Govt expected to find ways to raise additional ₹1 crore needed for girl’s treatment of girl: MP HC

Indore, The Madhya Pradesh High Court on Tuesday expected the Centre and the state government to find a way to provide financial assance, considering the need for additional ₹1 crore for the treatment of a three-year-old girl suffering from ‘Spinal Muscular Atrophy Type-2’, a rare medical condition.Govt expected to find ways to raise additional ₹1 crore needed for girl’s treatment of girl: MP HCJustice Sandeep N Bhatt of the Indore bench of the HC, while hearing a petition filed three-year-old Indore resident Anika Sharma, noted that the cost of the injections required for SMA treatment is approximately ₹9.55 crore, and financial assance of up to ₹50 lakh is available under a central government scheme.Petitioner’s lawyer, Chanchal Gupta, informed the court that approximately ₹8 crore have been raised through campaigns run various non-governmental organisations and charitable institutions.He told the court that this amount is currently with the concerned institutions.The high court directed the petitioner’s lawyer to submit all the relevant details from these institutions and an affidavit stating that they are willing to pay the treatment amount to the All India Institute of Medical Sciences , New Delhi, upon the bill for the injection.The court stated that the bill from Novartis, the company that manufactured the injection, must be made available to AIIMS for necessary action.The HC noted that even after combining the central government’s assance of ₹50 lakh and the approximately ₹8 crore raised through crowdfunding, an additional amount of ₹1 crore was still needed.”It is also expected that looking to the special circumstances, the government can also find out some way to consider such cases under exceptional case to provide further financial assance which is also to the tune of ₹1 crore after adding ₹50 lakh as the government and ₹8 crore which are already collected through crowd funding various institutions,” the HC said.It is also open for the state government to find out some way to provide some financial assance. It is also expected probably the next date that the further amount can be received from other organisation/ institution so that the treatment of the said child who is suffering from rare disease can be started at the earliest.”The court has fixed the next hearing of the case on August 18.Spinal Muscular Atrophy is a genetic neuromuscular disease. In this, the motor neurons present in the spinal cord gradually get destroyed, due to which the muscles become weak and start degenerating.Motor neurons are specialised nerve cells found in the brain and spinal cord that transmit messages from the brain to the body’s muscles for various functions, including breathing, swallowing, and speaking.This article was generated from an automated news agency feed without modifications to text.