A precious 1-year-old boy named Nivansh has been diagnosed with a rare and life-threatening genetic disorder called Spinal Muscular Atrophy (SMA) type 2. SMA weakens the muscles, making it difficult for him to walk, eat, or even breathe. There is a therapy that can assist him in regaining his strength and overcoming SMA, but it comes with an enormous price tag of 2.1 million USD or 17.5 crores INR. Fortunately, through fundraising efforts, a significant portion of the required funds has been raised. However, there is still a remaining amount of 950,000 USD needed to initiate the treatment. Your generous contribution can make a profound difference in helping Nivansh receive the care he urgently needs. Your participation in saving their child is earnestly requested.

FUNDRAISER

Nithyalatha Balaji