goes on. They are not a government-supported charity, so everything they do is only possible thanks to donations and fundraising.
“Quite simply, we couldn’t have made it through our journey without them.
“This is why on 20th June, me, Brad, Alicia and Kenisha will be taking on a 5K Inflatable Run to raise money for the incredible Children’s Heart Surgery Fund.
“We want to give something back to the charity that gave so much to us and helped carry our family through the toughest chapter of our lives. Every donation will help CHSF continue supporting children with heart conditions and their families, providing practical help, comfort and care when it is needed most.
“Thank you for supporting us, supporting Mabel, and helping other families facing a similar journey. Every mile we run is for Mabel, and for every child and family who needs the support of Children’s Heart Surgery Fund.”
A huge thank you to Leah, Brad, Alicia and Kenisha who are taking on the 5K Inflatable Run to raise funds for CHSF tomorrow! Please sponsor them if you can! www.justgiving.com/page/leah-rattenbury-1
A donation today helps us continue providing practical, family‑focused support to babies like Mabel and their loved ones throughout treatment and recovery.
Please help us continue to support more families who need us.
Heart mum Danielle shares her experience of daughter Matilda’s heart condition – from diagnosis at 20 weeks to the time they spent at Leeds General Infirmary and once home.
She’s now taking on a 100km Ultra Challenge to give something back to CHSF after the support her family received along the way.
“When I was around 20 weeks pregnant, I had an amniocentesis due to a suspected chromosome normality. It was during that scan that the consultants noticed a problem with Matilda’s heart.
“I was sent straight for a scan with the cardiology team and they initially diagnosed Hypoplastic left heart syndrome (HLHS). They said that Matilda would need several operations and may not live beyond five years old – which obviously broke us.
“But as her parents we had to keep fighting for her. I had scans every week – sometimes several times a week – and towards the end of my pregnancy, a scan revealed that it her heart issue wasn’t HLHS afterall and was Coarctation of the aorta (CoA) and Bicuspid Aortic Valve (BAV).
“I had a planned induction at Leeds General Infirmary (LGI) and we stayed there for around one month. Matilda had open heart surgery at five days old and had a keyhole surgery at five months old. She now has scans around every nine months and is doing amazingly well!
“During one of the most difficult and emotional times in our lives, CHSF were there in so many ways. Whilst in hospital we felt totally helpless, but Children’s Heart Surgery Fund were there to offer emotional support, and also financial support too. We lived in Eckersley House whilst there which we are extremely grateful for (CHSF make a donation towards this accommodation each year). CHSF provided us with a grant so that during the hardest time of our lives, at least the financial strain was reduced.
“They helped to provide food vouchers while staying in hospital, small but meaningful gifts like Katie Bear (their mascot teddy), certificates and medals for heart warriors, and crucial emotional and psychological support for families going through similar experiences.
“The Charity still support me now. I am in regular contact with the team and I am so grateful that I am able to turn to CHSF for support. Their social media page has also enabled me to reach out to other heart warrior mums which has helped so much. Thank you so much for all you have done for me and my family!
“On Saturday 4th July to raise funds for CHSF, I am taking on the Peak District 100km Ultra Challenge. I want to give as much back as I can and raise as much awareness as possible. In many ways, I keep thinking… ‘if I can get through those moments and the pain of seeing her go through that, then I can get through this challenge too.’ This run is my way of turning that experience into something positive.
“I’ve wanted for a long time to give something back but never felt able to do anything meaningful enough. I may not be able to change what we went through, but I can take on something that pushes me to my limits to help support other families who will go through the same thing.”
Danielle is taking on the Peak District 100km Ultra Challenge to raise money for CHSF and to support other families going through similar experiences. If you’d like to support her, you can donate at www.justgiving.com/page/danielle-nugent-5
Matilda turned 2 on 24 May, because of you!
We want to shout the biggest “Happy Birthday” to Matilda from all of us at Children’s Heart Surgery Fund.
We hope you have the best day!
A donation today helps us continue providing practical, family‑focused support to babies like Matilda and their loved ones throughout treatment and recovery.
Please help us continue to support more families who need us.
After Nelly’s Tetralogy of Fallot repair in September 2024 her parents wanted to give back, so took on the ‘Have a Grand 2025’ fundraising challenge with the aim of raising £1,000.
They opened their JustGiving page in January 2025 and by the end of the year raised an incredible £12,468 for CHSF!
