Keya, an 11 year old girl born with the genetic disorder called as Spinal Muscular Atrophy, has coded her own app to share with the world how her journey has been, how she has fought it against all odds along with her mother. We hope that the app spreads the awareness about Spinal Muscular Atrophy. This app also aims to help her collect funds for her treatment and update everyone about her progress.
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