Baby Rehansh

Hello, help me Battle a Rare & Deadly Disease. I require your help to Live a Healthy & Happy Life!

[SunilKapoor 4 Free #Hospital,Treatment @sunilkapoor8]

@curesmaindia @kutchinadotcom @NamitBajoria06 @SMA_mom @GautamGambhir @drharshvardhan @anandmahindra @DrJoyeeta @ua_shirin @KapilChopra72 @PMOIndia @Tejasvi_Surya @IGeetaSharma @Karan_Gilhotra @GovindAgarwal_ @SonuSood Spoke to @GovindAgarwal @Sonusood, requested to help @BRehansh who is raising 16cr for
#SpinalMuscularAtrophy #BattleAgainstSMA
treatment. They said working on it, they hv five patients request with them.

[kanika Arora @kanikaA91783354]

If we wish to be a developed nation, we need implementation plans in all sectors like developed nations.

https://t.co/qBPJd2nkeJ

@PMOIndia @ICMRDELHI @CDSCO_INDIA_INF @drvgsomani @drharshvardhan
@KapilChopra72 @BRehansh

[ANI @ANI]

Children with this disease don't survive beyond 2 yrs. He's fine now but is going to get weaker & won't be able to sit, swallow or breathe. There's only 1 treatment where he can be given a missing genetic code via virus. It's a one-shot cure & most expensive drug: Dr Anne Mathew

[Baby Rehansh @BRehansh]

@kundan19821 @ANI https://t.co/KhOs9oRqxt

[Baby Rehansh @BRehansh]

@nitinchandra09 @ANI https://t.co/KhOs9oRqxt

[Baby Rehansh @BRehansh]

@nitinchandra09 @ANI Thank you for supporting us. Link to the crowdfunding is below:
World's Costliest Drug Zolgensma Is Rehansh's Only Hope!
https://t.co/SCMUZzOBP8

[Baby Rehansh @BRehansh]

Field specialist Dr Ann Agnes explaining SMA in simple words.@ANI
‘one spelling mistake’ must not take our child away. ‘Each one save one’.
Contribute as little as you can and it will help us filling the big pot.

https://t.co/jwzt8F4YCn

[Madhu M @MadhunaikBunty]

@SuchitraMukher2 @BRehansh @IamNaveenKapoor Litrally my eyes were full when doctor explaining about the fight of the little one. I wish India helps this family to save @BRehash

[Suchitra 🇮🇳 @JurnoSuchitra]

Delhi couple resorts to crowdfunding for treatment of their infant suffering from rare genetic disorder - The Daily Guardian
@SuchitraMukher2&
@MadhunaikBunty Report-ANI
@BRehansh
@IamNaveenKapoor https://t.co/iIGJSEoOzr

[Baby Rehansh @BRehansh]

@ksinghania86 @ANI @SwatiLokhandwa1 @GautamGambhir https://t.co/KhOs9oRqxt

[Baby Rehansh @BRehansh]

@akshatkumar87 @ANI https://t.co/KhOs9oRqxt

[Baby Rehansh @BRehansh]

@im_pjain @ANI @smitaprakash https://t.co/KhOs9oRqxt

[Baby Rehansh @BRehansh]

@ajaymishravlog https://t.co/KhOs9ozPFV

[Baby Rehansh @BRehansh]

@Balasub80706454 @ANI https://t.co/KhOs9oRqxt

[Baby Rehansh @BRehansh]

@Nc07813715 @ANI https://t.co/KhOs9oRqxt

[Baby Rehansh @BRehansh]

@Rajaadh22482433 @ANI @SonuSood @anandmahindra @narendramodi @Dev_Fadnavis https://t.co/KhOs9oRqxt

[Baby Rehansh @BRehansh]

@Chandan01648871 @ANI Below is the link for crowdfunding, if u personally wish to connect us please drop us a personal message.

https://t.co/KhOs9oRqxt

[Baby Rehansh @BRehansh]

Today we have crossed a mark of over
known and unknown 1000 donors who are fighting this battle along with us to save Rehansh.
Forever grateful & filled with gratitude

https://t.co/jwzt8ENnKP

#save_rehansh_from_sma

[ANI @ANI]

Delhi: Parents of 10-month-old Rehansh Suri seek crowdfunding support to avail treatment for him.

"He's suffering from Spinal Muscular Atrophy Type I, a rare genetic disease. He can only be treated with a US-based Gene therapy worth Rs 16 cr. We can't afford it," says his mother

[RJ Teena @MyrjTeena]

Done my bit....humble request to everyone on my fleet to help save this child @BRehansh 💟 who's suffering a rare genetic disease Spinal Muscular Atrophy Type I
Crowd Funding Link is in the appended tweet

My prayers for his good health and recovery 🙏🙏🙏