We spoke to the family to find out how they raised so much money and to help give inspiration for future fundraising challenges…
Hi Philippa and Harry, thank you so much for the amazing fundraising you’ve done this year. Your fundraising will make such a difference and we’re so grateful. What made you want to partake in this 2025 challenge?
“Before Nelly was born we had no idea she had any medication complications, in her first year she spent a lot of time admitted into hospital for various surgeries and medical needs. There are so many teams we could have supported and wanted to give back to, but without her heart surgery, there’s a good chance we wouldn’t still have Nelly with us now.
“We were told without the surgery she wouldn’t make it to the age of two, and even with the surgery she had a 20% chance of not pulling through. Although it was such a difficult time, we are one of the lucky families and wanted to make sure we could do all we could to ensure future families in similar situations had the same support we did during our hardest times.”
Nelly had life-saving open heart surgery at just 7 months old at the Leeds Congenital Heart Unit. Nelly is celebrated her first heart day in September.
Read her full story here.
Why did you want to do the ‘Have a Grand 2025’ challenge as opposed to any other challenge?
“We felt ‘Have a Grand 2025’ gave us the flexibility to do a number of fundraising initiatives throughout the year whilst we both worked full time, raised two young children and to raise as much as we could financially for the charity.”
What fundraising activities did you do to raise as much money as you did?
“We started off by setting up our JustGiving page and sharing it on our social media. We have a big family but were still completely blown away by the initial influx of donations made by family and friends.
“We wanted to plan something for later in the year where people had the chance to get something back for their donations so decided we would host a family fun day fundraising event with a raffle, live music, catering, soft play and bouncy castle.
“We reached out to local businesses to ask for raffle prizes and were incredibly lucky with the prizes we were donated. We ended up with over 70 prizes with a combined prize amount of just short of £4,000 from overnight stays, to restaurant vouchers, hair and beauty treatments, family tickets, hampers and gift sets. We sold raffle tickets 5 for £10 and raised over £5,000 in selling raffle tickets alone.
“We got a discounted rate on the venue, soft play and bouncy castle due to the event being for charity and had family and friends who are in the music industry to provide live music. Although we saved a lot of money by doing it this way, we put a lot of our own time, effort and money into creating the fundraising event, but it was so worth it for the amount of extra donations we raised.
“We also held a further awareness and fundraising event at a local rugby club, and held a bake sale at a large local businesses head office.
“We wouldn’t say it has been easy – and at times has been like having another full time job outside of work and raising the children – but all the hard work we put in really has paid off. We’ve raised so much more than we ever imagined when we first decided to take on the challenge.”
Is there anything you’d say to future families taking on fundraising challenges?
“It really is what you make it, but equally we have been so incredibly fortunate for all the adhoc donations made by family and friends. We really couldn’t have achieved half of what we have without them and are beyond grateful to everyone who’s contributed towards the final amount raised.
“Whether it was family and friends, local businesses, our own employers, people we don’t even know who contributed, we appreciate every single donation and are so happy we’ve been able to give something back to the charity that supported us so much throughout Nelly’s heart surgery.
“Anything at all goes towards making such a difference to families going through some of the toughest times and we’ll forever be grateful for what the charity helped us through.”
We can only keep being there for our life-saving heart unit, patients and families with your help. Make a donation today to help us continue our vital work.
What? The Big Give #ChristmasChallenge is our Christmas campaign for this year and all donations you give NOW are doubled – but please hurry, the campaign doesn’t last long!
When? Tuesday 2nd December midday – Tuesday 9th December midday
Why? To fund parent accommodation for our families. Give NOW and double the impact for your donations, reducing worry for future mums and dads of children being treated at the Leeds Congenital Heart Unit.
This is why parent accommodation is so important…
Heart hero Alex was born with a right sided aortic arch and a small Ventricular Septal Defect. His dad Ollie told us:
When the team told us a room was available for us to use, we were so relieved and grateful to be able to stay close by – it allowed us some personal space, but we were close enough to be on hand quickly.
Heart hero Victor Bear, from Keighley, had three open heart surgeries in his first year. His dad Luke told us:We knew we needed to rest ourselves, but the guilt of leaving Alex’s bedside was significantly reduced knowing we could get back to it in minutes.
The parent accommodation was a godsend, as it meant even when we were tired, we were only a short walk away. It was like a mini home-from-home when our world was turned upside down.
It meant we could take turns to sleep, and give us chance to wash our clothes and eat proper food rather then the cost of eating in the cafes or takeaways.
