Government & policy initiatives
Working hand-in-hand with government
Advocacy translated into initiatives on the ground — in partnership with state and union governments.
Everything we do falls into two streams — hands-on geriatric care for senior citizens, and national advocacy for rare-disease patients. Here's the work in motion.
We work in public-private-partnership mode, at policy level, to advance care, therapy and recognition for Haemophilia and Spinal Muscular Atrophy.
SMA is a group of hereditary diseases that progressively destroys motor neurons — the nerve cells controlling movement. OTG campaigns for access to therapy and medicines, and to keep SMA on the national health agenda.
RAISED IN THE RAJYA SABHAHaemophilia is a rare disorder in which blood doesn't clot normally due to insufficient clotting factors. OTG advocates for best-in-class care practices and reliable access to factor therapy across India.
REPORT PRESENTED TO UNION HEALTH MINISTERAdvocacy translated into initiatives on the ground — in partnership with state and union governments.
Comprehensive assistance brought to the doorstep — coordinated by one trusted team, on a single call.