Skip to content
  • English
  • Business
  • Entertainment
  • National
  • Lifestyle
  • Education
Daily News India

Daily News India

Just another WordPress site

  • English
  • Business
  • Entertainment
  • National
  • Lifestyle
  • Education
  • Toggle search form
  • Para Powerlifting on a Fast Track, Chairman JP Singh Meets Uttarakhand CM, Athletes See a Bright Future Sports
  • From Crime Scene to Courtroom: How the School of Sciences at JAIN (Deemed-to-be University) Is Building India’s Next Generation of Forensic Leaders Education
  • Taylor Swift’s Showgirl Spectacle: How a 3-Day Film Event Redefined Box Office Power Entertainment
  • Parimatch Sports Partnered with SG Pipers as Sponsor for the Hockey India League 2026 Sports
  • Meet Vikrant Bhute, the visionary architect of the Deputy CM’s Nagpur bungalow revamp Lifestyle
  • Yaarioke – Ahmedabad’s First Private Karaoke Lounge Bringing Friends Closer Through Music Entertainment
  • Telecom Entrepreneur No 1 Sridhar Rao Makes a Big Impact at World Economic Forum Business
  • Tips Music unveils the devotional masterpiece “Pawan Bhakti De De Ram,” sung by the legendary Sonu Nigam and graced by Actress Anjali Sharma Entertainment

A birth defect in his spine and now a rare disease! 15-month old Nirvaan needs INR 17.5 cr to battle SMA

Posted on February 20, 2023 By

Mumbai (Maharashtra) [India], February 20: When a child is born, it is an occasion of happiness for everyone around. Sadly for the Mumbai-based Menon family, the joy lasted only for moments until they realised their beloved son Nirvaan was born with a birth defect- Congenital Scoliosis. Later during tests, he was diagnosed with a rare genetic disorder- Spinal Muscular Atrophy (SMA) – Type 2. This deadly disease has taken away his ability to eat, walk or breathe. The family has joined hands with the crowdfunding platform ImpactGuru.com and is raising INR 17.5 crores for their son’s treatment.

Nirvaan suffers from Spinal Muscular Atrophy (SMA) Type-2, and his condition is progressive, which means that with each passing day, his condition worsens. To help him battle this disorder, the gene therapy that shows hope is Zolgensma. To avail of this therapy, the child should be within the age limit of 2 years. Hence, it is necessary to fight against the clock and save Nirvaan’s life.

“Spinal Muscular Atrophy, a disease we had never heard of, has held our child under its clutches. We are more than willing to take all steps and knock at all doors that can help our Nirvaan. Because INR 17+ crores is a huge amount for any middle-class family to afford, we cannot lose our beloved child. Every contribution made will help us give Nirvaan his childhood back,” said Sarang, Nirvaan’s father.

What is SMA-2?

Spinal Muscular Atrophy – Type 2 or SMA-2 is a genetic neuromuscular disorder that affects the nerve cells that control voluntary muscles (motor neurons). If not treated, the progressive muscles become weak and eventually restrict any muscular movement. Babies with SMA-2 can sit without support. However, they cannot walk or stand unassisted.

The raised amount on Impact Guru, an online medical fundraising platform, will be used for Nirvaan’s ongoing treatment and dose of Zolgensma Therapy.

The single highest donation received on the crowdfunding campaign in INR is approximately 1 crore. All details are mentioned in the fundraiser link: (https://www.impactguru.com/fundraiser/help-nirvaan-a-menon)

If you have any objection to this press release content, kindly contact pr.error.rectification[at]gmail.com to notify us. We will respond and rectify the situation in the next 24 hours.

Business Tags:Business

Post navigation

Previous Post: ORRA Jewellery outshines all others by winning 5 million Hearts this Valentine’s Day
Next Post: Mr. Digant Sharma, CMD of Francture Brands has done Sole-tie-up with renowned Russian Refinery for Crude oil, LPG, LNG, Diesel and more

Related Posts

  • GrowthBeats organized Global Growth Accelerator Awards 2021 A
  • Redefining Success: 10 Trailblazing CEOs of 2023. Business
  • The October 2024 Launch Event of Cloveify Unveils Fashionable Clothing and Sustainable Impact Business
  • Signature Global launches ‘Prive Iconic Tower’ furnished by Armani Casa at SPR, Gurugram; eyes Rs 580 crore revenue Business
  • Factors Influencing Gold Price Hike In India As Well As The Global Market -VT Markets Business
  • Green Rosette at Raheja Viva: The most premium plots by K Raheja Corp Homes Business

Recent Posts

  • AM/NS India Leads Capability Building with BITS Pilani, Celebrates Graduation of First MBA Batch in Manufacturing Management
  • Dental Krafts Lead Advanced Dental Implants and Invisalign Treatments in Gurgaon
  • From Delhi to Los Angeles: The Indian Entrepreneur Reshaping Health Tech Investments in America
  • Plog Run at Hawa Mahal — GreenFit Foundation & Aravalli Foundation Spread Message of Cleanliness
  • Plog Run at Hawa Mahal — GreenFit Foundation & Aravalli Foundation Spread Message of Cleanliness

Recent Comments

  • Unknown on Participants Reap Rewards in Wellman’s 8-Week Digital Campaign: IPL Tickets, Autographed Virat Kohli Merchandise, and More!
  • Subhash Ghai, Rakeysh Mehra, Jackie Shroff, Divya Dutta and Ravinder Bhakar celebrate 75th Independence Day hosted by National Museum of Indian Cinema Press Release
  • Sujwel launches a new line of exquisite Kundan jewellery this wedding season Business
  • Sarveshwar Foods Signs MoU with German Firm for Advanced Rice Storage & Smoke Technology Press Release
  • Digital Declutter Checklist for 2026 Lifestyle
  • A Gala Designer Show with a LIVE performance by Shahid Mallya, Bollywood Singer Held in London Lifestyle
  • Prawaas 5.0 Sets the Stage for India’s Next Leap in Passenger Mobility Lifestyle
  • Kautilya School of Public Policy Students Grab Record Placements Education
  • Indxx Licenses India Super Consumption Index to Korea Investment Management for an ETF Technology

Copyright © 2026 Daily News India.

Powered by PressBook News WordPress theme