Last year we provided 2,555 nights of parent accommodation to 300 families in CHSF’s rooms on Brotherton Wing and at Eckersley House giving families vital respite, and saving countless hours of extra travel, cost and worry.
With your help, we can continue to do this!
FAQs about The Big Give with CHSF The Big Give is a UK-based charity that runs match funding campaigns, which allows donations to charities to be doubled by connecting them with funders. Through its online platform, it helps thousands of charities raise funds for a wide range of causes by securing match funding from philanthropists, foundations, and the public.The Big Give works by matching public donations with funds from pledgers and “Champions” (philanthropists, foundations, or companies) to double the value of each donation during specific fundraising campaigns. Our pledgers are Womble Bond Dickinson, Morley Glass, J9 Advisory and Irwin Mitchell and our charity champions are Reed Foundation. Together, they will match fund any donations YOU make up to £6,500 – meaning your fundraising will be doubled. Simply donate
here, and any donations made up to £6,500 between midday Tuesday 2nd December and midday 9th December will be doubled by our charity champions.Donations made to this campaign will go to parent accommodation funded by CHSF – both in our rooms at Brotherton Wing and through Eckersley House, run by the Sick Children’s Trust. We have supported Eckersley House for over 15 years with regular donations. You certainly can! But please just donate through our usual channels, as the donation will not be doubled after that time.
A huge thank you to our pledgers this year, who have made up our matched giving pot! Take a bow – Womble Bond Dickinson, Morley Glass, J9 Advisory and Irwin Mitchell and our charity champion Reed Foundation!Sign up to Paint & Sip
By signing up to this event you agree to CHSF’s
Event Terms & Conditions.
Jess and Callum, parents to heart warrior Louie, organised a Family Fun Day in August this year August.
To raise even more funds for CHSF, friends decided to also incorporate a sponsored bike ride too!
Jess told us a bit more about Louie’s story and how it inspired their family to fundraise for CHSF…
“On 22nd November 2024, our beautiful boy Louie was born. We had no idea what lay ahead.
“Just two days later, we noticed Louie breathing rapidly. Instinct kicked in – we called his Nannie, who didn’t hesitate. We rushed him to A&E. The first doctor reassured us he was fine, but thankfully a second doctor immediately realised the severity and rushed Louie into resus.
“He was treated for suspected sepsis, but things didn’t add up. Later that night, our world changed when doctors told us there was something wrong with Louie’s heart. Around 4am, we were blue-lighted to Leeds Children’s Hospital by the incredible Embrace transport team. It was terrifying.
“At Leeds, we learned Louie had Total Anomalous Pulmonary Venous Drainage (TAPVD) – a rare congenital heart defect where the veins carrying oxygen-rich blood from the lungs don’t connect properly to the heart. It causes dangerously low oxygen levels and can quickly lead to heart failure if untreated.
“At just 4 days old, Louie needed open heart surgery. He was placed on a ventilator in Paediatric Intensive Care Unit (PICU), where he stayed for weeks. One night, we received the call every parent dreads – our little boy had to be resuscitated.
“Eventually, Louie was moved to High Dependency on the children’s heart ward (L51), though complications meant he was often back in PICU. He also needed further surgery to have his diaphragm sewn down.
“That first Christmas was spent on Ward L51. Nannie brought homemade Christmas dinner and treats – we tried to make it special despite everything.
“We were discharged on 27th December, but within just 30 minutes of being home in Scunthorpe, Louie declined again. We rushed back to our local hospital and were admitted to HDU. Just days later, the Embrace team returned us to Leeds.
“Louie seemed to be improving, until tests revealed he needed another life-saving surgery – to remove part of his left lung and repair his heart again. There was no ‘plan B’. Within an hour of hearing the news, he was in theatre. Our family rushed from across the country to be by our side.
“Thirteen hours later, the call came: Louie had survived. He was critical but alive.
Step by step, Louie fought through – ventilator off, drains out, pacing wires removed, chest finally closed. He moved from PICU back to L51, and later to the respiratory ward. With only a quarter of his left lung remaining, he needed extra time and oxygen support.
“On 17th March, after nearly five months in hospital, we finally brought Louie home – for real this time. He came home with oxygen and an NG feeding tube, but he was home.
“Since then, Louie has continued to amaze us. His oxygen levels are improving, and we’re hopeful the feeding tube won’t be needed for much longer. He’s started weaning and loves his food – each step is a little miracle.
