Hello Everyone,

JIYENGE INDIA TEAM is helping to raise funds for BABY DAYANA SHANTHI who is suffering from SMA TYPE - 2.

The parents of baby are trying very hard for the injection with the support of government. The funds which we are raising now this will be used for baby medications and hospitality purpose for the present situation.

Unfortunately Dayana Shanthi has Diagnosed with this life threatening genetical disease and if Untreated Spinal Muscular Atrophy Type2 may take away Dayana shanthi life.She has very less time to Survive.

Zolgensma Gene therapy is the Only Option to Save Dayana's life and the Zolgensma drug need to Import from United States.

Their parents have taken the Zolgensma drug Import License from CENTRAL DRUG STANDARD CONTROL ORGANISATION,MINISTRY OF HEALTH,GOVERNMENT OF INDIA, but due to insufficient funds,they couldn't able to afford the Treatment.

Your Contribution is the Only hope to save Dayana Life and to give her a chance to Live a normal life.

Please contribute as much as you can and share this information to all your friends and family Members.

The funds which we have received through jiyenge upi/Gpay or Phonepe (9701849704) will be added as JIYENGE UPI in the bottom of supporters list. The amount will be added at end of the day/twice a day. 

Treatment Options: Zolgensma Gene Therapy is a potential cure for SMA for children below two years of age and it has to be imported from the USA. Baby Dayana needs it as soon as possible to save her life. Zolgensma Gene Therapy is a one-time gene replacement therapy, and it needs to be imported. Called the world's costliest drug, it costs 16 crore rupees and is more expensive than any family can afford alone.

Any contribution will be of immense help. Please share, support & contribute as much as possible. Nothing is small or big. Every penny counts. Thank you all in advance.

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