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Home » ‘My child was locked in his body until simple gift opened up his world’
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‘My child was locked in his body until simple gift opened up his world’

thebusinesstimes.co.ukBy thebusinesstimes.co.uk30 November 20253 Views
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‘My child was locked in his body until simple gift opened up his world’
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As we the Mirror launch our Christmas campaign, we meet 13-year-old Felix, who has a life-limiting condition, and who uses assistive tech from Lifelites to communicate with his family. Back in January, he met the Princes of Wales, at Tŷ Hafan Children’s Hospice in South Wales

20:28, 30 Nov 2025Updated 20:43, 30 Nov 2025

When 13-year-old Felix Forbes met the Princess of Wales back in January, his courage and determination stole her heart. Catherine was visiting Tŷ Hafan Children’s Hospice in South Wales, where she was announced as the new Royal patron, following in Princess Diana’s footsteps. It was a dream come true for the Forbes family – mum Alex, 44, dad Dan, 43, and Felix, 13, Lottie, 10, and Maggie, five. Just a few months earlier Felix, who has rare neurological condition Miller-Dieker Syndrome, had been so unwell his family feared he would die.

Of the 100,000 children in the UK and Ireland with a life-limiting condition, Felix is one of 15,000 that benefit from Lifelites, tech that helps him connect with his family, learn and have fun. Lifelites provide seriously ill and disabled children the chance to play, create and communicate, using the power of assistive and sensory technology. The charity makes the impossible possible for children with the most complex conditions.

And today the Mirror launches its Christmas appeal in aid of Lifelites to ‘Unwrap the Magic of Christmas’ for thousands of children to raise vital funds for them to experience the wonder of this life-changing technology, which includes the Eyegaze, Soundbeam, Magic Carpet, Sensory POD, Cosmo and Switches. Indeed, without Lifelites, Felix would have stayed “locked in his body”. His family would have no idea just how cognitively able he is. It’s opened up the world to him and given them the joy of connecting as a family.

There are still 85,000 children without access to Lifelites. And Mirror readers can help thousands more receive this life-changing gift, to enhance the life of a seriously ill or disabled child and help them make the most of the precious moments they have with their families. CEO Rob Lightfoot, says: “There are thousands of seriously ill children out there that we cannot yet reach. Their worlds are shaped by medical complexity, constant uncertainty and profound isolation.

“For families living with this uncertainty, there is no time to waste – every moment is precious. The complexity of a child’s condition can put simple joys – playing, laughing, learning and connecting painfully out of reach, Lifelites exists to give those moments back. Moments that may seem small, mean everything – a child painting art for the fridge using only their eyes, siblings playing a game together for the first time, a child expressing themselves through music or a family hearing ‘I love you’ for the first time.”

In a moving appeal video, featuring children whose lives have been changed by access to Lifelites technology, it’s asked, “What does Christmas Mean To You?” It begins: “Christmas is a time of magic and wonder, a time for writing letters to Santa, enjoying the warm glow of Christmas lights, having fun in the snow, visiting fairytale worlds where dreams come alive and being close to the people who love us the most.” For children with life-limiting conditions these special moments are often out of reach. Not anymore. And Felix is a wonderful example.

Mum Alex has shared her story with the Mirror to help readers understand how vital the technology is and how it has the power to unlock a child’s world. “When pregnant with Felix I had a condition called polyhydramnios, which is too much amniotic fluid. A scan at 37 weeks found that the left ventricle in his brain was slightly bigger than it should be. When he was born, scans found two cysts on the back of his brain, though he was doing everything a newborn should otherwise. Then, two months later a further scan revealed the surface of his brain looked abnormal. An MRI confirmed he had Miller-Dieker Syndrome.

“When we had the diagnosis it was as if he had died, it was horrendous, especially as we were told that children with Felix’s condition didn’t live past infancy. We had to deal with that and the knowledge that he would be fully dependent on us, wouldn’t be able to walk and talk, he’d have seizures daily, wouldn’t be able to eat orally, he’d have to be peg fed. It was a massive shock.

“It was a really lonely time. Nobody could understand what we were going through. When we were introduced to Tŷ Hafan Children’s Hospice when Felix was nine months-old we were reluctant to go as we thought it was a place children go to die But once there it was the complete opposite – a celebration of life. They took us under their wing and said let’s celebrate Felix every day. We no longer felt alone.

“Felix was first introduced to Lifelites technology at seven, using the Eyegaze and Soundbeam to play music which brought him joy and connection. But until he was 10 we had no idea he had any cognitive ability to make decisions. Then, one day he was using the Eyegaze playing a cause-and-effect game, and he posted a letter in a letter box. It was mind blowing. All of a sudden we realised he did have cognitive ability. His action was so intentional.

