Cure SMA Foundation of India ๐Ÿ‡ฎ๐Ÿ‡ณ(@curesmaindia) 's Twitter Profileg
Cure SMA Foundation of India ๐Ÿ‡ฎ๐Ÿ‡ณ

@curesmaindia

Making Spinal Muscular Atrophy treatment and cure accessible and affordable to Indians.

ID:806319759809597440

linkhttp://www.curesmaindia.org calendar_today07-12-2016 02:09:46

4,3K Tweets

2,1K Followers

618 Following

SMA-Europe(@SMAEurope) 's Twitter Profile Photo

We are happy to share the latest Community Letter issued by Roche. You can see more here: sma-europe.eu/news/communityโ€ฆ

All together. One goal.

We are happy to share the latest Community Letter issued by Roche. You can see more here: sma-europe.eu/news/communityโ€ฆ All together. One goal. #spinalmuscularatrophy #raredisease #treatment #risdiplam
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Cure SMA Foundation of India ๐Ÿ‡ฎ๐Ÿ‡ณ(@curesmaindia) 's Twitter Profile Photo

We r honoured 2 have Mr Vijay Garud, Managing Director, Syniti, n
Mr Srikanth, Director, HR, Syniti join us in commemorating n supporting
Tku @syniti 4 yr generous donation of medical equipment and motorised wheelchairs 2 SMA patients๐Ÿ™.

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 patients๐Ÿ™.
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Cure SMA Foundation of India ๐Ÿ‡ฎ๐Ÿ‡ณ(@curesmaindia) 's Twitter Profile Photo

Today, on , CureSMA India stands with all those affected by rare diseases like . 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!

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
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Scholar Rock(@ScholarRock) 's Twitter Profile Photo

Weโ€™re excited to announce the addition of Katie Peng to our Board of Directors.

Katie brings deep commercial expertise in neurology and rare diseases, including SMA from her experience launching Evrysdi while at Genentech.

Learn more: bit.ly/3SJf9WO

Weโ€™re excited to announce the addition of Katie Peng to our Board of Directors. Katie brings deep commercial expertise in neurology and rare diseases, including SMA from her experience launching Evrysdi while at Genentech. Learn more: bit.ly/3SJf9WO
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World Without GNE Myopathy (WWGM)(@wwgnem) 's Twitter Profile Photo

๐Ÿงฌ spotlights a โœจ

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-โ€ฆ

๐Ÿงฌ #FebRAREuary spotlights a #RareMother โœจ #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-โ€ฆ #Motherhood
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Scholar Rock(@ScholarRock) 's Twitter Profile Photo

We are proud to see 12-month data from our Phase 2 TOPAZ study in a leading publication. These data led to the design of our Phase 3 SAPPHIRE trial, which completed enrollment last September.

Read more: bit.ly/3wh4OKf

We are proud to see 12-month data from our Phase 2 TOPAZ study in a leading publication. These data led to the design of our Phase 3 SAPPHIRE trial, which completed enrollment last September. Read more: bit.ly/3wh4OKf
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Cure SMA Foundation of India ๐Ÿ‡ฎ๐Ÿ‡ณ(@curesmaindia) 's Twitter Profile Photo

Congratulations rtwarrior Dr. Archana Vijayan! Overcoming obstacles, she triumphantly earned her MBBS, passionately pursuing her dream. She aspires to contribute to comfort the patients facing !

manoramaonline.com/style/she/2024โ€ฆ

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Scholar Rock(@ScholarRock) 's Twitter Profile Photo

Weโ€™re excited to announce that Scholar Rock will be presenting at on Tuesday, January 9th. For more information and a link to the live webcast, please visit our website: bit.ly/3RPyMgP

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Cure SMA(@CureSMA) 's Twitter Profile Photo

Our partners at Genentech recently provided an SMA Community Letter regarding Evrysdiยฎ (risdiplam) and their clinical development program.

You can read the full letter here: curesma.org/genentech-commโ€ฆ

Our partners at @genentech recently provided an SMA Community Letter regarding Evrysdiยฎ (risdiplam) and their clinical development program. You can read the full letter here: curesma.org/genentech-commโ€ฆ
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Runa Hamid(@RunaHamid) 's Twitter Profile Photo

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 ๐Ÿ‡ฎ๐Ÿ‡ณ Tata Institute for Genetics and Society, India

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 @IPWSA_ @curesmaindia @TIGS_India #Rettsyndrome
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Cure SMA Foundation of India ๐Ÿ‡ฎ๐Ÿ‡ณ(@curesmaindia) 's Twitter Profile Photo

CureSMAIndia wishes a happy, healthy and prosperous Diwali to everyone ๐ŸŽ‰๐ŸŽŠ๐ŸŽ‰๐Ÿ’๐Ÿ’โญ๐ŸŒŸ๐Ÿช”๐Ÿช”๐Ÿช”๐Ÿช”๐Ÿช”๐Ÿช…๐ŸŒธ๐Ÿชท๐ŸŒบ๐ŸŒผ๐Ÿ’ฎ๐Ÿ™

CureSMAIndia wishes a happy, healthy and prosperous Diwali to everyone ๐ŸŽ‰๐ŸŽŠ๐ŸŽ‰๐Ÿ’๐Ÿ’โญ๐ŸŒŸ๐Ÿช”๐Ÿช”๐Ÿช”๐Ÿช”๐Ÿช”๐Ÿช…๐ŸŒธ๐Ÿชท๐ŸŒบ๐ŸŒผ๐Ÿ’ฎ๐Ÿ™
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