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Parents of children suffering from DMD stage protest at Jantar Mantar

The parents of children suffering from Duchenne Muscular Dystrophy (DMD), a fatal genetic disease, gathered at the Jantar Mantar on Friday to raise awareness about the disease and register their dissent against the government's apathy.The . ....

New Delhi , Sheffali Gulati , National Policy For Rare Diseases , Duchenne Muscular Dystrophy , Jantar Mantar , National Policy , Rare Diseases , Save Our Son ,

Parents Of Children Suffering From DMD Stage Protest At Jantar Mantar

New Delhi, March 24 (IANS) The parents of children suffering from Duchenne Muscular Dystrophy (DMD), a fatal genetic disease, gathered at the Jantar Mantar on ....

New Delhi , Sheffali Gulati , National Policy For Rare Diseases , Duchenne Muscular Dystrophy , Jantar Mantar , National Policy , Rare Diseases , Save Our Son ,

Parents of children suffering from DMD stage protest at Jantar Mantar

Parents of children suffering from DMD stage protest at Jantar Mantar
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Sheffali Gulati , National Policy For Rare Diseases , Duchenne Muscular Dystrophy , Jantar Mantar , National Policy , Rare Diseases , Save Our Son ,

Delhi HC directs to hold meeting on issue of funding of clinical trial for rare diseases

The Delhi High Court on Monday directed the national consortium of concerned departments to hold a meeting and give its recommendations on the funding of clinical trials for rare diseases including Duchenne Muscular Dystrophy (DMD). ....

Justice Prathibam Singh , Sheffali Gulati , Delhi High Court On , Delhi High Court , Health Ministry , National Consortium For Research , Duchenne Muscular Dystrophy , Prathibam Singh , National Consortium , Ews India ,