New Delhi, Sept. 25 -- The mother of a two-year-old child with Spinal Muscular Atrophy (SMA) Type 1 had been sitting outside the All India Institute of Medical Sciences (AIIMS) in south Delhi for days, asking for help to get her daughter treated for the disease.

While many passed by without a second glance, social media influencer Sunny Mahor (@thodakhalo), known for his community outreach, approached her with his team. He quickly began rallying the crowd, showing medical records to passersby and explaining the specific injection the child urgently needed.

SMA Type 1 is a rare genetic disease affecting a child's central nervous system, severely restricting voluntary muscle movement. According to the child's mother, she needs an injectio...