Cure SMA Foundation of India ๐ฎ๐ณ
@curesmaindia
Making Spinal Muscular Atrophy treatment and cure accessible and affordable to Indians.
ID:806319759809597440
http://www.curesmaindia.org 07-12-2016 02:09:46
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We are happy to share the latest Community Letter issued by Roche. You can see more here: sma-europe.eu/news/communityโฆ
All together. One goal.
#spinalmuscularatrophy #raredisease #treatment #risdiplam
We r honoured 2 have Mr Vijay Garud, Managing Director, Syniti, n
Mr Srikanth, Director, HR, Syniti join us in commemorating #RareDiseaseDay n supporting #SMArtWarriors
Tku @syniti 4 yr generous donation of medical equipment and motorised wheelchairs 2 SMA patients๐.
Today, on #RareDiseaseDay , CureSMA India stands with all those affected by rare diseases like #SMA . Together, let's raise awareness, promote research, and support one another in our journey towards a cure. Every voice matters in the fight against rare diseases! #BattleAgainstSMA
Heartfelt gratitude to Kerala Chief minister Pinarayi Vijayan , Dept. of Health & FW, Govt. of Kerala Veena George for officially announcing the scheme KARE: Kerala united Against RarE diseases. Kerala Government | เดเตเดฐเดณ เดธเตผเดเตเดเดพเตผ 's free drug program for SMA and free scoliosis surgeries have saved many lives. Thank you๐
๐งฌ #FebRAREuary spotlights a #RareMother โจ
#SpinalMuscularAtrophy is a rare disease found in an estimated 1 in every 6k-10k people. It is a progressive genetic disorder that affects the motor nerve cells in the spinal cord...
Read more at gne-myopathy.org/feb-rare-uary-โฆ
#Motherhood
Congratulations #SMA rtwarrior Dr. Archana Vijayan! Overcoming obstacles, she triumphantly earned her MBBS, passionately pursuing her dream. She aspires to contribute to comfort the patients facing #SMA ! #Inspiration #BattleAgainstSMA
manoramaonline.com/style/she/2024โฆ
Sailesh Kolanu with Venkatesh Daggubati brought out the suffering of #SMA childn #India Hope Telangana CMO PMO India Ministry of Health in reality facilitate the SMA children with the treatment time is running out #Risdiplam #spinraza #zolgensma Cure SMA Foundation of India ๐ฎ๐ณ
#Saindhav Review #Movie #venky75
Super Hit movie ๐ฅ
Thanks for making a movie on Spinal Muscular Atrophy
#SMA #SpinalMuscularAtrophy
curesmaindia.org
You are brilliant Sailesh Kolanu Director #Saindhav Movie
Venkatesh Daggubati ๐ฅ at his best in #Saindhav
It's a gutsy movie
Vโre extremely gr8ful 2 Sailesh Kolanu, Venkat Boyanapalli, Venkatesh Daggubati, Nawazuddin Siddiqui, Arya, Shraddha Srinath 4 highlighting d challenges of #SMA community in d movie #Saindhav ๐. #SMA is a rare genetic disorder wid v.expensive drugs beyond d reach of any #SMA patient/parents.
On this #InternationaldayofPwD our #SMArtWarriors on โฟdemand the society 2 look beyond what they see n accept the warriors as people n not liabilities! Narendra Modi Ministry of Health Ministry of WCD Ministry of Education Ministry of Social Justice & Empowerment, GOI Roche Novartis NovartisGene Biogen Scholar Rock Biohaven
One of the standout aspect of REDRESS 2023 was the narratives from PAGs- from tales of resilience to stories of hope. It underscored the importance of concerted efforts to advance our understanding and treatment of rare genetic dis Indian Prader-Willi Syndrome Association Cure SMA Foundation of India ๐ฎ๐ณ Tata Institute for Genetics and Society, India #Rettsyndrome
To our #SMACommunity that celebrates Diwali, may your festival of light celebrations be fun, safe, and spiritual. #HappyDiwali