A challenge to the medical world! The body of a 14-year-old girl in Chhattisgarh is turning to stone, what is the exact name of this rare disease?
- Rajeshwari suffers from a very rare skin disease that causes thick, scaly patches on the skin.
- Hardening of the skin makes it difficult to walk, sit and even perform simple tasks.
- So far there is no permanent cure for this disease.
Childhood is considered a beautiful period of life for everyone but for a 14-year-old girl from Chhattisgarh, her childhood became a story of pain, suffering and loneliness. Unique to a toddler illness Her skin is gradually becoming hard as a stone. A spiky, rough layer has formed on her body. This incident, which seems to be imaginary, is happening in reality and this case has lost everyone’s sleep at present. A disease in which our body turns to stone is not convincing but in reality it is true. Let’s know about it in detail.
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The case concerns Rajeshwari, a young woman from a very poor family in a remote tribal area of Chhattisgarh. According to reports, she is approximately 14 years old. The family explained that Rajeshwari started experiencing this serious skin disease at a very young age, but due to limited resources and lack of information, she could not get timely and proper treatment. As she grew older, her skin became more and more rigid. Today, a thick layer has formed on her arms, legs and various parts of her body, making it difficult for her to walk, let alone perform simple tasks.
Rajeshwari’s illness has not only crippled her body but also deprived her of her social life. Many people in the village believe that the disease is contagious, so no one goes near her. Going to school, playing with friends and laughing freely has become a dream for her. The family says the pain makes bathing, dressing and even sitting difficult. The effects of constant neglect and isolation are evident on her mind. Due to this disease, Rajeshwari is not only physically but also mentally ill.
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Her story has gone viral on social media and has shocked everyone. This has raised questions about help and treatment. Experts say the disease is rare and genetic, with no permanent cure. However, proper care, regular medication and special skin care can reduce the pain which will make her life a little easier. What is needed more than illness is awareness, timely medical help and social sensitivity so that no other child struggles alone. Keeping everyone away from them and making them feel alone is nothing short of cruel. In the medical field, this condition is called ichthyosis hysterics. It is a very rare genetic skin disease that develops slowly over the years after birth.
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Symptoms of ichthyosis hystrix disease
- Appearance of thick, scaly, scaly patches on the skin.
- The skin becomes very hard and rough.
- Loss of flexibility in hands, feet and joints.
- Constant pain and burning due to deep fissures.
- Abnormal changes in nails and hair.
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