“We’re grateful for the free treatment, we couldn’t have afforded to pay for it,” said Khatun. Khatun spends her time making jewelry to earn some amount of money. As per doctor Sen, only fewer than half a dozen people all across the world are suffering from epidermodysplasia verruciformis.
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It was also observed last year that a young Bangladeshi girl was also suffering from the same kind of rare condition. The Dhaka Medical College Hospital actually treated the girl who was suffering from same condition.
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Doctors also suggested surgery on that girl. But, as per reports, her father said that barks on the body even grew in greater numbers afterwards. Her father was reluctant for the treatment and withdrew her daughter from the treatment. While doing so, he said that he doesn’t her daughter to grow up in a hospital ward.
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