About the Fundraiser

My name is Venkateswara and my wife name is Usha Rani We Belongs to Karnool, Andhrapradesh. We need help to  Save our son life  from a rare genetic disorder, who is just 9 months old.He has a sickness called SMA(Spinal Muscular Atrophy), and it makes it hard for him to sit, breathe and move.Requires BiPAP, physiotherapy, medications, and nebulization to strive through the day

He needs a special treatment called ZOLGENSMA to stay alive, but it's very expensive, about 17.5 crore rupees

His life was supposed to be full of fun and happiness, but because of this sickness, he was in a lot of pain. He used to reach out and laugh, but now he can't do those things anymore.Parent's words - I have been by his side since day one, witnessing every milestone in his life – from his first tear to the joy of watching him kick his little legs and grasp his first toy. However, as time passes, I have seen him gradually lose his abilities. He can no longer sit, and hold up his neck, and his hands have grown weaker. It breaks my heart to witness his decline

He needs a medicine called Zolgensma to make his life. We've tried to get help from family and friends, but it's not enough. The treatment costs a lot of money, and we can't afford it on our own.We hope you can help us by giving us some money and telling others about our story. With your support, we can give Nivansh a chance to smile and be healthy again. We are determined to do whatever it takes to save him, and we need your help to make it happen.Please donate what you can, share our story and campaign link with family and friends, and together, we can make a miracle come true for the baby.