Alpana Sharma
@alpanas16
#RareDisease #PatientAdvocate #SpinalMuscularAtrophy, Co Founder Director CureSMA Foundation India @curesmaindia & Mom fightin 4 life saving treatment 4 son
ID: 730795332670492672
http://www.curesmaindia.com 12-05-2016 16:22:39
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Can you imagine raising INR 16 crores / USD 2.1 million in 4 months for your unwell child? Cure SMA Foundation of India ๐ฎ๐ณ organised a Run / Ride for SMA on August 4, 2024 in Hyd to raise awareness on this health theme. Ms.Archana Suresh, Director T-SIG was a Guest of Honour too.
Incredible day at 2nd Run for SMA! Hundreds showed solidarity with SMA families, raising awareness for this rare genetic disorder. Together, we're making strides towards a brighter,SMA-free future. Thanks for making this event unforgettable! Archana Suresh Ramesh konanki @lokeshlingappa
With so many posts on โwomen donโt come to Indiaโ and โwomen go abroadโ, here is my own story. My daughter did her three years of graduation in Delhi. We, then, lived in a super posh colony in South Delhi. College was 15 minutes walk of which 7 mins was within colony and seven
Abhay Karandikar We hope 2 see reverse innovation in d R&D landscape dat will benefit d society especially in d healthcare sector, right frm diagnosis 2 drug discovery, treatment n beyond. DSTIndia Narendra Modi Dr Jitendra Singh Principal Scientific Adviser, Govt. of India Jonaki Sen Amitabha Bandyopadhy Director, IIT Kanpur Tata Institute for Genetics and Society, India
This is amazing! Big shoutout to Roli, and thanks so much SMA-Europe for this opportunity. A big round of applause for the talented Turkish band who brought it to life! ๐ถโจ This powerful song is symbolising unity and strength in the face of adversity! #WeAreOne Cure SMA Foundation of India ๐ฎ๐ณ