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It was simple, but it was perfect: Angie and her family’s journey

We had the privilege of talking to Angie’s children, hearing more about her, the family’s experience at the Hospice, and how fundraising supported their journey through grief and helped to make a difference in Angie’s memory.

“Mum was an unstoppable force of nature. She was strong-willed, compassionate, and completely dedicated to us – her kids. She had an incredible instinct for other people’s pain, and showed immense empathy to anybody who needed it. She lived her life for us, and she loved fiercely. Anyone who knew her felt that. We will love her endlessly, forever.”

Ange first came to Halton Haven Hospice in December 2024, and after spending time in other facilities over the next few months to support with pain management, she then returned to the Hospice in April as she wanted her end of life experience to be here.

Care personalised to her

“Mum was very nervous in healthcare environments by the time she got to be cared for by Halton Haven Hospice, but the staff gained her trust very quickly.”

“From the very first day, the staff made it clear that their priority was understanding who she was and what mattered to her. They personalised her care around her need to be surrounded by family, and they made sure she received everything she needed while still allowing us to be constantly in and out, sitting outside with her, and filling the space in the way our large family naturally does. They reassured us straight away that they could care for her to the high standard we had been trying so hard to maintain at home, with the help of District Nurses, and they proved that to us every single day.”

“There are so many moments that will stay with us forever.”

“One of the biggest was when we were able to bring Mum back to Halton Haven from another care facility where she had been trialling treatment. It was painful to all of us that the treatment had not helped, but when she returned to Halton Haven Hospice, she simply said “I’m home.”. The relief we felt in that moment is something we’ll never forget.

Another memory that means absolutely everything to us is the day that Mum’s doctor listened intently when we raised concerns about a medication that had been added to her plan at another care facility. We explained that Mum wasn’t responding in the way she normally would, and that something felt wrong. He took our lived experience seriously, trusted that we knew her best, and agreed that her reaction wasn’t typical for her. Because he believed us and acted on it, Mum woke up on what we have since dubbed “Miracle Day”, and we were able to have almost three more exceptionally precious months with her, that we may not otherwise have had.”

“They focused on Mum’s wishes, her dignity, and what she wanted her final weeks to look like.”

“The hospice made a difference in every possible way. They centred Mum’s autonomy in every decision and treated her preferences as essential. When she told the nurses or doctors that certain medications didn’t feel right, they didn’t dismiss her. They listened and tried alternatives. That level of respect meant everything. They never made her feel like she was asking too much or passed judgement on her choices. She felt understood and accepted for who she was.

They involved her and us from the moment she arrived until the very end of her time there. We never felt like we were in the way or bothering anyone. The Nurses and Healthcare Assistants even took seriously our requests to be called in the night if Mum woke up and needed comfort. They created an environment where we could simply be with her whenever we wanted to be, and that gift is something we will always be grateful for.”

Adding life to days

“In the final week of Mum’s life, we were able to spend time together as a family, out in the garden. The staff brought out trays of sandwiches and ice pops, and we spent the whole day in the sun with Mum. It was simple, but it was perfect.”

“Our Mum inspired us to fundraise”

“She was incredible at her job, and she was passionate about fighting for NHS funding. As such, she helped to found the local Momentum group around 2018, with the goal to help the NHS as much as she could. We are so proud of her, and she has inspired us to care so deeply about fundraising and helping healthcare stay available to those who need it.”

To honour the one-year anniversary of Angie’s passing, her children: Jasmine, Rayna, Laura, Ade, and their friend Shaunagh, organised an event in her memory called AngeFest. This event raised an incredible £3,465.89 for Halton Haven Hospice and “became a celebration of her, of community, and of the hospice that cared for her with so much kindness.”

For family and friends, fundraising became a way to “work through our grief in a way that felt active and meaningful.”

“Doing something for others, especially in Mum’s name, became a therapeutic way for us to process everything we’d been through. Fundraising for Halton Haven felt like the most natural way to honour her and to give back to the people who gave us so much. We want other families to receive the same level of care we did.

AngeFest was a day of live music and family‑friendly fun held at the Parklands Social Club in Widnes. We filled the space with games stalls for both kids and adults, a large luxury raffle, live music throughout the afternoon, and a really relaxed, welcoming atmosphere that felt true to Mum. It was the kind of day she would have loved: people coming together, kids running around with prizes, music playing, and everyone just enjoying themselves while supporting a cause that means so much to us.”

“Community generosity added so much heart to the day.”

