Help Vihaan fight SMA

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  • April 15, 2022 at 11:32 pm #5315
    michaelkhanna
    Keymaster

    Hi Friends. I request to please donot ignore this post. This post is for my 16 month nephew Vihaan who suffers from rare genetic disorder Spinal Muscular Atrophy. His muscles are losing strength by each passing day. He currently has no thigh movement & cannot sit, walk or crawl by himself. Only medication available is Zolgensma but it costs $ 2.1 Million in India. In US, some of it is covered by insurance. To save Vihaan we are looking for various avenues to get him the treatment needed, one of them was to travel to united states. Does anyone have idea around how to go about getting medical visa, what is processing wait time?

    Please follow Vihaan fights SMA for more details on his medical condition.

    https://linktr.ee/helpvihaan

    Thank you!

    • This topic was modified 7 months, 3 weeks ago by michaelkhanna.
    April 16, 2022 at 12:12 am #5317
    Anonymous
    Inactive

    (Awaiting moderation)

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