Boy, three, nearly died from common child viruses

Three-year-old Freddie lying in a hospital bed with a tube going into his mouth attached with skin coloured tape. His eyes are closed and a teddy is visible in the background
Three-year-old Freddie needed emergency heart surgery at Bristol Children's Hospital in June [Vickie Julian]

A three-year-old boy was left fighting for his life after a rare combination of common childhood illnesses meant his heart started shutting down.

Vickie Julian, 37, from Brecon, Powys, took her son to the GP on 16 June thinking it was a cold, but days later Freddie was rushed to Bristol Royal Hospital for Children for emergency heart surgery.

He was deteriorating quickly and the final option was a life-support machine which would re-oxygenate his blood and give his little heart a rest.

It worked, making Freddie the first patient in the UK to be saved by the new Extracorporeal Membrane Oxygenation (ECMO) machine, according to the hospital.

Vickie noticed her son had a cold on 15 June and took him to the GP, who told her it was a virus.

Within days he stopped eating then "his arms were freezing cold, his lips were blue and his eyes were in the back of his head," she said.

Vickie and her husband Steven, 45, took their son to Prince Charles Hospital in Merthyr Tydfil where a cardiac paediatrician scanned his heart.

"He said his liver was about four times the size it should have been, his heart was swollen and there was fluid around it - it just wasn't beating," said Vickie.

Three-year-old Freddie smiling at the camera, he has big brown eyes and sandy blonde hair
Vickie said: "We are so proud of Freddie - his fight and determination is contagious, just like his smile" [Vickie Julian]

Doctors found Freddie had slapped cheek syndrome, pneumonia, enterovirus and rhinovirus - which often cause the common cold.

"Slapped cheek was the dominant virus in his blood and Freddie didn't even have red cheeks, but somehow this virus got into his body and it managed to attack his heart," said Vickie.

He was rushed to hospital in Bristol on 20 June where a temporary pacing wire was put into his heart to prevent it from stopping.

"They threw everything they could at Freddie for five days, he was on about 15 different life support infusions.

"He was he was so puffy because his kidneys weren't working, he was just filling full of fluid."

Extracorporeal Membrane Oxygenation machine, a tall machine with wires coming out of it. Behind it is Freddie in a hospital bed with a coloured blanket covering him
The Extracorporeal Membrane Oxygenation machine works by removing blood from the patient and re-oxygenising it before pumping it back into the body [Vickie Julian]

Doctors put Freddie on a kidney filter, but he deteriorated throughout the day.

"He was so scared," his mum said.

Finally, the only option was to put him on the new ECMO machine - similar to the heart-lung bypass machine used for open heart surgery, according to Great Ormond Street Hospital.

The machine delivers oxygen to the blood by working as an artificial lung membrane, continuously pumping this blood into and around the body.

Bristol Royal Hospital for Children said the new ECMO machine was more portable than the version it replaced and allowed the team to monitor patients while they are attached to it.

Vickie said surgeons explained it was a "last chance life support" that was Freddie's only hope.

She said that was "the scariest thing to hear".

After five-and-a-half days, Freddie's heart was rested and doctors had cleared his other infections.

Vickie said her son was "so unlucky to fall so poorly with the viruses attacking his heart" and that, if it was not for the ECMO machine, "he definitely wouldn't be here".

The machine that saved her son is being named after him, she added.

"He's a determined little boy. Everyone I speak to is just like, 'he's just a force of nature'," she added.

Vickie Julian and dad Steven Julian pose next to Freddie who is lying in a hospital bed. He has multiple wires attached to him and is covered with a brightly coloured blanket, in his arms is a soft toy
Mum Vickie and dad Steven have taken it in turns since June to sleep next to Freddie in hospital at night [Vickie Julian]

Four weeks later, Freddie was transferred to a hospital in Cardiff where he began intensive neurological rehabilitation for speech, language, physio and play therapy to "try and get him back to the little boy he was before," said his mum.

"When he came here, he had no head control, he was like a newborn baby, he couldn't move his arms.

"Now he's sitting up, he's in a walker putting one foot in front of the other - and he's paying attention to choosing toys and babbling."

Freddie grinning at the camera, he is wearing a Spider-man cap and is strapped into his wheelchair. He is outside, grass is visible in the background. A tube and tape is on his cheek
Freddie is lucky to have survived, says his mum [Vickie Julian]

For a long time he refused to eat and did not like anything near his face "because of everything that he's been through".

But after weeks of rehab, Freddie began eating and drinking and loves Skips and Giant Wotsits in particular.

"They're doing everything they can here at Noah's Ark to bring him on as much as they can, with a view to us hopefully going home before Christmas. Which would be the best Christmas present, us all back together."

Freddie is strapped into a wheelchair with tape and a tube going into his nose. He has sandy blond hair and big brown eyes and is grinning with his hands in the air. He is wearing a white Noah's Ark shirt which matches his sister Millie who is stood next to him with streamers in her hands. She is five years old, has brown hair a big brown eyes - she too is grinning at the camera
Freddie and sister Millie have been able to see each other regularly despite being so far away because of housing provided by the Ronald McDonald charity [Vickie Julian]

Vickie said she wanted her family's experience to show other parents that "if something doesn't feel right, then it's really not - don't hesitate to take your children to be seen".

"Never in a million years did I think Freddie was on death's door.

"We're just lucky there's the pioneering technology which he had access to,and the right decisions being made at the right times which saved his life - and we're so grateful, we owe them everything."