Eleasar is 14 years old. Up until one year old, he developed like a normal baby, but after one year, his mother began to notice that her son had difficulty sitting and standing up, and that movements caused him pain. Doctors diagnosed him with cerebral palsy, and recently it turned out that Eleazar also has a rare neurodegenerative disease - ataxic syndrome.
Eleasar is a smiling and kind boy, he loves to learn new things, and dreams of helping children like him.
Eleasar and his mother are currently in St. Petersburg, where he underwent surgery on his knee joints to reduce spasticity and help with verticalization. Doctors believe that he will at least be able to stand and feel his body, and then - go to new heights.
The next step is an expensive genetic study, without which precise treatment is impossible. The family does not have such funds. Any support is a chance to give Eleasar more strength and opportunities for the life he dreams of.
