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
  • The Cinnamon Truth: Orika’s True Cinnamon Stick Offers Complete Transparency and Multitude of Health Benefits to Indian Consumers Business
  • Luxury French furniture brand Ligne Roset opens its first exclusive store in India, in association with Burgundy Brand Collective Business
  • From Law to Leadership- The Journey of Aashruti Brahmbhatt Lifestyle
  • Babu88Sports to Sponsor Telugu Warriors for CCL 2024 Press Release
  • Global Colliance honoured with Times Business Award 2023 in Surat Press Release
  • Latest Song “BIRTHDAY” From Renowned Haryanvi Producer Inderjeet Singh Rao Released On Gem Tunes Entertainment
  • Devi Mandai, An attempt to showcase the entire gamut of Bastar Tribal Culture before the world Lifestyle
  • Varmora Plastech: More Than Just Homeware – A Commitment to Family Well-Being 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

  • Shree Ramkrishna Trust to host ‘Pure Vivaah’ mass marriage ceremony on Feb 25 Business
  • India’s renowned luxury furniture brand, Durian, opens its first store in Thiruvananthapuram, Kerala Business
  • TMA and Titan CBG enter their second year of digital collaboration Business
  • Trom Industries Wins : ₹25.79 Crore Solar EPC Order in Rajasthan Business
  • Sameeksha Takke: From Social Media Influencer to Cricket Enthusiast Business
  • Revolutionizing commute technology Hyd-based start-up- SEPAL bags Rs50 lakhs funding from Peyush Bansal on Shark Tank India Business

Recent Posts

  • Diyvang People Need a Platform, Not Gifts” – Deputy Chief Minister Harsh Sanghvi
  • A Divine Celebration: Bhajan Jamming and Radhe Maa Janam Utsav with Manoj Tiwari and Kanhaiya Mittal
  • Dr. Manju Lodha Launches ATLAS SkillTech University’s ‘NextGen Women in STEM Scholarship’
  • Cash Ur Drive Wins approx. Rs. 7.17 Crore Multi-City Advertising Mandate from Leading Mobility Platform
  • COMPUTEX 2026 Brings the Global AI Ecosystem to Taipei

Recent Comments

  • Unknown on Participants Reap Rewards in Wellman’s 8-Week Digital Campaign: IPL Tickets, Autographed Virat Kohli Merchandise, and More!
  • US Cranberries Hosts Special Event with Global Brand Ambassador Chef Vikas Khanna Lifestyle
  • Women in Indian Hip-Hop Push Back Against Industry Stereotypes Entertainment
  • Car Insurance Premiums Likely to Rise on Reinsurance Costs: A Brief Account Finance
  • Global Buyers Verified by the Federation of Indian Export Organisations (FIEO) to Explore Sourcing Plastic Finished Products from India Business
  • Embelliish Unveils its First Luxury Furnishings Studio in Raghuvanshi Mills, Mumbai Business
  • TechDogs Releases Its Game-Changing 2025 Tech Trends For 30 Plus Domains Technology
  • Star Infomatic participates in Mega Cable Fest; displays its wide range of products at the exhibition Business
  • &TV’s Happu Ki Ultan Paltan’s Dabangg Jodi of Daroga Happu Singh and Rajjo visits Kashi Nagri during Dev Deepawali   Entertainment

Copyright © 2026 Daily News India.

Powered by PressBook News WordPress theme