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
  • Cup-ji – A Young start-up’s innovation finds its place on a Global stage Business
  • Empowering women in the construction equipment sector Business
  • Face of Panache Runway 2022 – Season 5 Lifestyle
  • Indore’s Pride: Dr. A.K. Dwivedi Brings Glory to India at International Conference in London Lifestyle
  • Meet Mohd Arbaaz Khan, the travel vlogger behind the YouTube channel Arbaaz Vlogs who has served as the ultimate inspiration for many Business
  • Who is Amitabh Bachchan’s Astrologer? Who is the Astrologer of Mukesh Ambani? – Read this to Know! Lifestyle
  • Arch College of Design collaborates with Manchester Metropolitan University, UK Business
  • Datuk (Dr) Vinod Sekhar felicitated at 22nd Asian Business and Social Forum with Bhartiya Mahantam Vikas Puraskar 2023-24 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

  • O Shreeji Dental Healthcare Launches ‘Aurradent’ – an Advanced Dental Clinic in Ahmedabad Business
  • My Interior Designers Is Giving Bangalore a Smarter Way to Discover Design Companies and Firms Business
  • Brick & Bolt, India’s leading tech driven construction company, redefines Education infrastructure construction with AI Led predictability Business
  • BNI Prometheus welcomes new leadership team Business
  • Urban Bagicha Brand is Redefining Urban Green Living with Sustainable Innovation and Community Impact Business
  • Investor Home Solutions (IHS) Sets a New Benchmark for Investor Engagement in Ultra-Luxury Real Estate Business

Recent Posts

  • Lagnam Spintex Reports Strong Q2 & H1 Fy27 Performance; Ebitda Rises 98% In Q2 And 64% In H1fy27
  • PATHVIK Launches to End Career Guesswork: Students Can Now Experience a Career Before They Choose It
  • Celebrating 20 Years of Pioneering India’s Solar Revolution: Orb Energy’s Journey
  • As India’s Top Law Firms Embrace AI, VakilPlus Wants to Bring It to Every Lawyer
  • Onward Technologies Delivers its Strongest-Ever Quarter; Total Revenue up 22.2% and EBITDA up 33.7% YoY; Raises FY27 Outlook

Recent Comments

  • Unknown on Participants Reap Rewards in Wellman’s 8-Week Digital Campaign: IPL Tickets, Autographed Virat Kohli Merchandise, and More!
  • An Evening with Krishna Lifestyle
  • Om Creations’ Smile Fest: Empowering Through Knowledge and Creativity Lifestyle
  • American NGO HOPE B~LIT distributed blankets, oral care kits and condoms on GB Road, Delhi Lifestyle
  • Framed Media Commences its Offline Journey with On-site Office at D21 Corporate Park, Dwarka Business
  • AURO University Welcomes Padma Bhushan Awardee Shri Kamlesh Patel “Daaji” for Festival of Learning 2024 Education
  • Fort City Brewing and BYG BREWSKI Brewing Company Collaborate on Limited- Edition Cold IPA Business
  • Over 1,000 participate in Kavisha UFIT Flow Fest, India’s first spin rave event more than 100 people spin at one time Lifestyle
  • ‘The Ba**ds of Bollywood’: Aryan Khan’s Debut — Glitter, Grief, Gossip & the Unfinished Story Entertainment

Copyright © 2026 Daily News India.

Powered by PressBook News WordPress theme