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Vinogradova EkaterinaVinogradova EkaterinaВиноградова Екатерина, 7 years old7 lat7 лет

Diagnosis

Spiral muscular atrophy type 2 SMASpiralny zanik mięśni typu 2 SMAСпиральная мышечная атрофия 2 типа СМА.

Purpose of fundraising

Expensive drugDrogi lekДорогостоящий препарат

Story

🆘⚠️I am the mother of a little girl, Ekaterina Vinogradova, from Kobrin. My daughter has SMA (Spinal Muscular Atrophy Type 2), and the disease causes atrophy of the muscles of the whole body, ⚠️ swallowing and breathing. Katyusha will be 7 years old on September 1. Katyusha has already lost the ability to walk. Katyusha was diagnosed in December 2019. An expensive drug, has been developed for this, which costs more than millions of dollars 💲 US dollars. The drug is administered up to 21 kg. Katyusha already weighs 17 kg. We ask all caring people to help Katyusha collect money for an injection. We will be grateful in advance for your help. Together we can save Katyusha's life.❗

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