The young girl with tumor in her face is taunted by everyone, but she has a dream (Video/Photo)

The young girl with tumor in her face is taunted by everyone, but she has a dream (Video/Photo)

  One teenage girl discovered that she had not left her house for years because she had been harassed by others by the giant tumors she had in her face. Ruby Dular, from India, has neurofibromosis, a genetic condition that causes tumors to grow along the nerves. This disease has no healing, [...]

 

One teenage girl discovered that she had not left her house for years because she had been harassed by others by the giant tumors she had in her face.

Ruby Dular, from India, has neurofibromosis, a genetic condition that causes tumors to grow along the nerves. This disease has no cure, the Periscope broadcast “Mail”.

Her parents first noticed that small clusters developed on her face when she was three years old and that her tumors grew since then.

Ruby Dular, from India, has neurofibromatosis which has ruined her life as people use her

The 18-year-old lock hers herself in at home and finds on her father, Lil Moon, who lost his right arm in work machinery to do her shopping

The young woman dreamed of getting married but believings she won't find a husband

The 18-year-old whose mother and best friend died four years ago, was constantly harassed at school, and now she fears she will never fulfill her dream of getting married.

“I have a terrible face”, she said. “I dream of other girls dressing up like a bride and getting married, but no one would want to marry this face”, she added.

When Ruby's father, Lal Moon, 68, and Shiv Dular began to notice the bumps, they took him to several doctors. But no drug they described had any effect.

Lal Muni, who lives in a small village in Lucknoa, in Uttar Pradesh, northern India, said: All the doctors in our area treated her with some drugs, but her condition deteriorated.

The death of her mother Shiv Dulari her 'faithful friend' hit Ruby hard and that is when she became a review 

Ruby strugles to see because the right side of her face has dropped. She has to live up the skin governing her eye

Surgery is an option but the tumours will grow back

They said we had no choice but to leave it that way. Then we tried some traditional drugs for more than six months, but that did nothing. So then we had no choice but to accept it.

As Ruby got older, the tumors became so large and it was difficult for her to go to school and go to market because many people noticed her situation.

No one at school would stay with me”, she said.

I was always ignored. I had no friends. They all laughed at me and laughed at me. It was very humiliating.

Dr. Jaswan Shakya, medical director and surgeon at the Sushma Coirala Memorial Hospital in Kathmandu, who has operated on many neurofibromatosis patients, said: Girl seems to be suffering from a multisystem genetic disorder that develops tumors in the nervous system./Periscopi/

 

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