I want to help this child see the full life!

Artem Martynov ( Артем Мартынов) https://instagram.com/artem_martynov_help?igshid=hy5ktwymt1pj was born on June 28, 2018. He grew up like a normal baby until at the age of 9 months he suddenly began to weaken. In May 2019, a genetic analysis confirmed the diagnosis of Spinal Muscular Atrophy Type 1-2 (SMA).

This little child is suffering disease, which can be cured with a medical shot worth $2mln. This shot will save his life for ever and would let him live the normal life. The problem is that he has to get this shot by the time he turns 2years old, which is in 28 days! At the moment his muscles aren’t able to move the way regular children do... and one shot can change it for ever...

This is a rare genetic disease leading to painful and complete paralysis of the child. First, the feet of such children stop moving, then the hands, the head stops holding, and the body gradually ceases to obey. This is a slow death, terrible for a small person who does not understand what is happening to him.

Thanks to https://www.zolgensma.com/, the disease can be completely stopped by making just one injection before the child is 2 years old. This is the only such effective drug in the world for the treatment of SMA, and now it is the most expensive drug in the price of $ 2.125 M. The one injection will stop the disease forever, but it is necessary to make as soon as possible to stop irreversible processes in the body.

Any help matters, we ask you to help as much as possible.

Details for help:

PayPal: ekaterinamartynovaa@mail.ru

PayPal: art_martynov@mail.ru

Our fond: veravdetstvo.ru (tagged to Artyom Martynov)

Our web site: ARTEM2020.ru

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