Request Hon’ble Ministers @nsitharaman Ji @ianuragthakur Ji to kindly approve tax exemptions as the medicines are being shipped on 5th June
Ayaansh, 3 year old child needs all the support you can give asap
Their family, friends & good samaritans have raised ₹16 Cr on their own
Please help Ayaansh get his life saving medicine 🙏🏻 No Amount is too small. On May 27, 2021, he will turn 3 and with that his eligibility to get the life-saving gene therapy with Zolgensma will come to an end. Please help @FightsSma@ImpactGuru
https://t.co/u4T4Geunnx
I urge all to help support 2yrs11months old
Ayaansh. He suffers from a rare genetic disorder SMA Type-1. Help him live life.
Time is of great essence. Pls contribute as per comfort. Thanks🙏 @FightsSma#ZolGenSMA#saveayaanshgupta
https://t.co/eb0herpEeG
Hello Everyone... in all the chaos out there, these little voices are praying to #saveayaanshgupta pls help with whatever little you can and share... 🙏
A beautiful rendition by kids of all ages across the globe appealing to help #saveayaanshgupta, our little son. Very few days are left and our goal of ₹16 Cr. is still far. Pls contribute in the best way you can. You help can mean life to Ayaansh.🙏
https://t.co/3dBx9AL4xl
That's a significant part of the cost but still insignificant if ₹16 Cr. is not reached on time.
I urge everyone to donate an amount as per your capacity.
Donate on the link below. Let’s save Ayaansh. https://t.co/32Wygb4Ujs
99 days of campaigning and we hve raised ₹10 Cr. for Ayaansh's treatment. But we are still ₹6 Cr. short. Requesting twitterati to come frwd and help #saveayaanshgupta . Pls help him get Zolgensma. He's been suffering since birth. Every donation counts.
https://t.co/3dBx9AL4xl
Hello, @Nithin0dha & @zerodha :)
Some more good news, over the last few days, @FightsSma & fam have been able to cross Rs 10 cr.
Its now Rs 6 cr more. Can you & the Zerodha community please pitch in? Stay safe.
@SandeepMall#COVID19 is not the only disease killing. A 3 yr old kid @FightsSma is dying due to spinal muscular atrophy. we need little support from those who can afford small donation for him. 50% funds raised. Plz help before it’s too late 🙏 https://t.co/t0BldSDqGK
The parents of the boy decided to fight to save their child’s life.They have started a Crowd funding campaign to raise this amount.
Pls share this this article so that it reaches to more Donors,
#AyaanshFightsSMA, #DonatetoAyaansh, #SaveAyaansh,#SMA
https://t.co/RjWYWztLNj
Heartily grateful to all who have spoken about #Ayaansh last couple of days. It's a blessing that you have lent your voice for our little boy. We still have a long way to go.
Requesting @SrBachchan@juniorbachchan@earth2angel to help.
#DonatetoAyaansh
https://t.co/rHjq4Y0LPh
Help #Ayaansh Gupta to fight this rare genetic disorder #SMA Type 1. The medicine costs Rs.16 Crores, an impossible amount for any Indian Family. Let’s keep humanity alive.
#SaveAyaanshGupta@FightsSma
Know his story here and donate:
https://t.co/snXq5ed5kD