i M POSSIBLE!

Keya Fights SMA
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Keya Fights SMA

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I M POSSIBLE & SMAART

An initiative inspired by Keya, a proud  recipient of the prestigious Pradhan Mantri Rashtriya Bal Puraskaar. Keya's contribution to society has been recognized for raising awareness about rare diseases, importance of  their prevention and her advocacy for INCLUSION.

Keya believes "I M Possible", inspiring us to do so.

About IMPS

RARE DISEASE AWARENESS PLATFORM

ALL DONATIONS ARE COLLECTED VIA PARTNER NGO'S AND DONATED DIRECTLY TO SMA PATIENT FAMILIES.  CONTACT US FOR MORE DETAILS.

INCLUSION PARTNERS

PATIENCE ! PERSEVERANCE ! DETERMINATION ! & HOPE ! EVERY SMA CHILD LIKE KEYA DESERVES ONE SHOT TO LIFE ! TOGETHER WE CAN MAKE IT HAPPEN !

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I M POSSIBLE !

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" I M POSSIBLE ! "

KEYA HATKAR


14-year-old Keya is the recipient of the prestigious Pradhan Mantri Rashtriya Bal Puraskar 2025. She is a national & global award winning, young Author of 3 best sellers from Mumbai, India.  Keya is one of the top 30 Global Disability Inclusion Advocates, a TEDx Speaker,  self trained hand & digital Artist, Coder, Podcaster & a YouTuber.  


Born with a terminal, progressive, genetic disorder called SMA, Keya has proved over time that SMA does not define her and she inspires others. 


Her non-profit initiative, I M POSSIBLE & SMAART, advocates for inclusion of rare disease warriors

Keya's books