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
  • SurveyCXM: Helping Brands Crystalize Voice of Customer Business
  • Groundbreaking Invention by SRM University-AP Enhances Security and Efficiency in Face Recognition Technology Education
  • Emergence Of RightLand: Building the Foundation Of Sonipat’s Structured Growth Business
  • Harsh Palrecha : Prolific Young Entrepreneur And Founder Of BLAXK (Xtreme Fashion) Business
  • Startup Reporter announces list of 21 Business leaders of Rising India 2023 Business
  • Panorama Studios Invests in Rocket Reels, Fueling India’s First Original Stories Vertical OTT Platform Business
  • Subh Housing Announces Rs 200 Cr Investment in Gurugram with Spanish- Inspired ‘Seggovias’ on SPR Road Business
  • Heabal India Introduces Revolutionary “Heabal Tea Cigarette” in Delhi, Easiest Way to Quit Smoking Lifestyle

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

  • Yash Raj Films Invests in Rusk Media to Shape the Future of India’s Vertical Entertainment Economy Business
  • Shripad Upasani Named CEO of Parasnath Clinic, Targets INR 100 Cr Turnover by FY 2025-26 Business
  • Rajesh Power Services secures major orders worth Rs. 1,116 crores Business
  • Kingston Technology offers up to 60% discount for Amazon’s Great Freedom Festival Sale Business
  • Queen of the World India finale Season 3: Unleashing Glamour, Empowerment, and Uniqueness like Never Before!” Business
  • Companies to watch out for in 2022 Business

Recent Posts

  • Bharuch Gets 24×7 Neuro and Spine Super-Speciality Hospital with Advanced Robotic Rehabilitation Facilities
  • Your Company Doesn’t Have an AI Problem. It Has a Data Problem Holding Your AI Back.
  • Akhil Bharatiya Yadav Mahasangh Organises Mahaprasadi and Pure Bottled Water Distribution at Ujjain Mahakal on Nag Panchami and Sawan Somwar
  • Best Crypto Presale: AlphaPepe Leaves Pepeto and Moonberg in the Dust as Whales Rush Stage 20
  • World Talent Organization launches USA ‘The Brand Bharat’ to give Indian businesses greater global visibility

Recent Comments

  • Unknown on Participants Reap Rewards in Wellman’s 8-Week Digital Campaign: IPL Tickets, Autographed Virat Kohli Merchandise, and More!
  • Somaiya Vidyavihar University Announces New Batch for Somaiya Winter School Programme on 4th Nov 2024 Education
  • Ezeepay to Launch Doorstep Digital Services in Rural Area Business
  • Fraganta by Leena Jain Unveils Its Debut Perfume Pair – Ganga and Jogi – A Revolutionary Ode to Indian Luxury Business
  • Mitsu Chem Plast Limited Scales Up – Announces ~2,550 MT/Year Capacity Addition at Khalapur Business
  • Galgotias University, Salesforce Establish Centre of Excellence for Tableau AI Data Lab to Strengthen Industry Academia Collaboration Education
  • International Ambassador Meet 2024 hosted at Embassy of Ethiopia in New Delhi National
  • LIBERTY announced its Q2 and H1 ended 30th September, 2022 Unaudited Financial Results Business
  • Trezix launches Trezix One, a suite of AI assistants for smarter trade processes Business

Copyright © 2026 Daily News India.

Powered by PressBook News WordPress theme