Six-year-old boy is battling cancer after doctor dismissed symptoms
Six-year-old boy is battling cancer after bungling doctor dismissed his symptoms as an ‘ear infection’
- The doctor in question has since been ordered to undergo further training
A six-year-old boy is battling cancer after a bungling doctor dismissed his symptoms as an ear infection, his mother has revealed.
Sebastian Nunney’s mother Lindsay was initially told that her son had probably developed an ear infection while at a GP appointment during the Covid pandemic in 2020.
But, months later the young boy was diagnosed with neuroblastoma, a rare cancer that mostly affects babies and children.
Sebastian’s family has recently launched an appeal to raise £200,000 to send him abroad for potentially life-saving therapy.
Following a complaint by the family and an investigation by the General Medical Council, the doctor in question has since been ordered to undergo further training.
Pictured: Sebastian Nunney in July 2020, after being diagnosed with a rare cancer neuroblastoma
Sebastian with his mum Lindsay and dad Gregg. The family has launched an appeal to raise £20,000 to send him abroad for potentially life-saving therapy
Lindsay, 41, who fell pregnant with Sebastian after undergoing IVF, said: ‘I was with Sebastian, he was clearly in pain and didn’t want to be examined. It was at the peak of Covid so the GP had full PPE on and I got the impression she wanted us out of there as quickly as possible.
‘At the time, doctors did not want to do face-to-face consultations but we really pushed for it because Sebastian had lost a lot of weight. I even showed her photographs of Sebastian just a few weeks earlier to try and show her how much weight he had lost.
‘The doctor actually said it could be an ear infection because there was some inflammation in the ear.
‘She read in the notes there had been a referral to see a paediatrician because Sebastian could be on the [autism] spectrum and she said “oh yes I see there might be some behavioural problems”.’
Weeks later in July 2020 his parents took him to hospital after he became increasingly weak and tests showed his oxygen levels were dangerously low.
He had an X-ray which showed a large mass in his chest and further tests revealed he had the rare cancer neuroblastoma.
Sebastian was rushed to the Queen’s Medical Centre in Nottingham and placed on a ventilator and underwent a tracheostomy so a tube could be inserted into his windpipe.
Sebastian has neuroblastoma which is a rare cancer that mostly affects babies and children
The six-year-old has received treatment at Queen’s Medical Centre in Nottingham
Sebastian’s mother said his weight had plummeted and he complained of an ‘ear infection’
Father, Gregg, 43, said: ‘At the very beginning he was very sick.
‘One Friday we were told by the nurses that we were allowed to be together at his bedside – even though Covid restrictions said we couldn’t – “to make things more manageable”, but we were told afterwards it’s because they didn’t expect him to make it through the weekend.’
They took turns on the bedside vigil where a heavily sedated Sebastian was started on a gruelling 80-day chemotherapy programme.
Gregg said: ‘He looked like Doctor Octopus with all these tubes and wires. Nobody thought he was coming out of PICU.
‘They took us to the room of doom again and said, “he’s never coming out”. We were just numb at that moment.’
Despite the odds being stacked against Sebastian, the brave youngster battled back and his tumour shrunk so much that doctors hailed it a ‘miracle’.
But earlier this year, doctors discovered a cancerous growth in his leg and blood tests revealed the disease may have returned.
Mother Lindsay (pictured) was initially told her son, who was three years old at the time, had probably developed an ear infection, whilst at a GP appointment in 2020
In July 2020 Sebastian’s parents took him to hospital after he became increasingly weak and tests showed his oxygen levels were dangerously low
Sebastian’s dad Gregg compared his son to Doctor Octopus due to the tubes and wires attached to him
Gregg said: ‘At the end of May Sebastian was still suffering – he was sore and tired – very upset and falling asleep at school, refusing to eat.
‘It felt very much like his symptoms when he was first diagnosed.
‘We were reassured that this was just his response to the radiotherapy, that he was just fed up after three years of treatment, and to just let him rest.
‘He was in so much pain he just wanted to sleep and cry all the time.
‘An MRI scan on June 20 showed abnormal tumours in his pelvis, the base of his skull and the soft tissue around his eyes.
‘At the point we got the results, we were basically told that there isn’t much hope now and we will try and find something to manage his pain.
‘Our consultant said we’re running out of options in terms of quality of life over treatment.’
The family, from Kettering, Northants, has launched an appeal to raise £200,000 to send Sebastian abroad for potentially life-saving therapy
In July 2020, Sebastian had an X-ray which showed a large mass in his chest and further tests revealed he had the rare cancer neuroblastoma
While undergoing treatment on the NHS, the family, from Kettering, Northants, have launched an appeal to raise £200,000 to send Sebastian abroad for potentially life-saving therapy.
One of the therapies the couple are looking into is CAR-T cell therapy which is available in Italy and America.
It works by collecting a patient’s white blood cells, editing them in a lab to seek and destroy tumour cells, then injecting them back into the body.
To donate to Sebastian’s GoFundMe click here.
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