Save_Vitusha by providing Elevidys-new drug for DMD
Donation protected
Hi, my name is Yana Leonova, and I am fundraising for a little boy, Vitusha (Victor), who suffers from an incurable (till 2023 decease) Duchenne muscular dystrophy .
'My name is Vitya. I am 8 years old. In 2022, my life was divided into BEFORE and AFTER. I was given a terminal diagnosis of Duchenne muscular dystrophy: muscles are replaced by fatty tissue; in 1-2 years, I will stop walking and sit in a wheelchair. And then it gets worse...
In 2023, I got a chance - a drug called Elevidys, which could save my life. This drug is available in the USA and UAE. In July 2024, we were in Dubai and having passed the necessary tests, the doctor confirmed that I was still eligible to receive the drug. And while I’m walking on my own feet, I need this drug vitally.
The price of my life is $2,901,907. HELP! On June 21, 2024, Dad died without ever hearing the words “COLLECTION CLOSED.”
We ask everyone for help and participation in the collection. Any amount, repost, likes. Please don’t pass by.
Details for helping Vitya:
SIEPOMAGA Foundation
TRUST WALLET USDT
TCMfX55KHEVC41dnbsphsxcCWFmQ5iSm76
PAY PAL
Michael-21@msn.com
BOOSTY
Tinkoff
2200 7009 0614 3051
#dubai #medcare #duchenne #duchennemusculardystrophy #duchenneheroes
Organizer
yana leonova
Organizer
England