shubham sharma

Chai and love.

[shubham sharma @Sh57127]

@CMMadhyaPradesh @CollectorGwalior @GwaliorComm MP ki beti ko bachana hai. Neelakshi Bhargava (1 yr, SMA Type 2) ko Zolgensma chahiye. Kripya CM Relief Fund se madad aur AIIMS Bhopal me referral provide kare. Verified fundraiser: https://t.co/qTthR9RP60

[shubham sharma @Sh57127]

@CMMadhyaPradesh @DrMohanYadav51 @healthminmp Respected Sir, MP ki 1 saal ki beti Neelakshi Bhargava SMA Type 2 se lad rahi hai. Usko 15Cr ki therapy chahiye. Pls help from CM Relief Fund & refer to AIIMS Bhopal for rare disease support 🙏

[shubham sharma @Sh57127]

@PMOIndia @MoHFW_INDIA Sir, 1-yr-old Neelakshi Bhargava from MP has SMA Type 2 & needs Rs 15Cr Zolgensma therapy. Family is middle class. Registered on rare disease portal. Pls help under PMNRF & grant customs duty exemption for life-saving drug 🙏
https://t.co/qTthR9RP60

[shubham sharma @Sh57127]

@Cockroachisback @AshutoshRanka @abhijeet_dipke @SauravDassss
Need genZ superpower here. 1yr old baby vs SMA Type 2. 15Cr injection can save her. Your 1 quote RT can reach a donor. Can we help her go viral for life?

[shubham sharma @Sh57127]

This is 1-yr-old Neelakshi. She has SMA Type 2, a rare disease where muscles slowly stop working.She needs a Rs 15 Cr Zolgensma injection to LIVE.Pls read her story 🧵👇https://t.co/qTthR9RP60
@ril_foundation

[shubham sharma @Sh57127]

@Cockroachisback @AshutoshRanka @abhijeet_dipke @SauravDassss
CJP fam, need your reach here. 1-yr-old Neelakshi is fighting SMA Type 2. Needs 15Cr Zolgensma to survive. If genZ can make songs viral, we can make this fundraiser viral too. Pls amplify 🙏

[shubham sharma @Sh57127]

This is 1-yr-old Neelakshi. She has SMA Type 2, a rare disease where muscles slowly stop working.She needs a Rs 15 Cr Zolgensma injection to LIVE.Pls read her story 🧵👇https://t.co/qTthR9RP60
@ril_foundation

[shubham sharma @Sh57127]

@Cockroachisback @AshutoshRanka @abhijeet_dipke @SauravDassss
genZ, we meme every day, can we save a 1yr old today? Baby Neelakshi has SMA Type 2 & needs Rs 15 Cr injection to live. Even 1 RT = huge help. 🙏

[shubham sharma @Sh57127]

This is 1-yr-old Neelakshi. She has SMA Type 2, a rare disease where muscles slowly stop working.She needs a Rs 15 Cr Zolgensma injection to LIVE.Pls read her story 🧵👇https://t.co/qTthR9RP60
@ril_foundation

[shubham sharma @Sh57127]

@ril_foundation @ImpactGuru "I dream of seeing Neelakshi walk into a classroom" - her father.Let's not let that dream die.Pls donate, share, pray.🙏@RFHospital @MoHFW_INDIA @PMOIndia
#SaveNeelakshiBhargava

[shubham sharma @Sh57127]

This is 1-yr-old Neelakshi. She has SMA Type 2, a rare disease where muscles slowly stop working.She needs a Rs 15 Cr Zolgensma injection to LIVE.Pls read her story 🧵👇https://t.co/qTthR9RP60
@ril_foundation

[shubham sharma @Sh57127]

@ril_foundation There is a cure: Zolgensma, a one-time gene therapy. It's the world's most expensive drug.Cost: Rs 15 CRORE.Her family can't afford it. The campaign is verified on @ImpactGuru.Link: https://t.co/qTthR9RP60

[shubham sharma @Sh57127]

@ril_foundation @ImpactGuru How YOU can help:Donate - even Rs 100 helps (80G exempt)Share this thread & tag 2 friendsIf you are in CSR/Media/NGO - connect family to a donorLink: https://t.co/qTthR9RP60

[shubham sharma @Sh57127]

@ril_foundation @ImpactGuru Why URGENT?Zolgensma works best before age 2. Neelakshi is 1.Every week = more muscle loss. Doctors say treat NOW.We have days, not months.#HelpNeelakshiBhargava #SMAWarrior

[shubham sharma @Sh57127]

@ril_foundation @ImpactGuru People who saved SMA babies before, pls amplify:@SonuSood @SoodFoundation
@AnupamMittal @nikhilkamath @vivekoberoiYour 1 RT has saved lives before. Pls help Neelakshi reach a donor.

[shubham sharma @Sh57127]

@ril_foundation @ImpactGuru @ril_foundation @NitaAmbani Ma'am, you have saved so many children through your health initiatives.Neelakshi's case is verified. Please help her get this life-saving therapy. One support can give her a lifetime.#SaveNeelakshi

[shubham sharma @Sh57127]

@ril_foundation Respected @NitaAmbani @ril_foundation Ma'am, a little girl Neelakshi (1 yr) is fighting a rare genetic disorder SMA. Her family cannot afford the ₹15 Cr gene therapy. Your foundation has saved so many lives. Please help Neelakshi get her childhood back 🙏
https://t.co/qTthR9RP60

[shubham sharma @Sh57127]

@ril_foundation 🙏 1-year-old Neelakshi Bhargava is fighting SMA Type 2, a rare disease where her muscles are weakening every day. She needs a ₹15 Cr life-saving Zolgensma gene therapy. Please help save her life @NitaAmbani_Foundation
Donate/Share: https://t.co/qTthR9RP60

[shubham sharma @Sh57127]

@ril_foundation @ril_foundation Namaste 🙏 1 saal ki Neelakshi SMA Type 2 jaisi gambhir bimari se lad rahi hai. Maa-baap ka sapna hai ki beti chale, school jaye. Par 15 Crore ki Zolgensma dawai ke bina ye sapna toot jayega. Aap madad kar dijiye 🙏
https://t.co/qTthR9RP60
#HelpNeelakshi

[shubham sharma @Sh57127]

@ril_foundation Every share counts! 🥺
Baby Neelakshi, 1 yr old, SMA Type 2 fighter needs ₹15 Crore Zolgensma injection to survive.
@ril_foundation can you please help this angel? 🙏
👉 https://t.co/qTthR9RP60
Please RT #SaveNeelakshiBhargava

[shubham sharma @Sh57127]

@ril_foundation SOS! A 1-year-old baby girl from India needs urgent gene therapy to LIVE.
Neelakshi has SMA Type 2. Without Zolgensma (₹15Cr), she may never walk.
@ril_foundation @RFHospital Please look into her case & support her treatment 🙏
Link: https://t.co/qTthR9RP60

[shubham sharma @Sh57127]

@heydigit I was waiting on workshop for 2 hours but no one on your escalation team picked call or contacted back this is the level of service .

[shubham sharma @Sh57127]

Is @heydigit’s "quick claim settlement" just a marketing myth? 🚨

I’ve been running in circles for weeks while Go Digit closed my legitimate claim (#202601099900) citing "No Response." The reality? Their network workshop refused intake 3 TIMES due to overload! 🧵👇