Muscular
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{
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75-Year-Old Elderly Man In China Becomes Beauty Influencer To Raise Money For Grandson's Rare Disease Treatment
- Saturday June 27, 2026
- Offbeat | Edited by Astitva Raj
Zhu Yunchang became a beauty influencer to raise money for his nine-year-old grandson Cao Jingyan, who has a rare disease.
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www.ndtv.com
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Chennai Construction Worker Builds Muscle On High-Carb Diet, White Rice, And 5-Day Workout: "No Idli, Dosa"
- Sunday April 19, 2026
- Lifestyle | Written by Krati Purwar
The Chennai construction worker revealed that he eats non-vegetarian food only once a week, but makes sure to include rice with sambar, rasam, and curries loaded with vegetables
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www.ndtv.com/lifestyle
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'Not Money, But Dignity': Top Court To Comic Samay Raina On Disability Jokes
- Thursday November 27, 2025
- India News | Reported by Nupur Dogra, Edited by Saikat Kumar Bose
The Supreme Court today asked comic Samay Raina to consider hosting a show with those suffering from Spinal Muscular Atrophy to spread awareness about the condition
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www.ndtv.com
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Baby Successfully Treated For Deadly Motor Neuron Diseases While Still In Womb
- Saturday February 22, 2025
- Science | Edited by Abhinav Singh
The mother took the drug daily for six weeks while the baby herself was given the drug orally, roughly one week after the birth.
-
www.ndtv.com
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Mumbai Woman Praises IndiGo For Ensuring Smooth Travel With Wheelchair-Bound Daughter
- Sunday January 26, 2025
- Feature | Edited by Anjali Thakur
In a LinkedIn post, Monisha shared the challenges of travelling with her 14-year-old daughter, Keya, who has Spinal Muscular Atrophy (SMA).
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www.ndtv.com
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What Is Spinal Muscular Atrophy? Understanding The Signs, Complications, And Treatment
- Wednesday November 6, 2024
- Health | Aayushi Singh Chauhan
Understanding the early signs, potential complications, and available treatments for Spinal Muscular Atrophy can be crucial in managing the condition and improving the quality of life for those affected.
-
www.ndtv.com/health
-
Woman Body-Shamed For "Muscular Photo" Responds To Trolls, Says "I Can't Believe..."
- Friday May 17, 2024
- Offbeat | Edited by Bhavya Sukheja
A Delhi-based fitness coach who was trolled online for sharing a muscular photo of herself has responded to bullies with a powerful post.
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www.ndtv.com
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Pfizer Pauses Gene Therapy Trial For Muscle Disease After Death
- Wednesday May 8, 2024
- World News | Damian Garde, Bloomberg
Pfizer Inc. paused a study of an experimental gene therapy for muscular dystrophy after a child who received it died suddenly.
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www.ndtv.com
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Siddaramaiah Writes To PM, Seeks Help For Treatment Of 15-Month-Old Boy
- Thursday November 2, 2023
- India News | Asian News International
Karnataka Chief Minister Siddaramaiah has reached out to Prime Minister Narendra Modi, seeking help for the medical treatment of a 15-month-old boy with a rare disease.
-
www.ndtv.com
-
Delhi Court Notice To Centre On Request Of Boy Suffering From Rare Disease
- Friday March 24, 2023
- India News | Asian News International
The Delhi High Court today issued a notice to the Central Government on a plea moved by an 11-year-old child suffering from the rare disease Duchenne Muscular Dystrophy (DMD).
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www.ndtv.com
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5-Month-Old's Medicine Costs Rs 18 Crore, Father Approaches High Court
- Tuesday February 22, 2022
- Kerala News | Press Trust of India
The Kerala High Court has sought response of the state government on a plea seeking medical assistance for a five month old baby suffering from spinal muscular atrophy (SMA) for which the medicine costs around Rs 18 crore.
-
www.ndtv.com
-
Bengaluru 10-Month-Old Awaits World's Most Expensive Injection To Survive
- Monday July 12, 2021
- India News | Written by Maya Sharma
A 10-month-old in Bengaluru, Karnataka, is fighting for her life as she waits for a medicine that costs a whopping Rs 16 crore. Diagnosed with Spinal Muscular Atrophy, type 1, the child, Khyati, needs the medicine for gene therapy before she turns 2.
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www.ndtv.com
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People Raise Rs 18 Crore To Save Kerala Child From Rare Disease
- Tuesday July 6, 2021
- Kerala News | Press Trust of India
In a display of human kindness for a cause of serious concern, Rs 18 crore was raised in Kerala through crowdfunding in seven days for an 18-month-old child suffering from a rare genetic disorder called spinal muscular atrophy.
-
www.ndtv.com
-
People Donate Rs 16 Crore For Mumbai Child Who Needed Most Expensive Drug
- Friday May 7, 2021
- Mumbai News | Reported by Sunilkumar M Singh, Edited by Divyanshu Dutta Roy
Paying Rs 16 crore for one injection may seem like an impossible task for most people but that is exactly what the parents of a five-month-old boy in Mumbai have managed to do.
