Be it a patient of India or Paris to cure any diseases every human needs to undergo an operation with courage and strength of character. So, why not shake a hand with Jerome Harmon suffer neurofibromatosis type 1 underwent two face transplants overview to Indian Case.
In Paris, Jerome Harmon suffering from neurofibromatosis type 1 successfully underwent two face transplant, and it’s again an innovation in science and technology. Don’t you think so?
Do you know, who is Jerome Harmon?
Salute to Jerome’s Harmon courage following his second face transplant in Paris. Luckily, he got a face of an anonymous Twenty-two years old man after his first transplant.
Doctors have praised Jerome’s “courage” and “strength of character” following his second face transplant in Paris.
He was given the face of an anonymous Twenty-two years old man after his first transplant – took place in 2010 at northern France Hospital plus ejected by his body.
Jerome spent moons in a hospital bedroom without a face, unable to observe, converse or apprehend, after his first fresh face expelled in November 2017.
The dead man’s features rushed to Paris in November, and they finally placed on Jerome’s featureless head in January 2018.
Jerome told French news agency AFP that “I feel very well in myself,” adding: “The first transplant I accepted immediately. I thought ‘this is my new face, but the process may take time.
Jerome suffers from neurofibromatosis type 1, a genetic mutation that causes severely disfiguring tumors and related complications.
A person may go into transplant rejection when a recipient’s immune system hits the transposed gland or tissue. A regular type of denial can take place many times, and the body’s ongoing immune rejoinder can deliberately harm the transplanted organ or tissue.
To try and avoid another rejection, Mr. Hamon underwent three months of blood treatment before the transplant said nephrologist Eric Thervet.
Bernard Cholley, one of the anesthetists involved in the latest operation said everyone “was blown away by Jerome’s courage, his will, his strength of character in a tragic situation.
While he was waiting he never complained, Jerome was even in a good mood,” he revealed.
Indian case of neurofibromatosis
A teenager whose rare condition has left him with a sagging face is too scared to drop his village. Bhupinder Singh, from India, lives as a recluse because he is terrified and people will stare at him and make cruel remarks.
The 16-year-old suffers from neurofibromatosis type 1, a genetic condition which causes uncontrollable growths along the nerves. Bhupinder was born with a small tumor on his right eyelid. Gradually, he grew older; his disease led his face immersed moiety part of his face. Due to which, he is unable to visualize, utter or feed himself anything.
He was shunned from school because of his unusual appearance, leaving him too scared to go the safely to his village where friends and family accept him.
‘People in my neighborhood have accepted me, but not as every human is treated equally. The way they treat is horrible! After all, I am the human being I too do have feelings.’
‘I want to live in a such a surrounding where people are ready to accept me as I am! not by judging the appearance.’
‘Although, yes its difficult to be different from others but at the same time this is what I am gifted and I am happy with it. No matter in any of the condition I am!’
‘I always try to be positive and despite whatever are my sufferings I live joyfully.’
Despite his appearance, friends say Bhupinder is just like any other energetic, teenager and has learned to love cricket. Although he can’t go to school, he reads books every day mainly preferable English language.
Being blind in his right eye, he chops the vegetables a cooks the food like a chef. If I was in his place, I might have been not able to do so. And you won’t believe his dream is to become a chef.
His mother Kaushalya Devi, 45, learned of his condition while she was pregnant.
‘Doctors had informed us about a tumor which is on his right-hand side eyelid subsequent escort of ultrasound while my pregnancy,’ she added.
‘Doctor intimated us already about the outcomes however I was in the sixth month of gestational period, and there was no way to eliminate it.’
‘Accordingly, my hubby and I decided to introduce him to this world by giving him the best possible happy life.’
‘And he had a little bump on his eyelid similar to normal kid or child. Always happy and charming.’
Ram Dayal her husband and Kaushalya, 50, for the first time took Bhupinder to the doctor when he was only seven months old. Doctors said, ‘There is no way to control the growth and operation wasn’t possible unless he turns twenty.’
They were sent back home with pills that sadly nevermore worked. However the fear turned out into reality, as Bhupinder grew up, his face started to droop so severely that he had to go through emergency surgery when he was only nine.
Bhupinder’s father said, ‘His face had dropped so drastically that we need to request doctors to do something as soon as possible. Doctors had already declared that there’s no definite assurance, but we can hope for a miracle.’
That’s adorable his parents didn’t give up for his treatment.
Later Bhupinder was admitted to the PGI (Postgraduate Institute of Medical Education and Research)- where his dad works. Surgeons urged the family to take Bhupinder to New Delhi hospitals to the specialist, but these treatments weren’t affordable for them.
Kaushalya stated: ‘We haven’t taken him to any higher hospitals because we have no reserves.’
‘Fortunately, all the surgeries had been possible at PGI because my hubby works there, due to which, we were released from paying a penny for the treatment- we are not aware at all whether he would be rid of a tumor or not.’
Bottom words: Its proud moment, the courageous personality Jerome Harmon suffers neurofibromatosis type 1 successfully underwent two face transplant overview Indian Case. In a field of face transplantation, it is a miracle. All thanks to our medical field experts.