Little Eva wants to walk

The Lytvyn family has two children, and unfortunately, two of them have disabilities. The eldest son has a chest deformity, and the youngest daughter, Eva, has central nervous system damage, spastic paraplegia, and dysarthria. This aid project is about Eva and for her.

The girl was born prematurely at 28 weeks, and the baby was nursed for a month and a half in the intensive care unit and the same amount of time in the premature birth unit. After Eva turned a year old, she was diagnosed with lower spastic paraparesis with persistent severe motor disorders. "We are making every effort to put our daughter on her feet, as at the age of 3 she cannot move her legs independently. Despite this, she is a very active and positive girl," says Eva's mother.

Systematic rehabilitation is recommended for the girl, which significantly improves her condition: her appetite and sleep improve, her vocabulary increases, and most importantly, after the last course of treatment, Eva began to stand independently with the help of orthoses and take her first steps! Of course, there is still a lot of work to be done and the necessary treatment to be completed, but there is progress, and this is very important.

In this family, the father tries to provide for all the members on his own, but the ongoing treatment of children requires considerable funds, so we ask you to support our project so that Eva can get into a new rehabilitation course. Let's help this wonderful girl walk on her own!