Family and friends set out to create a day to bring people together and the support of the local community and businesses showed that together, we can help make a difference. “Every prize, every voucher, every service offered helped us create something joyful and meaningful in Mum’s name. It reminded us how strong our community is and how much kindness there is in the people around us. We’ll always appreciate the way they showed up for us and for Halton Haven.”

Thank you so much to Angie’s family for sharing their story. They continue to think of ways to support the Hospice, and we are grateful for the difference they are making in Angie’s Memory. “Halton Haven will always feel like part of our family now. The staff there will always be so special to us.” If you have been inspired to fundraise in memory of a loved one, please email us on fundraising@haltonhaven.co.uk so we can let you know how we can support you.

“Halton Haven is number one, there is no better place”

We had the privilege of talking with Alina, aged 32, and her twin sister, Dorina, about their experience with Halton Haven Hospice. Photos in this story were taken on Alina’s polaroid camera.

Coming to the Hospice

Alina first came to Halton Haven Hospice in October 2025 after being diagnosed with stomach cancer. Alina says “I ended up in hospital with inflammation and a high temperature. They explained I was too weak and poorly for chemotherapy and it would affect my quality of life. So, on 30th of October 2025, I arrived in Halton Haven Hospice for end of life care. They weren’t sure how long I would live, could be weeks- maximum months, because when I came here, I was really poorly.”

“She wasn’t able to eat or walk, she was losing a lot of weight.” Adds Dorina

Alina continues saying “I didn’t know what a hospice was. I didn’t know how long or what was next, I just thought I would stay here until I died. For the first couple of days, I was scared and anxious but the same evening I arrived they started to support me with different medications to manage my symptoms. After a bit I felt amazing, I could eat, I could talk and I had some energy – it has helped bring me back to life.”

But for Alina, it wasn’t just the pain management that staff at Halton Haven Hospice supported her with.

“They manage the pain which is in your soul and heart which is really important. They manage to make sure you are mentally, physically and emotionally in every way okay.”

Adding “It’s how they care, how they treat me, talk with me, support me – yeah the nurses come and ask how are you. In hospital you can feel quite alone, but here they really care. I believe and I see that this is not only their job, but they are also doing this because they love what they are doing. I love this place because people’s hearts and their desire to help people and how they care about others helps to bring patients like me back to life. You feel this energy that they are doing what they love to do, and I am very grateful for that.”

Providing the care people deserve

Alina spoke with us about the care she had received at Halton Haven Hospice saying “Halton Haven is number 1, there is no better place”

One instance she shared was “I needed to go to hospital. Scott and Donna supported me (Hospice Staff), by coming with me. It was a terrible experience for me at the hospital, but because Donna was next to me and the next morning picked me up,  that is something that I really remember. How she dealt with that situation, she really supported me. When she saw me, she hugged me, said lots of nice things to make me calm down. It was so sensitive and so nice. Donna didn’t need to do that, she could have just done her job but no, she really cared about how I felt. I really appreciate that. That is memorable because on one hand it was bad, but how Halton Haven Hospice helped me, even in that terrible situation, made me feel better.”

Hospice food that can brighten up your day

When speaking with Alina it became apparent how much food played an important part in her care at Halton Haven Hospice.

Recalling a memory Alina says “My sister was in a hotel and she sent a picture saying they had breakfast included. I saw on the picture black pudding and when the Hospice brought me English breakfast it wasn’t on there, so I was a little bit jealous. I said ‘Where is my hash brown and black pudding? I would like to try it’ and then one day one of the nurses went to the store and they cooked it for me. It was the first time I had ever tried a FULL English breakfast with black pudding, tomatoes, mushrooms, it was a huge plate. I was so excited to try everything. I had everything, like a 5-star restaurant. I took a picture and sent it to Dorina saying ‘I got the same but even better.”

“I still don’t know how I feel about black pudding though.” Alina adds while laughing.

Dorina says “It was nice because they didn’t have that on the menu.” With Alina adding “Yeah, they bought it for me specially then for three days in a row I had the breakfast.

I like the Sunday dinner as well, it is a British tradition people like to enjoy with their family, at home or in a restaurant, and when I tried Sunday roast here, I felt like this was my home. It’s something so special and delicious – I feel at home in the UK finally, I feel at home here with the nurses, it is really nice.

We also spoke previously with Alina about her room having a great view onto the front gardens at the Hospice and the bird visitors she likes to get “I save my sandwich corners to share with the birds outside my window, they need to have a breakfast as well.”