-
www.ndtv.com
-
75-Year-Old Elderly Man In China Becomes Beauty Influencer To Raise Money For Grandson's Rare Disease Treatment
- Saturday June 27, 2026
- Offbeat | Edited by Astitva Raj
Zhu Yunchang became a beauty influencer to raise money for his nine-year-old grandson Cao Jingyan, who has a rare disease.
-
www.ndtv.com
-
Chennai Construction Worker Builds Muscle On High-Carb Diet, White Rice, And 5-Day Workout: "No Idli, Dosa"
- Sunday April 19, 2026
- Lifestyle | Written by Krati Purwar
The Chennai construction worker revealed that he eats non-vegetarian food only once a week, but makes sure to include rice with sambar, rasam, and curries loaded with vegetables
-
www.ndtv.com/lifestyle
-
'Not Money, But Dignity': Top Court To Comic Samay Raina On Disability Jokes
- Thursday November 27, 2025
- India News | Reported by Nupur Dogra, Edited by Saikat Kumar Bose
The Supreme Court today asked comic Samay Raina to consider hosting a show with those suffering from Spinal Muscular Atrophy to spread awareness about the condition
-
www.ndtv.com
-
Baby Successfully Treated For Deadly Motor Neuron Diseases While Still In Womb
- Saturday February 22, 2025
- Science | Edited by Abhinav Singh
The mother took the drug daily for six weeks while the baby herself was given the drug orally, roughly one week after the birth.
-
www.ndtv.com
-
Mumbai Woman Praises IndiGo For Ensuring Smooth Travel With Wheelchair-Bound Daughter
- Sunday January 26, 2025
- Feature | Edited by Anjali Thakur
In a LinkedIn post, Monisha shared the challenges of travelling with her 14-year-old daughter, Keya, who has Spinal Muscular Atrophy (SMA).
-
www.ndtv.com
-
What Is Spinal Muscular Atrophy? Understanding The Signs, Complications, And Treatment
- Wednesday November 6, 2024
- Health | Aayushi Singh Chauhan
Understanding the early signs, potential complications, and available treatments for Spinal Muscular Atrophy can be crucial in managing the condition and improving the quality of life for those affected.
-
www.ndtv.com/health
-
Woman Body-Shamed For "Muscular Photo" Responds To Trolls, Says "I Can't Believe..."
- Friday May 17, 2024
- Offbeat | Edited by Bhavya Sukheja
A Delhi-based fitness coach who was trolled online for sharing a muscular photo of herself has responded to bullies with a powerful post.
-
www.ndtv.com
-
Pfizer Pauses Gene Therapy Trial For Muscle Disease After Death
- Wednesday May 8, 2024
- World News | Damian Garde, Bloomberg
Pfizer Inc. paused a study of an experimental gene therapy for muscular dystrophy after a child who received it died suddenly.
-
www.ndtv.com
-
Siddaramaiah Writes To PM, Seeks Help For Treatment Of 15-Month-Old Boy
- Thursday November 2, 2023
- India News | Asian News International
Karnataka Chief Minister Siddaramaiah has reached out to Prime Minister Narendra Modi, seeking help for the medical treatment of a 15-month-old boy with a rare disease.
-
www.ndtv.com
-
Delhi Court Notice To Centre On Request Of Boy Suffering From Rare Disease
- Friday March 24, 2023
- India News | Asian News International
The Delhi High Court today issued a notice to the Central Government on a plea moved by an 11-year-old child suffering from the rare disease Duchenne Muscular Dystrophy (DMD).
-
www.ndtv.com
-
5-Month-Old's Medicine Costs Rs 18 Crore, Father Approaches High Court
- Tuesday February 22, 2022
- Kerala News | Press Trust of India
The Kerala High Court has sought response of the state government on a plea seeking medical assistance for a five month old baby suffering from spinal muscular atrophy (SMA) for which the medicine costs around Rs 18 crore.
-
www.ndtv.com
-
Bengaluru 10-Month-Old Awaits World's Most Expensive Injection To Survive
- Monday July 12, 2021
- India News | Written by Maya Sharma
A 10-month-old in Bengaluru, Karnataka, is fighting for her life as she waits for a medicine that costs a whopping Rs 16 crore. Diagnosed with Spinal Muscular Atrophy, type 1, the child, Khyati, needs the medicine for gene therapy before she turns 2.
-
www.ndtv.com
-
People Raise Rs 18 Crore To Save Kerala Child From Rare Disease
- Tuesday July 6, 2021
- Kerala News | Press Trust of India
In a display of human kindness for a cause of serious concern, Rs 18 crore was raised in Kerala through crowdfunding in seven days for an 18-month-old child suffering from a rare genetic disorder called spinal muscular atrophy.
-
www.ndtv.com
-
People Donate Rs 16 Crore For Mumbai Child Who Needed Most Expensive Drug
- Friday May 7, 2021
- Mumbai News | Reported by Sunilkumar M Singh, Edited by Divyanshu Dutta Roy
Paying Rs 16 crore for one injection may seem like an impossible task for most people but that is exactly what the parents of a five-month-old boy in Mumbai have managed to do.
-
www.ndtv.com