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
  • GenWorks Advocates For Tackling Cardiovascular Diseases On World Heart Day Health
  • OPPO India expands its Find X9 Series with Next-Generation Imaging and AI Experiences Business
  • On This ‘WORLD CANCER DAY’: 8 Best Oncologists Share Their Advice on Increasing Risks of Cancer. Business
  • Hyder Kazmi’s multiple awards winning film ‘Jihad’ will release on the OTT platform “Mastani” on the occasion of Eid. Entertainment
  • Honorable Prime Minister Narendra Modi inaugurated the 27th National Youth Festival Business
  • Global sports Pickleball Champions 1st ever pickleball tournament with Glamour of Bollywood Business
  • Discover Unmatched Brilliance: Svaraa Jewels Unveils the SO-LIT Collection of Lab-Grown Solitaires Business
  • The Economic Times partnering with Concept Medical honours ET Business Transformation Leaders 2022 Business

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

  • Golf Swings and Money Sutras, a book that is a boon to community welfare cause Business
  • ‘Clear regulatory guidelines around crypto can boost investor sentiment.’ Business
  • Empowering India’s Fitness: Push India Push’s Push-Up Challenge Garners Prestigious Philanthropy Award Business
  • Union Minister Ramdas Athawale launched the outlet of Massimo Pizzeria Business
  • Mega events, bigger Responsibility: What the Olympics and Commonwealth Games mean for Ahmedabad Business
  • Microdigit Expands Audio Portfolio with India Launch of Two Feature-Packed Audio Products at Affordable Prices Business

Recent Posts

  • Emerald Finance Limited Delivers Strong Consolidated Q1 FY27 Results; Total Income Reaches Rs 9.44 Cr with Net Profit Surging 52.72%
  • Liotech Industries Reports 73% YoY Growth in FY26 Total Income; EBITDA Rises 58% & Net Profit Up 54%
  • Advance Technoforge Limited’s Rs.24.03 Crore IPO Opens on July 27, 2026; Fixed Price Issue at Rs. 95 Per Equity Share
  • Parul University’s Young Entrepreneur Exchange Project (YEEP) Strengthens Global Entrepreneurship Through International Collaborations
  • Streaming Stops Chasing Hits, Starts Chasing Every Taste

Recent Comments

  • Unknown on Participants Reap Rewards in Wellman’s 8-Week Digital Campaign: IPL Tickets, Autographed Virat Kohli Merchandise, and More!
  • Hillary Clinton and Jay Patel pay homage to Elaben Bhatt Business
  • QMS Medical Allied Services Ltd executes binding term sheet to acquire Saarathi Healthcare Pvt Ltd and Prometheus Healthcare Pvt Ltd Business
  • Medaz Hospital, Patna: A Leader in Neurology and Trauma Care in Bihar Health
  • Bharat Blockchain Yatra kickstarted with curtain raiser event at T-Hub, Hyderabad Business
  • R Madhavan, in partnership with VistaVerse to announce Free Movie Tickets and NFTs of Rocketry: The Nambi Effect Business
  • Iyda Payments Partners with Federal Bank for Bill Payments Services Press Release
  • PCTI-JanMitr organized a Play- ‘Ek Nayi Fauj’ at the auditorium of Deen Dayal Upadhyaya Gorakhpur University Business
  • The Ultimate Guide: To Looking and Feeling your best this Summer! Business

Copyright © 2026 Daily News India.

Powered by PressBook News WordPress theme