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Lydia Anggraeni Kidarsa, Injecting Power into Children with Special Needs

From childhood he was confident. The way of thinking starts from the family.

This article has been translated using AI. See Original .

By
EDNA CAROLINE PATTISINA
· 6 minutes read
Lydia Anggraeni Kidarsa
KOMPAS/EDNA CAROLINE PATTISINA

Lydia Anggraeni Kidarsa

The Bandung Institute of Technology Boulevard route witnessed the figure of Lydia Anggraeni Kidarsa who often walked up and down the campus. His baby-face smiles quickly even though his steps are always slow because he has had spinal muscular atrophy (SMA) since childhood. SMA is a neuromuscular disorder that generally causes muscles to weaken and shrink progressively.

Despite physical limitations, especially facing the stairs of the ITB General Lecture Building every day without a lift, Lydia's values ​​exceed most of her friends. This is also in addition to a plethora of activities. In one semester, she was active in 11 places with dozens of activities, such as singing practice in the ITB Student Choir, being a committee member in the Physics Engineering Student Association and Blood Donor Family, teaching tutoring at the Student Church, being a church choir, as well as visiting sick people. "In that semester, my GPA was zero decimal point," said Lydia.

Editor:
MOHAMMAD HILMI FAIQ
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