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  • 11-month-old Vedika To Be Injected with Zolgensma, The World’s Most Expensive Drug

    By NE Reporter on May 30, 2021

    THIRUVANANTHAPURAM:
    Vedika Shinde, a 11-month-old baby from Pune, was diagnosed with SMA Type-1, a rare genetic disorder that can take a child’s life before the age of 2. In Vedika’s case, as the diagnosis was done at an early stage, the doctors were optimistic about her recovery.

    A gene replacement therapy (Zolgensma), which would cost INR Rs 16 Crores (USD 2.1mn), had to be imported urgently to save the baby. Vedika’s parents narrated their story on the fundraising platform Milaap and requested help from online donors across the world. The fundraiser which was set up in the month of March received humongous support in the days that followed. In less than three months, a sum of INR 14.3 Cr was raised from the generosity of donors who supported the campaign on Milaap.

    The parents were successful in getting a waiver from the government authorities on taxes and import duties. The doctors have already raised a request to a renowned US pharmaceutical company for Zolgensma. Vedika, who must get the treatment before her first birthday, in June, is now undergoing a few mandatory tests to get the drug custom made for her. The drug is expected to reach by 2nd july and the treatment is expected to happen between the 7th and the 10th of July.

    The fundraising campaign on Milaap had earned great attention from the media in the initial phase itself. A sum close to INR 1 Crore was raised in the first week. Nearly 50 support campaigns were started for the same cause on Milaap. Numerous social media influencers like Barkha Singh, Master Chef Shipra Khanna and parenting influencers like AnupriyaKapur and many others helped in amplifying the cause.

    Renowned Bollywood actor John Abraham came forward to extend his support by appealing to his fans on his social media handles. A video made by Milaap in which Vedika’s mother Sneha makes an appeal was watched by over 3 lakh people on Facebook. Deeply moved by the overwhelming response, parents have recently posted another video on Milaap’s fundraiser page thanking all the donors for helping them to give Vedika a chance at a better quality of life.

    Having taken up the challenging task of raising such a huge amount in such a short span, South Asia’s largest crowdfunding platform, Milaap had seen positive signs of support right from the beginning.

    Commenting on the success of this campaign, Anoj Viswanathan, President and Co-founder of Milaap says “We had a challenging goal in front of us and very limited time to reach the same. Milaap’s team was absolutely determined to do everything in their capacity to ensure the required funds were raised before Vedika’s first birthday. Amidst a flurry of COVID-19 fundraisers, which were also in need of urgent funds, Milaap ensured that donors of Vedika’s fundraiser were updated time to time about the treatment progress and the challenges faced by the family due to shortage of funds.”

    Expressing his faith in Vedika’s recovery he added, “As Vedika is undergoing the mandatory tests before the treatment and the injection is expected to reach India in the coming week, Milaap wishes her a speedy recovery”. The campaign’s success sends a message of hope that funds can be sourced for such rare and cost intensive treatment procedures. Milaap in the last one year has raised more than INR 250 Crore for medical causes including emergency medical care. INR 31 Crore was raised exclusively to support intensive care requirements. The platform’s donor base spread across the globe gives the deserving visibility for an urgent need.

    NE Reporter

    crowdfunding platformgene replacement therapygenetic disorderJohn AbrahamMilaapSMA Type-1Vedika ShineZolgensma

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