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Kerala launches crowdfunding to aid patients with Spinal Muscular Atrophy, a rare and costly disorder.
Kerala's Health Minister Veena George has urged for increased social support for patients with rare genetic disorders, particularly Spinal Muscular Atrophy (SMA), highlighting the need for community and government assistance.
To help cover the high treatment costs, which can be around Rs 13 crore per patient, the state has launched an official crowdfunding program.
SMA, a rare neuromuscular condition, affects mobility and is a significant cause of infant mortality in India, with one in 7,744 infant deaths attributed to it.
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Kerala lanza un crowdfunding para ayudar a los pacientes con atrofia muscular espinal, un trastorno raro y costoso.