Many thanks @PPHF_Asia. Let’s prioritise rare disease 2gether. Join us 4 d North Region Rare Diseases consultation, an initiative by Govt. of Chandigarh, Punjab & PPHF 2 b held on Jan 22, 2021 frm 10:00 to 1300hrs. @MoHFW_INDIA@PMOIndia#BattleAgainstSMA https://t.co/nb0ul6cCp8
We @curesmaindia r extremely grateful to @ThePksinha@SPJIMR@NovartisIndia for d exceptional learning opportunity through #Saksham The learning Continues empowering the patients, caregivers, health care professionals to make the best use of resources in these unprecedented times
Thanks Amruta Durve for the insightful article on #Teera’s struggle. As parent it’s absolutely heartbreaking for us @curesmaindia to see our children slowly wasting away in front of our eyes despite a life saving treatment available but not accessible @PMOIndia@narendramodi
@KTRTRS Sir, Happy Republic Day from CureSma India,we r keeping a big hope on you,one day you will get the #SpinalMuscularAtrophy medicine #Risdiplam#ZolgenSma#Spinraza to SMA kids who r leading painful life & dying as medicine is getting delayed,pls show mercy & save #SMA kids
On this #Christmas Day, we wish the world to heal soon!With no medicine available yet in India, SMA families still live in the constant #fearforlife.
Our children wish for SMAmedicine -#Risdiplam, #Spinraza, #Zolgensma for which we need your financial help. Will you #BeOurSanta?
Vaccines and returning to normalcy isn't promising when I have to keep my muscles functioning or be bedridden and kids with my disease die before they say their first word. We finally have treatment options but affording it is tough. @curesmaindia needs you to spread the word.