“This journey has tested us more than we could ever imagine – but through it all, Louie has been our light. A warrior. A miracle.
“We are endlessly thankful to everyone at Leeds Children’s Hospital, Children’s Heart Surgery Fund (CHSF) and every doctor, nurse, porter, cleaner and support staff who carried us through.”
Lauren Procter, CHSF Community Fundraiser said:
“Jess’ family and friends really got behind their fundraising goals and it certainly shows. We are so thankful for this amazing amount raised – £8,405 currently on their JustGiving page! If any other heart families would like to know more about organising your own fundraiser, get in touch with the team as we’re on-hand to help and support!”
Feeling inspired?
Have you got a fundraising idea or want to chat through how you can help CHSF? Drop us an email at info@chsf.org.uk!
In memory of their beautiful daughter Roxy, who passed away in hospital aged just six months old, the Jackson family took on a powerful challenge – a nighttime hike up Mount Snowdon!
Surrounded by loved ones, they climbed through the darkness to raise money for four incredible charities who supported them throughout their journey – including CHSF!
Roxy’s mum Chalotte said:
“We sadly lost our amazing, small but mighty, strong, determined, feisty, chubby-cheeked superstar Roxy on February 10th.
“Roxy was born with a heart condition called Atrioventricular Septal Defect (AVSD). After two months in hospital and three major operations she sadly passed away at just 6 months old, leaving behind her twin brother Kyan and older brother Coby.
“In her memory we wanted to raise as much as possible for the amazing charities that helped to support us in the last few months.
“We chose to raise money for Children’s Heart Surgery Fund because the support they gave us while we were in hospital was amazing. They helped us financially and were just so friendly and attentive. We wanted to continue to support this charity to help other families going through a very difficult time.
“We decided we wanted to do something special in Roxy’s memory and so we chose to walk up Mount Snowdon at night – the highest mountain in Wales. As Roxy’s name means ‘star’ and she’s half Welsh, it seemed absolutely perfect!
“There were seven of us in total who did the walk. Myself and Dave, Roxy’s dad; her grandad, Howard; two Aunties Bec and Rach; her uncle Gaz and her cousin Ruby, who was just 11 at the time.
“Roxy’s brothers, cousins and Grandma helped behind the scenes – packing snacks and decorating our bags ready for the walk!
“CHSF were such a big part of our lives for the two months we spent in hospital. They think about everything and it’s vital. We will continue supporting this charity while remembering our precious heart warrior, Roxy Elizabeth Jones.”
Lauren Procter, CHSF Community Fundraiser said:
“When I heard about Roxy’s family taking on the starlight hike up Mount Snowdon, I was in awe of their determination. Mum Charlotte was telling me all about it, and how a lot of the walk would take part in the dark!
“We are so thankful that they chose CHSF as one of their charities to support with their fundraising, and we were so happy to see they raised an amazing £1,500 for our heart unit and other families in our region! Thank you!”
Feeling inspired?
Have you got a fundraising idea or want to chat through how you can help CHSF? Drop us an email at info@chsf.org.uk!
Chris took on ‘The Wall Ultramarathon’ on the 14th June 2025 – a 70-mile run along and around the historic Hadrian’s Wall.
Chris is a family friend of heart warrior Freddie McDonald. Freddie’s family are organising a fundraising ball later in the year and Chris wanted to support them by raising funds.
Chris said:
“In November last year, I signed up for “The Wall” – a 70-mile ultramarathon from Carlisle to Newcastle. At the time, it was a personal challenge (I was goaded into it by a mate!) – something extreme, something that would push me beyond my comfort zone, something that would give me focus for the first half of 2025.
“But as the training went on, the motivation behind the miles took on a much deeper meaning when I decided to raise money for Children’s Heart Surgery Fund.
“Our good mates, the McDonalds, have a strong connection to the charity through their son Freddie, who has directly benefitted from the fund’s vital work. Seeing the positive impact the charity has had on their family made the choice of who to support an easy one. I wanted to run not just for myself, but for something that mattered – something that would help children like Freddie and families like theirs.
“The training was long and often monotonous. Running through all types of weather and racking up the miles month after month can take its toll – especially when you’re juggling family and work. But having a clear purpose made it all so much more worthwhile.
“Race day itself was a rollercoaster of emotions and endurance. The day started with lashing rain, my feet were soaked within the first couple of miles, and the blisters started to appear at about mile 15.
