Tragedy as little boy dies of a rare cancer

We use your sign-up to provide content in ways you’ve consented to and to improve our understanding of you. This may include adverts from us and 3rd parties based on our understanding. You can unsubscribe at any time. More info

A little boy died after battling a rare cancer for months.

Fletcher Discombe, seven, developed a lump in his neck and started to lose his vision – weeks before his family had planned to emigrate to Australia.

Tests in May last year showed the youngster, affectionately known by the nickname Tigger because before he became poorly he was always bouncing around in a happy mood, had a big tumour behind his nose.

Fletcher was rushed to hospital where he spent a few weeks and underwent a gruelling but successful 15-hour operation to save his eyesight. Rhabdomyosarcoma, the rare type of cancer, had formed in soft tissue – specifically skeletal muscle tissue – and spread to his lungs and bone marrow, giving him just around 20 per cent chance of survival.

Despite his bravery and attempts at treatment, Fletcher died on November 16 with his family by his side at a children’s hospice near Bristol.

Paying tribute to her son, mum Kat told Devon Live: “Fletch was a fighter, he never complained throughout treatment. The only times he really got upset was when he was neutropenic from the chemotherapy which caused a high temperature.

“This meant trips back to the hospital for a minimum of 48 hours of antibiotics. Fletch was an absolute lover of life, he was the kindest, bravest boy who adored his sister and would often want to buy her flowers. Losing him has broken us all.”

To try and prevent further tragedies, Kat and Fletcher’s dad Tony have just launched a fundraiser called Fletcher’s Arc in association with children’s cancer charity Alice’s Arc. The charity is dedicated to finding a cure and kinder, more targeted treatments for those diagnosed with rhabdomyosarcoma.

Kat, who also has a daughter, said she and Tony “remained positive” her son could overcome the illness.

“He commenced the gruelling chemotherapy which made him very sick,” she said.

“However, we soon got into a new routine and he was able to have chemotherapy at the Royal Devon and Exeter Hospital (RD&E). We had to move in with our parents as we had sold our house and try to rebuild our lives while dealing with cancer.

“Fletch had scans after three months of treatment. We were told that the PET scan showed no evidence of disease and the tumour had almost completely gone in his head. His bone marrow was also clear. This was the best news we could have hoped for.”

Fletch started radiotherapy last September, but had been struggling to eat, swallow and talk due to suffering badly with mucositis – a common side effect of chemotherapy and radiotherapy. Despite appearing to get better, on a return trip back home from the RD&E, Fletcher had a massive seizure in the back of the car.

Kat continued: “We thought we had lost him. I called an ambulance but was told they were all busy. I drove him quickly to A&E at Torbay Hospital where he was intubated and put in the intensive care unit (ICU).

“The hospital didn’t have a paediatric ICU so they were trying to get us back to Bristol as soon as possible. After a night there, we were told Bristol didn’t have enough beds which was upsetting to hear as we felt this is where he needed to be.

“An MRI was carried out and we were told it was possibly radiotherapy side effects or meningitis. Eventually, we were transferred to Oxford as this was the only place available.

“Ironically, it was the hospital I was born in, and at least it meant we had some family close by to look after our eldest child Erin. Fletch was able to breathe on his own and seemed to respond well to us.”

However, he then suffered two more seizures, the last taking a detrimental toll on his health. Kat said: “Unfortunately, due to the fact he had had such a long seizure, he lost the ability to talk to us. After days and hours of waiting we were told the MRI scan showed evidence of cancer on his brain and spine which was causing the seizures.

“We were then taken to a side room and told there was nothing that could be done for Fletch and they would try to move him to a hospice.”

Fletcher died at Charlton Farm Children’s Hospice as his condition deteriorated.

The Arcs platform has since been created to honour children and young people’s experiences with rhabdomyosarcoma. The stories of children and young people currently fighting the disease, who have survived the disease and those who have died as a result of the disease are shared.

The Arcs enable families to come together to pool funds for research, to advocate for change and to provide a family support network.

Kat said: “We have launched Fletchers Arc under Alice’s Arc Charity to help raise awareness of Rhabdomyosarcoma and childhood cancer and to also raise money to fund vital research into this particular cancer. Unfortunately, there is only three per cent of funding allocated to children’s cancer which is just not enough.

“Any donation no matter how small will go some way to helping other children in the future.” To donate to the fundraiser please click here.

Source: Read Full Article