“I thought, ‘If he understands this then what else can he do?’ It’s opened up our world. He even won a Mario Kart competition at school using adaptive controllers. This time last year Felix was rushed to the high dependency unit at the University Hospital of Wales in Cardiff after a cold led to complications. As his condition worsened doctors broke the news that he wouldn’t make it through the night, so we decided to take him to Tŷ Hafan to pass away peacefully.

“As we arrived, everyone was in a sombre mood, the staff who had known Felix most of his life, were in shock. But as soon as he arrived he relaxed. His actions told us he felt safe. We stayed up with him all night, he saw what we thought would be his last sunrise… but it wasn’t. Felix fought back and instead of saying goodbye we started to plan to bring him home in time for Christmas.

“Our son has enriched our lives so much. Everything is so much brighter with him here. When we were asked the day before the Royal visit if we would like to meet Catherine we were so excited. It was surreal. We are the same age and both have three children. She was very warm and the chat was like a mum to mum. She asked what it’s like when Felix is in Tŷ Hafan having respite care and she said: ‘You can do more things with the girls’ and she spoke about how she saw the bigger picture. It was lovely talking to her.

“She asked about the painted hand prints on the wall and we told her that all of us apart from Maggie had done them. She turned to Maggie and said: ‘I’m going to do mine later, do you want to do it together? When Catherine went to do her hand prints we were called in and she painted Maggie’s hand. Lottie wanted to get involved too and Catherine picked up on that, saying to Lottie: ‘Do you want to paint my hand?’ Lottie said yes straightaway. It was a day we’ll never forget. Felix really is our miracle boy, he has defied the odds and now he’s a teenager and into his music and games, it’s amazing.

Felix is able to play music on the Eye Gaze with his dad, using his eyes to make the notes while Dan plays along on his own guitar. It gives them both joy. His favourite song is Hero by Foo Fighters. Lottie is also learning to play an instrument and when Felix is playing the Eye Gaze it feels like normal family time. Every day is precious and Lifelites helps Felix connect. The Eye Gaze has given us another level of understanding with him and I know he’s having fun. That’s priceless for us.

When we found out Felix had cognitive ability it opened up a whole new world that we never thought we’d be part of so it makes me sad that other families will never know what their child is capable of if they can’t access the technology, It should be made accessible to more children – it’s vital as it will change everything for those families and those children.”

Unwrap the magic of Christmas

Donate today and unwrap the Magic of Christmas for seriously ill children. Donations from Mirror readers will be used to provide seriously ill children access to life-changing technology that will enable them to play, communicate and have fun in ways that would otherwise be impossible.

  • Donate online HERE
  • Text MIRROR to 70085 to give £10. To donate without receiving further updates, text MIRRORNOINFO. Texts will cost the donation amount plus one standard network rate message, and you’ll be opting into hearing more from Lifelites.
  • Donate by post: Send cheques made payable to Lifelites to Lifelites, 60 Great Queen Street, London WC2B 5AZ

Delighted to make a difference

Rob Lightfoot, CEO of Lifelites, says:

“I will never forget the first time I visited a children’s hospice. It is a daunting experience. But Felix and his mum Alex showed me what it’s all about – life. Alex wants her son to experience a childhood, filled with moments of connection and fun. And Felix wants the same. Across the UK, around 100,000 children live with life-limiting conditions. Their lives are shaped by medical complexity and uncertainty – and often short. But in the midst of all this, their families want what we all want – to give their children a childhood.

At Lifelites, we bring the power of technology to 15,000 seriously ill children a year. With special equipment – like eye-controlled computers, virtual reality, interactive sensory worlds and accessible gaming – children can play, create, and connect with the people they love. This technology helps children, like Felix – who may not be able to move or speak – to express themselves, their hopes, their ideas, and their smiles – often for the very first time.

I’ve seen children paint pictures using only their eyes. I’ve seen brothers and sisters laugh together, play together as equals. I’ve seen parents receive their first ever Christmas card, created independently by their child using Lifelites technology. Lifelites is the only charity in the UK carrying out this vital work – if we don’t do this, no-one will. And there are thousands more seriously ill children we have not yet reached.

Every child should be able to experience a happy childhood and the magic of Christmas. To do this, we need your support. So we ask Mirror readers to open their hearts. With your donation, you can bring magic and wonder to a child who needs it most. Please help Lifelites unwrap the magic of Christmas.”

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