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Nepali Congress MP Pratima Gautam has demanded the government to implement the legal system related to free treatment of hemophilia.
Speaking at zero time in the House of Representatives meeting on Monday, MP Gautam said that among the ten categories of disabilities classified by the Rights of Persons with Disabilities Act, 2074 and Regulations, 2077, hemophilia is also included in one category, and that people suffering from this disease are provided free of charge medicines that they use regularly through the relevant local level, but they are not getting such facilities.
'On the one hand, the patients are suffering excruciating pain due to the inability of the state to provide medicines, on the other hand, the disability and death rate of the patients is also increasing,' she said, 'Even though there is a clear provision even in the law, it is unfortunate that the people die prematurely because of the failure to implement it. The government should save the lives of its citizens by providing anti-hemophilic factor, a drug that hemophilia patients have to use for life.'
Hemophilia is a genetic disease. When a patient suffering from this disease bleeds in any part of the body, the blood does not stop. If not treated in time, the patient will die. According to MP Gautam, the last 2 2 patients have died from this disease in the month. The number of hemophilia patients in Nepal is 4 thousand 937 people.
