On World Rare Diseases Day, India’s focus is on the high cost of treatments for rare diseases due to monopoly drug pricing. The National Policy for Rare Diseases aims to lower costs and promote local drug manufacturing. A patient’s court battle for affordable SMA treatment highlights the need for policy implementation and transparent drug pricing. Post navigation BRO camp buried in Uttarakhand avalanche, warning was issued on Thursday evening – Top updates ‘Identify, deport illegal intruders’: Amit Shah reviews Delhi security, orders strict action on infiltration, crime control