'My body is becoming rocky.' Sometimes I try to catch something, I think my body is getting fragments. '

It is said by 37-year-old Asie J. Verdi, who is a rare and unhealthy disease, is making her skin as hard as rock.This disease has affected every aspect of life and doctors say that one day they can even take their lives. Speaking to the BBC, he said, 'The pain that hurts in my arm reminds me of all the time what is going on with me.'

The disease's name is slideshow and due to this, Jade uniform skin and joints are tight. It is also affecting their lungs that are going to be tougher and doctors say that their condition will be worse than ever.

The life of Virtual is a threat, and every morning they do not know what will be going to the shop on that day or even breathing.
Calcinosis in the hands Photo of copyright SCLERODERMA & RAYNAUDS UK

Apparently a look of a healthy woman. The damage to their skin is hiding under their clothing, and the worst effects from the disease are inside their body. In this situation, it is not easy for a general person to believe in their condition. Due to this disease many of his dreams are incomplete. They have stopped dreaming of marriage, children and their future, and they have only taken place in hope that there is a miracle and they get well.

But life was not always like this. In 2010, he was head of the IT sector at a Secondary School in London's suburban area sluvery and was enjoying an active and happier life.

This year, she decided to go to the Greek Islands with her best friend Caroline in the holiday. He was the only Caroline who saw the skin's unusual color and the present scores.

Initially, Vadiasi did not take these changes more seriously, but they did not know that these minor males and varieties are a tent of a serious illness.

It took three years to diagnose the illness of the patient. During this, many of them were tested and consulted with many doctors. Meanwhile, every day life became difficult for anxiety, whether it is to be a pen or to typing or lecture, it became a challenge for them.

Vermi recalls at the time that she should try to spend normal life as possible, but in the presence of joint pain, steady fatigue, frozen hands and feelings of continuous needles in the body, it is not easy. Was it

'About 18 months later, this was not enough for me. I remember that I was driving a car and suddenly I started crying, I met my doctor and clearly asked him what illness. "

Vardi says that due to this disease recently he had to revise the decision to establish a relationship. 'I am aware of my disability. I fear that I should give birth to a child and then leave it in the world. I've taught 20 thousand children in my life, but sorry, I'm afraid to become a mother myself now.

Vardi says he always smiled and started laughing. 'I like to laugh. When I entered the class, it was the first to smile. This is best for the start of the conversation. Even if I smile you feel that everything is fine. However, he also says that 'I think one day my entire body will become a stone, I will not even smile and become a statue.

Veteran physician Dr. Richard Russell says Vermi can breathe with the help of the helder and may also reduce swelling with steroids but there is no treatment for this disease.