What is Spinal Muscular Atrophy that 18-month-old Kanav from …
Sep 13, 2023 · 18-months-old boy Kanav Jangra from Najafgarh, Delhi, is suffering from a rare genetic disease called Spinal Muscular Atrophy (SMA) Type 1. This disorder affects the motor neurons—nerve cells that control voluntary muscle movement. …
INR 80 Lakhs Raised in 80 Minutes on Impact Guru by Delhi's Jangra ...
Feb 2, 2023 · Mumbai, Maharashtra, India (NewsVoir) Delhi-based Jangra family is raising funds through India's leading crowdfunding platform ImpactGuru.com for their 11-month-old son KanavJangra who is suffering from SMA (Spinal Muscular Atrophy) Type 2. 15,000+ generous donors across India have come forward and contributed a record breaking INR 80 lakhs in 8...
Rs 80 lakhs raised in 80 minutes on Impact Guru by Delhi's Jangra ...
Feb 2, 2023 · Mumbai (Maharashtra) [India], February 2 (ANI/NewsVoir): Delhi-based Jangra family is raising funds through India’s leading crowdfunding platform ImpactGuru.com for their 11-month-old son Kanav Jangra who is suffering from SMA (Spinal Muscular Atrophy) Type 2. 15,000+ generous donors across India have come forward and contributed a record ...
Delhi’s Jangra family raising INR 17.5 crores for their ... - TechStory
Apr 13, 2023 · Delhi-based Jangra family is raising funds through India’s leading crowdfunding platform ImpactGuru.com for their 14-month-old son Kana v Jangra who is suffering from SMA (Spinal Muscular Atrophy) Type 1.
kanav jangra 18 months old kid with spinal muscular atrophy gets …
Sep 13, 2023 · Rare Deseases and Story of Kanav Jangra: 18 महीने का एक बच्चा। ऐसी दुर्लभ बीमारी का शिकार जिसके इलाज के लिए आने वाले इंजेक्शन की कीमत थी 17.5 करोड़ रुपये। पिता ने ऑनलाइन क्राउडफंडिंग का अभियान चलाया और देखते ही देखते कनव जांगड़ा की मदद के लिए डेढ़ लाख लोग आगे आ गए। आखिरकार कनव को नई जिंदगी मिल गई।.
How 1.5 lakh people collected Rs 10.5 crore to save a life of 18 …
Sep 13, 2023 · In a heartwarming display of unity, approximately 1.5 lakh people came together to support little Kanav Jangra, an 18-month-old child afflicted with the rare genetic disease known as Spinal Muscular Atrophy (SMA) Type 1.
1.5 lakh people raise Rs 10.5 crore for a shot to save Delhi kid's life
Sep 13, 2023 · Around 1.5 lakh people pitched in for little Kanav Jangra. The 18-month-old, suffering from a rare genetic disease called Spinal Muscular Atrophy (SMA) Type 1, needed one dose of an injection to survive beyond two years. The problem was, the injection, Zolgensma, costs Rs 17.5 crore.
Baby’s treatment costs Rs 17.57 cr, father looks to central govt for ...
Jan 26, 2023 · The child, Kanav Jangra, is suffering from a rare disease called SMA (Spinal Muscular Atrophy) type-1 and the treatment is an injection named Zolgensma.
Kejriwal went to meet Kanav Jangra with Arora, known health status
Sep 13, 2023 · ਅਰੋੜਾ ਨੇ ਅੱਜ ਇੱਥੇ ਇੱਕ ਬਿਆਨ ਵਿੱਚ ਕਿਹਾ ਕਿ ਕੇਜਰੀਵਾਲ ਨੂੰ ਦੱਸਿਆ ਗਿਆ ਕਿ ਦਿੱਲੀ ਵਿੱਚ ਇਹ ਪਹਿਲਾ ਮਾਮਲਾ ਹੈ ਜਦਕਿ ਦੇਸ਼ ਭਰ ਵਿੱਚ ਹੁਣ ਤੱਕ ਅਜਿਹੇ ਕੁੱਲ ਨੌਂ ਮਾਮਲੇ ਠੀਕ ਹੋ ਚੁੱਕੇ ਹਨ। ਇਸ ਮੌਕੇ ‘ਤੇ, ਕੇਜਰੀਵਾਲ ਨੇ ਇਸ ਸਾਲ ਜੂਨ ਵਿਚ 21,25,000 ਅਮਰੀਕੀ ਡਾਲਰ (ਲਗਭਗ 17.50 ਕਰੋੜ ਰੁਪਏ) ਦੀ ਕੀਮਤ ‘ਤੇ ਜੀਨ ਥੈਰੇਪੀ, ਜ਼ੋਲਗੇਨਐਸਐਮਏ (ਮੇਡ ਇਨ ਯੂਐਸਏ) ਦੇ ਇੱਕ ਪੈਕ ਦਾ ਪ੍ਰਬੰਧ ਕਰਨ ਵਿੱਚ ਕਨਵ ਦੇ …
INR 80 Lakhs Raised in 80 Minutes on Impact Guru by Delhi's Jangra ...
Feb 3, 2023 · Delhi-based Jangra family is raising funds through Indias leading crowdfunding platform ImpactGuru.com for their 11-month-old son Kanav Jangra who is suffering from SMA (Spinal Muscular Atrophy) Type 1. 15,000+ generous donors across India have come forward and contributed a record breaking INR 80 lakhs in 80 minutes i.e. INR 1 lakh raised every...