Patrick’s story

Little Patrick needs your help and time is running out. The specialist care that children and families like him rely on is under threat. The care Patrick needs is in your hands.

The future for little Patrick remains uncertain. His mum Keri says she and her family take everything day-by-day – but they fear a future where the vital hospice care they receive doesn’t exist.

Every parent’s nightmare

“Life without hospice care would be impossible,” Keri says. “To imagine a world where it doesn’t exist due to lack of Government funding, and where families like mine could not access this specialist support, is unthinkable.”

Patrick, now aged two, suffered a brain injury when he was born suddenly and unexpectedly at home. In the space of a few hours, Keri and husband Andy went from excitedly expecting the arrival of a healthy baby to their lives being changed forever.

Patrick was born breech, a term used for when a baby is born bottom first instead of head first. But, being at home, Keri had no medical assistance while waiting for the emergency services to arrive.

A young boy with a tube going into his nose.
A mother and father looking down at a small baby with medical tubes going into his nose and hands.

Keri said: “It’s all a blur. I was suddenly giving birth to a breech baby with absolutely no medical intervention at all, and the thoughts of having anything wrong with the child didn’t really come into my mind.”

When the emergency services arrived, little Patrick was rushed to hospital, and it would be several hours before Keri and Andy were allowed to see him.

It’s every parent’s nightmare – they were told to prepare for the worst.

Keri said: “The following hours and days were critical and I think the hardest part was that you couldn’t hold him, with all the wires and tubes and beeps from the machines.

“You keep hearing the words brain injury, and seizure, and you keep hearing other words you don’t understand, but nothing is really explained.

Patrick’s journey to Acorns

“And then all I remember is hearing the words ‘children’s hospice’, and you instantly think the worst. I had learned, when I was young, that it was a place where children go to die.”

Over several weeks Patrick fought for survival, but Keri remembers feeling resentment when she was referred to Acorns Children’s Hospice.

“I didn’t want to come and I didn’t want to speak to anybody,” Keri said. “I certainly didn’t want to come and look around, and no matter how many people times people said it’s not like a hospital, I didn’t believe them.

“The car journey there was awkward, and we just braced ourselves. But it was like when you walk off an airplane you get hit by that wave of heat – and we walked into the hospice and just got hit with this wave of warmth and friendliness.”

A young boy lying on a patterned bed with a woman looking down at him.

“I knew from that moment that I was in the right place – and that it was a magical place.”

Acorns care and support

Keri added: “During the visit I got lost trying to find the bathroom, and I saw one of the nurses in a room with a child, and the nurse was chatting to them about the weather, and singing songs, and she didn’t even know I was there.

“I knew from that moment that I was in the right place – and that it was a magical place.”

Acorns provides rehabilitative respite to Patrick and his family, and a tailored medical plan to meet all of his needs.

He particularly enjoys therapy in the sensory room, and hydrotherapy in the hospice pool.

A father holding a smiling baby who has a tube going into this nose,
A mother holding a small boy, who has a tube going into his nose. They are both smiling at the camera.

The hospice’s specialist nursing team also supports him with pain and symptom management through hydrotherapy sessions in the hospice pool and palliative play and sensory therapy.

It was later diagnosed that Patrick had suffered Hypoxic Ischemic Encephalopathy (HIE), a brain injury caused before, during or after birth when oxygen or blood flow to the brain is reduced or stopped.

Keri is now raising her hand and urging the Government to secure the Children’s Hospice Grant and long-term funding for children’s hospice care, for families just like hers and children like Patrick. 

“What I do know for certain is that we’ll always need Acorns.” Keri added.

“The future of children’s hospice care is in the Government’s hands and it’s in the hands of the Prime Minister. It’s in the hands of everyone.” 

Children’s Care Matters

Keri is joining a nationwide call urging the Prime Minister and the Government to secure long-term funding with the Children’s Hospice Grant. The future of children’s hospice care is in your hands.

If you want to join the fight and add your voice to our campaign, visit savethegrant.com and click ‘YES’. We count every click.

Find out more