Adding life to days

Dorina shares “When I first came to visit Alina, she could barely walk and she was in bed all day, but then I came a few weeks later and she was able to walk and was full of energy. She was saying she wanted a nice evening and a party, so we went to the local pub ’Queen of Hearts’.  Alina was putting on her makeup, and we ordered pizza and cocktails, it was a very nice evening as we were outside but not too far away. We then went to the shop and bought some snacks and wine, and we stayed at the hospice till about 10pm, it was like a mini party!”

Alina joins in to share “For me I was living here alone, I didn’t have anyone to take me to restaurant or have a simple Friday night. It was the last chance to be like a normal human being, enjoy my weekend in the pub, that is what people do. I could forget about everything and just sit there and enjoy. I was so excited and anxious, but to be there and to eat pizza and enjoy nice company with my sister, that was so amazing. I feel freedom at the Hospice, people treat you like a human, not a patient so it was really nice to be able to do that.”

Dorina adds “You are allowed and free to go any time you want, if you are able. You can take a wheelchair or they said ‘just call us and we will come to you’ They are supporting you wherever you are, they are prepared.”

Talking about another moment Alina says, “People are going shopping getting Christmas gifts. I like to go to the store and sometimes I get this feeling that I want to be normal like other people. I don’t need nothing, no food or nothing, but I just want to go to the store because it’s normal. For me to pay with my card and get something, it is an exciting experience. So the Hospice lets me go shopping and do that, its small things that are nice.”

“Halton Haven Hospice care about even the small details, I feel safe, I feel like they care, this for me is wonderful and I don’t know how to share the gratitude I feel.”

Alina also played a very important role at our Light Up A Life event 2025. Read more about her involvement HERE.

Julie was safe and happy: Johns Journey

After being diagnosed with motor neuron disease (MND), Julie, John’s wife, who he describes as “a million things, beautiful, incredible, loving, fun, caring”, spent 25 days in Halton Haven Hospice for end of life care.

John says “Julie made a decision early on in her care plan that she didn’t want to die at home, she wanted to be at Halton Haven. I now have a life long connection with the Hospice as my final memories, some great memories, of Julie are there. During that time, you can imagine how close we got to the staff and everybody that worked there. It’s incredibly hard when you lose somebody you love so much however, it couldn’t have been nicer in that situation.

“The staff loved her and laughed with her, it was incredible.”

“I like this caravan”

“The doctors would come in every morning with an open ended question ‘How are you today Julie?’ and she could answer anything. Sometimes you’d hold your breath wondering ‘What will she say today’. One day she said ‘You know doctor I like it here, I’m quite happy, I like that John can stay with me and I like the fact that Rob Burrow is in the room next door.’ Obviously he wasn’t but she took huge comfort in thinking that Rob was next to her. Towards the end of her life Julie started to believe that her hospice room was actually a caravan. She would say ‘I like this caravan’. It became our joke. Our last 25 days were spent in Room 2 at Halton Haven Hospice and there are many lovely stories and great memories that we still have.”

Made to feel welcome

“We almost created a home from home, people came and went we had the freedom to do that. I stayed on a pull out bed in Room 2 for 21 nights. On a night time I would go sit in the lounge and the staff would always come over and ask me ‘how are you today?’. I wasn’t the patient, it wasn’t about me, but they would come and have their tea with me and whoever was there would ask if I needed anything. I was led through what was likely to happen as she approached end of life, so I was always involved and aware what was happening with Julie. I liked the way they accommodated me to be with Julie.”

I never got the feeling I was in the way, the staff were as beautiful with me as they were with Julie.

Preserving Memories

“Throughout her illness I kept a diary of milestones, daily occurrences, and memories. It started quite small but as Julie’s health deteriorated and she slept more, then the diary entries got bigger. At the end of every day, I would send the diary entry out to everyone in our family unit so everyone knew at 9pm they would receive their daily update. After Julie died, that’s when I really found a lot of comfort in writing, reminiscing and preserving what memory I had while it was fresh in my mind.”

John is now in the process of releasing his own book filled with these memories called “No Plan B”. You can pre-order the book here: Books – Scratching Shed Publishing

Fundraising in memory

In memory of Julie, John, family and friends have raised over an incredible £13,000 for Halton Haven Hospice. With plans to raise even more going into 2026. “I feel like I need to raise enough to make sure people in the future have the same opportunity we had. The quality of care that Julie received at the Hospice was incredible. Julie was somewhere safe and happy, that’s priceless.

