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Families of children with rare diseases in India are abandoned by policymakers and society
All that the government has offered the vast majority of rare disease patients is a crowdfunding platform where they can make a request for donations.
United states
Justice prathibam singh
Nidhi shirol
Justice singh
Sanofi genzyme
Rashtriya arogya nidhi
Prasanna shirol
Meryl mammen
Alok bhattacharya
Andhra pradesh chittoor
Shilpi bhattacharya
Organisation for rare diseases india
Drug administration
Ministry of health
Indira gandhi institute of child health
Ashoka university
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