"Thank you Chris Mallika Bhadra for lending your amazing platform Coconut Chats to help me share my story and inturn help raise awareness for #spinalmuscularatrophy which has affected my little girl Keya Hatkar " ... Monisha
Single mother Monisha and rockstar SMA Warrior Keya talk about their journey in #BattleAgainstSMA . Monisha and Alpana Sharma, Co Founder of Cure SMA Foundation India join hands as they believe only #togetherwecan. Thank You RJ Annie for supporting our #Cause
"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
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.
Thank you Pluc.tv for featuring Keya's story and helping us spread the word.
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
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 and Cure SMA Foundation India
Copyright © 2022-2024 - KEYA FIGHTS SMA - All Rights Reserved.
In spite of her SMA , Keya believes I M POSSIBLE!
13 year old Keya is a national award winning author of two best sellers, an artist, coder, motivational speaker, YouTuber, podcaster and singer.
Keya's book links:
DANCING ON MY WHEELS & I M POSSIBLE!
Don't miss out Keya's recently launched new podcast series :
Keya's life-saving SMA treatment costs INR 80 lacs / year for life. Her mother needs your support to access this treatment. Keya has been receiving treatment since Jan 2022 thanks to all her donors.