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
  • Why Dr. Raviram S is Palakkad’s Most Trusted Laser Proctology Specialist for Piles, Fissures, and Fistulas Health
  • Delhi Highway Projects: PM Modi’s Massive INR 11,000 Cr Boost National
  • Eco-Friendly Ganpati Utsav Celebrated in Hongkong with Chocolate idols Lifestyle
  • Dr. Gunda Sapna Prakash Rao, founder & CEO of Scure Super Speciality Hospital has received the Prestigious HMTV Nari Puraskar 2023 Business
  • Ranbir Kapoor Reveals His Reasons For Playing A Double Role In Shamshera As It Premieres On Star Gold On Nov 27 Business
  • Ashay Mohile Honored for Transformative Impact in Cybersecurity, AI Innovation, and Infrastructure Security Leadership Lifestyle
  • Supreme Group Successfully Executes First NMG Railway Movement for Mahindra and Volkswagen Skoda Business
  • Meet SURAJ SINGH MAS: The Producer Creating Purpose-Driven Stories in Indian Cinema 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

  • Shipwaves Secures ₹1.56 Crore Logistics Digitalization Order from Hindalco Industries Business
  • Dosti Realty launches 56-storey residential tower ‘Dosti 604’ in Wagle Estate Business
  • Raman Preet: Fostering Future Global Business Leaders of India via Pune Institute of Business Management (PIBM) Business
  • SGCCI has organised an inspiring event to celebrate National Youth Day Business
  • Freedeem goes an extra mile to strengthen India’s retail ecosystem against the onslaught of e-commerce giants Business
  • Lubi’s new ad campaign pumps up Gujarat Titans with a powerful Force! Business

Recent Posts

  • The Quiet Confidence That Comes From Keeping Promises to Yourself
  • The Lost Art of Waiting: What We Forgot in the Age of Instant Everything
  • The Art of Doing Nothing: Why Unscheduled Time Is Becoming a Status Symbol
  • Why Everyone Is Romanticizing Ordinary Life Again
  • Advocate Aashutosh Srivastava Conferred Honorary Doctorate in Law by Washington Digital University, USA

Recent Comments

  • Unknown on Participants Reap Rewards in Wellman’s 8-Week Digital Campaign: IPL Tickets, Autographed Virat Kohli Merchandise, and More!
  • Cashfor Gold and Silverkings Brings You the Best Chance to Sell Your Gold from Your Home Lifestyle
  • Innovators building solutions to fight the Covid pandemic selected under the IAC program Press Release
  • Khadim India Ltd has registered 120% YoY growth in PAT for FY22 Business
  • From Cycle to Style- The Remarkable Journey of Vijay Garments Business
  • Thirty young authors of India get a forum to showcase literary talent at the Muskaan Litfest for Child Authors  Business
  • SM Yugan, A 12-Year-Old Remarkable Score Of 108 Out Of 125 In 66th (NSCC) Shotgun Events Press Release
  • India’s Pre-Budget 2024-2025: A Golden Opportunity for Global Collaboration in Defence and Healthcare Health
  • A chance encounter with Author, Entrepreneur and philanthropist Aditya Tikku Press Release

Copyright © 2026 Daily News India.

Powered by PressBook News WordPress theme