Urgently

❤️‍🩹Moja córka może siedzieć w fotelu wiecznie❤️‍🩹SMA typ 2🆘 Mięśnie zanikają i powodują ból⚠️POMOCY🆘⚠️❤️‍🩹My daughter may stay in a wheelchair forever❤️‍🩹SMA type 2🆘 Muscles atrophy and cause pain⚠️ HELP🆘⚠️ ❤️‍🩹Моя дочь может остаться на всегда в кресле❤️‍🩹СМА 2-го типа🆘 Мышцы атрофируются и причиняют боль⚠️ ПОМОГИТЕ🆘⚠️


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Новости Кати🗞️ мышцы слабнут❤️‍🩹Nowość Katyi❣️ mięśnie osłabnąKatyas news❤️muscles will weaken‼️

Vinogradova Ekaterina Vinogradova Ekaterina Виноградова Екатерина , 7 lat7 years old 7 лет

Диагноз

❤️‍🩹Moja córka może siedzieć w fotelu wiecznie❤️‍🩹SMA typ 2🆘 Mięśnie zanikają i powodują ból⚠️POMOCY🆘⚠️❤️‍🩹My daughter may stay in a wheelchair forever❤️‍🩹SMA type 2🆘 Muscles atrophy and cause pain⚠️ HELP🆘⚠️ ❤️‍🩹Моя дочь может остаться на всегда в кресле❤️‍🩹СМА 2-го типа🆘 Мышцы атрофируются и причиняют боль⚠️ ПОМОГИТЕ🆘⚠️.

Цель сбора

Drogi lekExpensive drugДорогостоящий препарат

Собрано:
285 $
Сумма сбора:
15800 $

History

🆘⚠️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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