“There were some big highs – ticking into the 27th mile, further than I’d ever run before; traversing the steep hills as I approached mile 30; meeting my wife Emma at a couple of the later checkpoints and feeling the support of fellow runners and spectators that I hadn’t met before.
“There were also tough lows where it felt like the finish might never come, particularly the last 6 miles in the dark coming into Newcastle. But knowing I had already raised over £4,000 kept me going.
“I was messaging the McDonalds from about mile 50 and remember one really funny exchange, where Freddie himself was abusing me for the colour of my (bright orange) trainers. These were the moments that kept me going!
“Crossing the finish line over the bridge into Gateshead was one of the proudest moments of my life – not just for completing the challenge, but for what it represented.
“I’m incredibly grateful to everyone who supported me and donated, and I’m proud to have done my small part to help such an important cause.”
Lauren Procter, CHSF Community Fundraiser said:
“We were over the moon when we heard about Chris’ challenge and that he was raising funds for us. What a challenge to take on – and he did so well! “£4,190 raised for our heart unit, patients and families. Thank you Chris and everyone who donated.”What an incredible challenge – and phenomenal achievement. Thank you Chris. CHSF can only do what we do because of awesome people like you!
Feeling inspired?
Have you got a fundraising idea or want to chat through how you can help CHSF? Drop us an email at info@chsf.org.uk!
After his daughter was born with CHD, heart dad Nick decided to take on the awesome challenge of walking 125 miles for the 1 in 125 born with a heart defect.
At first, he thought he’d be walking along – but in April he completed his challenge with an army of friends beside him. And they raised an incredible amount in the process…
Nick said:
“My youngest daughter Harper was born with a ventricular septal defect, that required open heart surgery at 6 months old.
“The stress for me and my partner when Harper was having surgery and also seeing her after surgery was unbearable. I cannot begin to think what it is like for the patients who are actually going through the surgery, and also other families.
“I can’t thank the Sheffield Children’s Hospital, the Leeds Congenital Heart Unit and Children’s Heart Surgery Fund enough. That’s why I decided to do this walk. 1 in 125 babies are born with a congenital heart defect, so I wanted to walk 125 miles from my home near Sheffield which roughly leads me to Watford.
“With me and my family being big Wednesday fans, we thought it would make sense to walk from our home in Mosborogh to Vicarage Road (Watford F.C’s home ground), arriving there on the Saturday when it was Watford Vs Sheffield Wednesday.
“I really enjoyed doing the walk to raise awareness and getting donations for this amazing charity! Tuesday and Wednesday’s walks weren’t great as it was just hills and walking on the A5. But my mates kept me going every day. They surprised me at the start of the walk, as I was going to do it on my own. They made sure I had a few friends with me each day. In the end, 21 lads came together to help me for this charity. I also had a few videos from Sheffield Wednesday legends to keep me going and a big donation from Sheffield Wednesday captain, Barry Bannan!
“Big thanks to all the lads who walked with me – and also Watford FC for giving me a box to watch the match with my family at the end of the finish line.”
CHSF Community Fundraiser, Lauren said:
“Nick got in touch in February to share his idea for his sponsored walk. With big dreams and his sights set, he went away and finalised everything. The Fundraising Team are on-hand to help and support with all of our fundraisers, but Nick didn’t need it! We’ve been absolutely blown away by how much he has raised. A huge thank you to Nick, and his friends for raising a phenomenal £5,872 for our heart unit, patients and families.”
Feeling inspired? Why not set yourself a challenge and raise some valuable funds for a charity close to your heart?
Register to fundraise here or email lauren.procter@chsf.org.uk for more info!
On Saturday 12th July, the CHSF team will be competing in a Dragon Boat Race – and we’d love your support!
Organised by the Rotary Club of Wakefield Chantry and Normanton, it’s a fun day for the whole family. #TeamCHSF will complete against 40 teams from local businesses, charities, and groups.
Come along to cheer us on!
As well as cheering on the teams, there will be other activities to keep you entertained including: tombola, face painting and games throughout the day. Pugneys Light Railway will be operating too, taking passengers around the park.
There will be refreshments on site with Pugney’s Café open for business along with various concessions providing a range of food and drinks to purchase. Alternatively, get the family together and bring a picnic!
Sponsor the team
As a team, we’re hoping to raise £1,000 for our world-class heart unit, our incredible heart warriors and their families.
If you can support #TeamCHSF please make a donation on our fundraising page here.
When: Saturday 12th July 2025
Where: Pugney’s Country Park [Google Maps]