FOR six years Prosper has lived with a life-threatening tumour engulfing his face
The big mbad robbed him of his sight, left him struggling to breathe and drove his personal mom to disown him, leaving simply his father to look after him.
Kambou Sie, in any other case know as Prosper, from Bondoukou, Ivory Coast was 11 when the aggressive tumour first appeared on his cheek.
But, left untreated, it has grown slowly, utterly swamping his facial options.
Doctors initially thought it was a non-cancerous tumour however checks when he lastly reached hospital this yr revealed it was a uncommon type of the illness.
Prosper mentioned: “People mentioned I used to be some type of monster, saying that perhaps it was one thing I had eaten which made me like this, however my cheeks simply saved getting greater and greater.”
Nobody might perceive what was taking place to Propser’s face and with no cash to help him, his mom struggled to manage.
Prosper mentioned: “When I turned in poor health, everybody mentioned that I might not be healed or liked, so she stopped caring about me and taken care of her different kids as a substitute.
“When the disease got worse, everybody left me. My father was the only one who looked after me.”
Desperate for badist, Prosper’s father contact Sister Claudine from the Liliane Foundation, a charity that specialises treating disabled kids from creating international locations.
The nun put Propser involved with the Italian charity A Voice For Padre Pio, which offers social and medical help, and collectively they made an attraction video to obtain badist.
The charity flew him to Naples Pascale Hospital in Italy, to seek out the badysis he had been ready six years for.
Prosper mentioned: “When individuals see me, they are saying they’ve by no means seen this illness on anybody else. I couldn’t keep on dwelling.
When I turned in poor health, everybody mentioned that I might not be healed or liked, so she (his mum) stopped caring about me and taken care of her different kids as a substitute
“I hope to be cured, even when I’ve to undergo first.
“The main thing I want to come from this is to get my cheeks sorted.”
Samples of tissue have been faraway from Propser’s face, to determine the reason for the illness and an acceptable therapy.
Prosper was initially referred to the hospital with a tentative badysis of neurofibromatosis, nonetheless docs have been shocked to seek out an extremely uncommon type of most cancers – Burkitt lymphoma.
What is Burkitt lymphoma?
Burkitt lymphoma is a type of non-Hodgkin’s lymphoma through which most cancers begins within the immune cells.
It is known as after British surgeon Denis Burkitt, who first recognized the illness in 1956 amongst kids in Africa.
It is widespread in younger kids who’ve malaria and Epstein-Barr virus, a standard virus that additionally causes glandular fever.
It happens when the physique’s immune cells begin attacking itself.
Burkitt lymphoma is unusual – about 210 persons are recognized with any such lymphoma yearly within the UK.
The commonest symptom is a number of lumps that develop shortly.
It is the quickest rising human tumour and is deadly if left untreated.
But intensive chemotherapy can enhance survival charges.
As therapy is intense sufferers are prone to want to remain in hospital whereas present process therapy.
The illness badaults wholesome cells which are working within the immune system.
In most circumstances like Prosper’s, it’d be deadly if left untreated.
Hematologist Dr Ferdinando Frigeri mentioned: “The prognosis we expect to see is that we’re coping with a cancerous tumour.
“The most distinction facet we’ve seen is that the speed of pace of development is far slower than one usually related to Burkitt lymphoma.”
Prosper underwent a mix of chemotherapy, radiotherapy, stem cell substitute to cut back the tumour.
Once accomplished, he can have beauty surgical procedure to take away the lifeless tissue in his face.
During his therapy Prosper obtained an emotional message and apology from his estranged mom.
And after months of aggressive therapy, scans confirmed that Propser’s facial swelling had diminished important, even permitting his eyes to open.
He mentioned: “At the beginning my face was so huge, I could not do something. But now I thank God.
“I’ve almost completed my chemotherapy and every little thing has deflated. My face is a lot better.”
Prosper’s story is featured on Body Bizarre, together with a pair of brothers whose uncommon situation means they lose bone faster than they develop, and a Brazilian boy born with no eyes.
The episode may even function a British couple who handed on Treacher Collins Syndrome to their daughter and Heitor, the conjoined twin whose brother died after separation surgical procedure.
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