AyanshMadan_fight_SMA

*FB* https://bit.ly/3zVDQ7Q
*twitter* https://bit.ly/2X9Vlmc
*Insta* https://bit.ly/3C2s1xt
*youtuube* https://bit.ly/3neJHBM
*Vandana Madaan Whatsapp* https://bit.ly/3z1nLMu

Help!!

Please help us! This fundraiser can save our son's life

Ayansh needs your help and blessings. Please contribute as much as possible and share our request with your friends and family🙏🏻

Please click to DONATE :

https://linktr.ee/AyanshMadan

You can make your donations at

Gpay/ Phone Pay/ Paytm: 9717741714

Upi Id: Vandumadan@okicici

For Bank Transfers:
Account Name: *Ayansh Madaan*
Account No.: *15280100050922*
IFSC Code: *FDRL0001528*
Branch Name: *Federal Bank DLF, Gurgaon*

Help us!

https://youtu.be/5UYZzHAKHEg

16 करोड़ के इंजेक्शन के लिए बच्चे की जान लगी दाव पर।।

Media coverage.


Parveen Grover Naveen Goyal Deepak Mangla Gurgaon News

आयाशं 14 months का हो गया है ,लेकिन अभी वह अपने बल पर बैठ नही सकता | भगवान ने उसे दिमाग दिया है, समझदार भी बनाया है , आवाज भी दी है, लेकिन एक जीन नही
दिया | यह जीन शरीर मे खास Protin बनाता है ,जिससे Body की सारी Muscles चलती है | इस जीन के बिना आयाशं का जीवन अधूरा है | Zolgensma injection ही आयाशं की सारी Problem का हल है, लेकिन injection की कीमत 16 करोड़ रुपये है, जो कि आप सबकी मदद के बिना जुटा पाना नामुकिन है|
अगर आप सभी का सहयोग मिले तो 16 करोड़ भी जुड़ जाएगे और मेरे बेटे को नया जीवन मिल जाएगा | फिर आयाशं भी खेलेगा,कूदेगा |आप का छोटा सा अंशदान अयांश को दे सकता हे, नया जीवन I 🙏🙏🙏🙏

*Read More:* http://impactguru.com/s/IaiPGj

*Donate Here:* http://impactguru.com/s/57jAvd

*Paytm Karo (Android Users Only):* http://impactguru.com/s/paytm-ayansh-madan

Support Ayansh Madan raise funds to fight SMA - Impact Guru Parveen Madaan wants to raise funds for his baby Ayansh Mada to fight SMA. Your donation can guide them to reach their fund goals. Please help.

AyanshMadan_Fight_SMA

http://impactguru.com/s/IaiPGj

Support Ayansh Madan raise funds to fight SMA - Impact Guru Parveen Madaan wants to raise funds for his baby Ayansh Mada to fight SMA. Your donation can guide them to reach their fund goals. Please help.

http://impactguru.com/s/IaiPGj

Ayansh’s life is incomplete due to gene deficiency, Rs 16 crore injection expected

Timesofindia India Today Hindustan Times

http://impactguru.com/s/IaiPGj

Please support, love n contribute towards SMA disease medication
Varun Pruthi Sonu Sood

“We have no words to describe the gratitude we feel towards your compassion & commitment towards our little one,” says Teera's father, Mihir Kamat.

A lockdown baby born in August 2020, Teera was 2 months of age when she was diagnosed with Spinal Muscular Atrophy Type 1 -- a rare genetic disease that cause weakness and wasting in the voluntary muscles of infants and children.

While there is no cure for SMA, there is Zolgensma, a one-time gene replacement therapy, which in her current state could be a potential cure.

So Teera’s parents set up a fundraiser for a whopping 16 crore to pay for her Zolgensma treatment. The good news? They raised the money and then some.

Little Teera received donations from 1 lakh people for the life-saving treatment. Social media at its best!