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
  • Harshdeep Hortico Reports Strong H1 FY26 with Net Profit of INR 5.7 crore Business
  • Patel Retail Strengthens MMR Presence; Launches 48th Store in Mumbai Suburb Business
  • Meet Amit Kakkar: One Consultant’s Mission to Build Bridges, Not Just Careers Lifestyle
  • XLRI Jamshedpur announces admissions to 47th batch of Postgraduate Certificate in Business Management Education
  • Kaapi Solutions partners with Rocket Espresso to sell Handmade Italian espresso machines in India Business
  • How BBNC.IN Has Become One Stop Solution for Business Owners Business
  • Operated by Renowned Dr Ashwani Bansal, Chief Cardiac Surgeon Indus International Hospital; First Time of its this kind in North India Health
  • Pravesh Lal Yadav, Neelam Giri Starrer Producer Mukesh Giri’s Bhojpuri Film ‘Just Married’ Ready For Release 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

  • Punjab’s Urban Lifestyle Gets a Makeover: Residential Trends Fuel Next-Gen Housing Growth Business
  • Sakshi Chandraakar: A Beacon of Hope in the Professional Landscape Business
  • Best Crypto Presale: AlphaPepe Hits 5000 AI DEX Users Despite Market Dips As 100x Watchlist Status Grows Business
  • AVRO India 9MFY23 Net Profit upa 253% Business
  • From C Prompt to CPrompt 2.0: Powering Tomorrow with Purpose Business
  • Dr. Sahil Kadari – the power behind Bitica Blockchain Technology Business

Recent Posts

  • Best Crypto Presale: AlphaPepe Targets 300x Potential as Hunter Meme Coin Plunges From $222 to Below $2
  • Duroply launches DURO HDMMR™ – High Density Max Moisture Resistant Engineered Board
  • SBICAP Securities Limited, in partnership with Appreciate, gives investors access to Global Markets powered by India INX GA and NSEIXGA
  • Wizz partners with Appreciate to enable seamless global Investing through Wizz Financial App
  • Patil Automation Board Approves Rs 96.38 Crore Preferential Fund Raise

Recent Comments

  • Unknown on Participants Reap Rewards in Wellman’s 8-Week Digital Campaign: IPL Tickets, Autographed Virat Kohli Merchandise, and More!
  • Celebrity Hair Transplant: You’d Never Guess They Had a Hair Transplant- But They Did Lifestyle
  • Embodying Togetherness and Care: Varmora Plastech’s Products Resonate with the Needs of Every Family Member Business
  • Jindal Mobilitric Unveils EV (Electric Vehicle) With An Impressive 165 Km Range Business
  • Celebrating Gurbaani Shaiba’s Extraordinary Success with- House of Saffron Baanishaa Business
  • The Last Call Of A Country Gentleman: Why Alan Jackson’s Farewell Is Bigger Than A Concert Entertainment
  • Sonia Agarwal Bajaj Launches Little Future Founders, India’s First Financial Literacy and Entrepreneurship Program for Kids Aged 7-12 Business
  • Namaste Production Presents Udit Narayan and Aditya Narayan Live in Concert, Organized by Ekataa Theater and Hosted at Sri Shanmukhananda Chandrasekarendra Saraswathi Auditorium Entertainment
  • Insights from Leading Health Experts on World Health Day 2024: My Health, My Right Health

Copyright © 2026 Daily News India.

Powered by PressBook News WordPress theme