John has attended many of our Hospice events and even read a poem at our Tea at Three event, but one of the main ways he has supported us is through doing walks, including a sunrise walk up Snowdon, a 14 mile walk from Spike Island to the Royal Liver building, and on the anniversary of Julies death he walks from his home to the Hospice.

“Yes, it’s about fundraising but the silver lining is doing something special as a group of people that gives you a connection. I can’t undervalue how important that is.”

Talking about another walk John says “All the teachers I used to work with joined me on a walk from Preston to St Helens (26 miles). When we set off none of us knew if we would finish. The main memory from that event is before we did the last 500 meters we all stopped so we could walk across the finishing line together. That feeling of completing such a big challenge in memory of Julie was overwhelming. When you achieve something that is so personal, it was a beautiful moment. All day we were catching up with old friends, it was a brilliant day, and I am proud we did it. When people give up their time it is really special.

Thank you so much to John and all Julies’ family and friends for raising awareness and funds for Halton Haven Hospice. Do you want to get involved? Email fundraising@haltonhaven.co.uk to find out how you can help add life to days.

A light in a very dark tunnel: Jayne and her family’s story

In 2024, Jayne’s husband Ste came into Halton Haven Hospice for end of life care, after being diagnosed with bowel cancer nine weeks previously.

Jayne shares “Ste was a family man, we went to school together in Runcorn since we were 13, everyone knew Ste and he knew everyone. He was really friendly, outgoing and obsessed with Liverpool football club. Even though he was in a wheelchair for 17 years, it actually never stopped him from doing anything. Ste grew all our fruit and veg at home on our farm, his life was doing the gardens and growing stuff for the family. Family, friends, and sport were most important to him. Then this came out of the blue.

We wanted to keep him at home, but he was far too poorly. So he bravely made the decision to come into the Hospice. We went from on our knees caring for him 24/7, to ‘Right this is our job to care for Ste now, you go back to being his wife and his family’ which was absolutely brilliant. We knew a couple of the carers at the Hospice and they looked after us and looked after Ste.”

He was treated like a king.

“When we got to the Hospice they said to us ‘have you got any pictures you want to put up?, how would you like the room to look?, do you want to bring any pillows ? – we were like rabbits in headlights – you think it’s a hospital but they asked for 10 minutes to settle Ste in. When we came back the room was decorated with pictures and everything we had brought in. It was just like ‘wow’ how did they know he wanted that, it was just amazing. It put us at ease.

We’d have Stes’ favourite music playing and we’d have a laugh, we’d do McDonalds orders, and one night friends visited and we had a party on the front garden, it’s such an open place. One of our granddaughters was only three at the time and we thought it wasn’t really fair for her to see him when he was really poorly so they said let her go round the back and she can sing to him through the window and she did. Halton Haven Hospice took the element of being carers away and enabled us to be his wife, daughters, his son just for that week.”

The Hospice truly is a light in a very dark tunnel. You never think and never hope that you need a hospice, but if there is a time that you do, this is the place you’ll want your loved one or yourself to be.

Family and friends now fundraise in memory of Ste

We will never be able to thank The Haven and Staff enough for the time we spent with them, but by raising money we would like to think we are helping this wonderful place to continue, so that another family just like ours gets some comfort during the most difficult time of their lives. We are forever grateful.

Since starting, Stes’ family and friends have been fundraising in many ways from collecting contributions at Stes’ funeral, getting involved at our events, to getting local school children involved in brightening up the Hospice. “My daughter is a teacher, so we arranged a trip to the Hospice with the whole gardening club. They planted daffodils all around the garden last October.”

Running and other physical challenges have played a big role in their fundraising. “I do a lot of runs like the Great North Run and I am also doing the Vietnam to Cambodia challenge in 2026. My two sons in law and my friends husband did the London marathon. Our friend Mark did Land’s End to John O’Groats and we have done the Christmas Elf Run too.

39 of us went to London to support everyone doing the London Marathon and we had a nice weekend. My sons in law were proud as punch that they had done the London Marathon and the money raised was amazing, but it was also really fitting as it was the weekend Liverpool won the league. Ste would have loved that weekend. One of the lads who came down to London actually got the train straight back to Liverpool to celebrate. I found that a good memory as I will tell you now, it doesn’t matter who had been running the marathon, if Liverpool was about to win the league Ste would be looking down at London but then gone straight back to Liverpool.”

Thank you so much to Jayne for sharing her story, as well as to all Stes’ family and friends for the support they have given Halton Haven Hospice in memory of Ste. You can find their JustGiving page by clicking HERE.