Eva has type 1 spinal muscular atrophy. Previously, children with this diagnosis did not live to be 2 years old - the body gradually became weaker, the smooth muscles atrophied, and the child stopped breathing. But the state allocated 150 million rubles for the most expensive medicine in the world for little Eva, and her disease no longer progressed. Now she will live, and she has every chance to regain muscle function - to learn to sit, walk, and run.
But this requires rehabilitation. Eva is advised to start getting used to the upright position now, so that one day she will be able to take her first step and walk. She needs a good vertical positioner, which is not only suitable for such a baby, but also grows with her.
Unfortunately, the region where Eva lives does not buy such models. And parents cannot cope with the purchase. Let's help Eva to forget about her disease, and just live like all children!
Спасибо ❤️ занятия спасут Еву от тяжёлых осложнений. Вы лучшие!
Мира, добра, любви и справедливости 🕊️🕊️🕊️желаю всем искренне помогающим💕💕💕
Всё будет хорошо 🙏🙏🙏
+ для Евушки! Давайте, друзья, вместе поможем!