i M POSSIBLE!
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i M POSSIBLE!
Signed in as:
filler@godaddy.com
CROWDFUNDING STORY
DANCING ON MY WHEELS WINS AT NYAF 2023
MOTHER & DAUGHTER JOURNSEY
COCONUT CHATS
UNIMO
WE ARE SPINE
21K SCHOOL
MUMBAI FILM COMPANY
ATHARV ABILITY
BRIBOOKS
Listen to this intriguing and educational chat, our Radio Icon Hrishikesh Kannan (Hrishi K) had on the #GoodMorningMumbaishow, with a team of renowned medical experts : Dr. Anaita Udwadia Hegde, Dr. Abhay Nene & Dr. Snehal Deshpande.
Do tune in and listen to this super interesting and entertaining chat between RJ Annie, my little Rockstar daughter, Keya and Me, on the #AfternoonswithAnnie show. What to expect? What does Keya like, who is Keya and some insight on Spinal Muscular Atrophy
#saturdaynoonlivewithtara … " We spoke of #teenage years and more Thanks for joining @mon.ishaa for joining me impromptu "
......Tara Sharma Saluja
"What a moving chat this was... thanks for joining #saturdaynoonlivewithtara and Monisha gosh you are so strong practical and amazing as are your kids @keya.battles.sma
Please watch and please let us all help them however possible."
.....Tara Sharma Saluja
Hyderabad Premiere Golf League, is doing something a little different this year. They want to take a few minutes of your time to tell you about a little girl, Keya. Please watch and share the video, spread awareness, donate, and let’s all work together to help Keya fight SMA 🙏! Keya Battles SMA with HPGL.
Copyright © 2022-2024 - KEYA FIGHTS SMA - All Rights Reserved.
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