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
  • Great Leadership, Delivering Great Results: Meet the Influential Leaders of India Business
  • Covero and FashionCart: Changing Online Shopping in India Business
  • MGM Anand Muthu’s Green Stays Vision: Zero-Waste opulence Business
  • Esskay Beauty Launches First-Ever Book on Salon Profitability at Professional Beauty Expo Business
  • Soak in the festivity with the spiritual anthem of the season: ‘BOL GANPATI BAPPA MORYA’ for Ganesh Chaturthi! Entertainment
  • A ray of hope amidst scorching heat: Ankibai Ghamandiram Gowani trust gives a new water body to Sonabhadra Business
  • Suhe Ve Vibe: Fukrey Fame Singer Gandhharv Sachdeva Recreates a Grand Punjabi Wedding with Nishant Malkani and Himanshi Khurana Entertainment
  • A hard-working youngster deserving success- Mohit Patel, founder of MP Media and Viral Icons 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

  • Airfloa Rail Technology’s FY26 Business Update and Strategic Direction Business
  • Infinium Pharmachem Limited announces its IPO for 31st March 2023, To be listed on NSE Emerge Business
  • LIBERTY announced its Q2 and H1 ended 30th September, 2022 Unaudited Financial Results Business
  • Film-E-Life! Make Your Life a Blockbuster Business
  • Finance Blocks appoints Shruti Kaushik as a Branding and Marketing Advisor Business
  • Maharashtra Govt reaffirms regulatory compliance for Laxmi Organic’s Lote facility Business

Recent Posts

  • 12 Exceptional Individuals Making a Difference
  • Sri Priyanka Geo Commex Limited IPO Currently Open – A Globally Diversified Commodity-Focused Business with Operations Across India, Morocco & Singapore.
  • Aastha Spintex Limited IPO Opens on June 29, 2026
  • Graduate to Global Finance Professional: How International Certifications Are Bridging the Skills Gap: Zell Education
  • KAI India Supports Environmental Conservation Initiative in Ladakh Through Forest Art Festival

Recent Comments

  • Unknown on Participants Reap Rewards in Wellman’s 8-Week Digital Campaign: IPL Tickets, Autographed Virat Kohli Merchandise, and More!
  • AKARA’s Comprehensive Solutions for Achieving Your Desired Body Shape Business
  • Co-Producer & Distributor Rohandeep Singh believes “LaVaste” will create a profound impact on audiences Business
  • Meet 20 Pioneering Companies Transforming the Business Landscape and Leading the Charge in 2023 Business
  • Emmadi Silver Jewellery Opens First Karnataka Store with Grand Launch Event in Malleshwaram, Bengaluru Business
  • Innovación 2026 Showcases a Powerful Culture of Innovation and Startup Thinking at the IEM–UEM Kolkata Education
  • Digital marketing is no more an option for businesses but a must: Saurabh V Gosain, Founder of Excel Range Media Business
  • Discover Unmatched Brilliance: Svaraa Jewels Unveils the SO-LIT Collection of Lab-Grown Solitaires Business
  • DayZero.ai completes the trial with 3000+ Users, 25+ Countries, 4500+ Plans in 3 weeks Business

Copyright © 2026 Daily News India.

Powered by PressBook News WordPress theme