A boy who died after his stillborn needs £ 100,000 for a normal life



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He has fought more battles than most people in his life and is not yet two years old.

Theo Hutton returned from the dead seven minutes after his death, while his brain was lacking oxygen.

The atrocious birth has left him cerebral palsy and he is unable to sit, walk or talk.

But despite her ordeal, Theo still has a big beaming smile, and her parents, Laura and Andy, feel he is the happiest little boy there is.

Now the couple wants to improve their chances later by collecting £ 100,000 for various treatments abroad.

They include pioneering stem cell surgery – not yet available on the NHS – in Panama.

This has resulted in huge improvements in other children suffering from this incurable and debilitating disease.

And the couple is convinced that this will greatly improve Theo's quality of life.

Laura, 29, said, "The treatment is to stimulate the growth of stem cells in the brain.



Theo's two parents, Laura and Andrew, believe that pioneering stem cell surgery in Panama could improve their quality of life



Doctors fight for seven minutes to revive Theo stillborn

"For the moment, he can not coordinate his movements but it could improve. Or he could learn to speak.

"It will be small steps, but each one would be a huge step for us."

According to this procedure, 35 million stem cells from a donor umbilical cord would be injected into Theo's system to stimulate and repair damaged neural tissue in the brain.

Laura and Andy hope to take her to the Panama Stem Cell Institute once a year for five years.

Each treatment would cost around £ 16,000, but it is said that this could dramatically improve the young person's life, helping him to take important steps that he can only dream of at the moment.



His brain was deprived of oxygen and meant that he was unable to sit, walk or talk.

Laura, head of health and safety at Wirral, Merseyside, said, "About five percent of your brain is developed at the age of five. So we would like to receive the first three treatments by then so that they have the most benefits.

"There is the cost of treatment for Theo and we would also need to cover the costs of taking him with him there to treat him."

In the UK, around 30,000 children have cerebral palsy.

Some have had successful treatment with stem cells and the couple hopes the same thing will happen for Theo.

Holly Greenhow, of Cambridgeshire, made a "huge improvement" after undergoing the procedure at the age of 11 in the United States.

This allowed him to improve his vision, expand his vocabulary and better control his muscles.

Her mother, Fiona, said, "Suddenly seeing tiny steps is wonderful and it just gives us hope for what could happen in the future."



The couple is trying to raise £ 100,000 to fund various treatments to help them reach their goals

Laura said she hoped the treatment would do the same for Theo, who is 21 months old.

She said, "Theo is the biggest fighter we know. Every little thing that it does is a challenge. He has the biggest smile and is the happiest little boy.

"He deserves a chance in the life of which he has already been a victim. There are many innovative therapies and treatments. But they are not accessible on the NHS and the cost is very high. We have done so much research about it, read so many things and we know it works.

"It's just not available on the NHS. There are many places in the world that do, but not the United Kingdom.

"They have not pbaded all the clinical trials.

"Not only will he need this treatment, but he will also need specialized equipment.

"If we could go to America every year to take this treatment, it could potentially help Theo grow and perhaps even reach the key milestones that parents are so excited to see."



But her parents say that treatments that could help Theo are expensive



Doctors think that he may be suffering from quadriplegic cerebral palsy, but they will have to wait until he is two years old for the diagnosis to be complete.

The young child is thought to have tetraplegic cerebral palsy, although this can not be completely diagnosed before the age of two.

He will need an MRI to receive the complete diagnosis once he has reached the required age.

Prior to the devastating events of her birth, Laura stated that her pregnancy with Theo – her only child with her husband Andy, age 34 – was normal.

In a video that they published online, they told their friends how delighted they were with the pregnancy, sharing the scanned photo and revealing that they had discovered that they had a boy at 20 weeks old.

But at the hospital on October 18, 2017, doctors fought for seven minutes to revive Theo after he was stillborn. He also had many crises.

Laura said these factors and lack of oxygen resulted in brain damage and cerebral palsy.



Theo's parents had to wait until it was five days before they could hold their son



Theo was diagnosed with cerebral palsy at 11 months

Andy and her told how their baby was blue and that he was immediately chased away from them, describing it as their parents' worst nightmare.

After seeing him resuscitated, the baby was placed on survival devices, tied to many wires and tubes, while his father and mother were told that he might not do it.

Laura describes how she cried when she was finally able to hold her son for the first time at the age of five days.

After finally bringing him home, they quickly realized that he was not growing at the same rate as the other babies.

Cerebral palsy – which affects one in every 400 children in the UK – was diagnosed at the age of 11 months.



They want to buy an intensive hyperbaric oxygen chamber system for Theo, but it costs £ 17,000

The couple says Theo's smiling face and "contagious laughter" keep them going as they strive to raise the money they need to receive treatment abroad.

Laura said, "We just want to help her reach her full potential and have an amazing quality of life."

As part of the fundraiser, the family also wants to purchase an intensive hyperbaric oxygen chamber system for Theo.

These cost £ 17,000. Laura said: "This has the advantage of reducing swelling of the brain, but also increase the growth of stem cells in the brain to redirect signals.

"It provides 96% oxygen and can be used every day.

"You can rent them but it's too expensive. That's why we would like to buy him one. "



They hope to use some of the funds to buy special chairs and car seats for their son.

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Main reports of Mirror Online

The family will also need funds for any changes it will have to make to their home as Theo expands.

This includes specialized equipment and physiotherapy outside the NHS, special seats, car seats and wheelchairs.

Laura said, "If we can raise funds quickly enough, our son will change lives.

"Theo has already experienced so much in his life with barely a whisper of complaint, and it would be catastrophic to miss such an opportunity."

  • To help Theo and his family, click here.

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