When little Ved Singh turned 8 months old, his parents began noticing something unusual. Unlike other children his age, Ved was unable to sit and move normally. Worried, they took him to the doctor, hoping it was just a delay in his development. But what they heard left them shocked. Their little boy was diagnosed with Spinal Muscular Atrophy (SMA) Type 2, a rare condition that affects muscle strength and movement.
Since then, Ved's childhood has been far from normal. At just 1.5 years old, he is struggling with movements that most children learn naturally. His parents, who belong to a poor village family, have been running from pillar to post to find treatment for their son. Travelling to another state for medical consultations and treatment has only added to their difficulties.
His father, Randhir Kumar, is doing everything he can to save his little boy, but the family is struggling to arrange ₹11 crore for Ved's treatment at AIIMS, Delhi.
A child so young should not have to fight such a difficult battle, and his parents should not have to watch helplessly.
Ved needs your support to get the treatment that could change his future. Please come forward, extend a helping hand and help this little boy fight SMA.
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