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Thanks to your support, a vital genetic test has been conducted for Eleazar.

Pomosch

Charitable foundation · St. Petersburg

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of RUB 105,504

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Dear friends, thanks to you, this crucial test has been performed for 14-year-old Eleazar. This analysis was the key to treating a rare neurodegenerative disease.

The results of the study are already being reviewed by doctors and have helped them adjust his therapy. Now, Eleazar and his family can focus on fighting the disease, and thanks to you, this boy has a chance at a healthy future!

A long road lies ahead for this smiling and kind teenager, who dreams of helping other children. But the first and most difficult step — diagnosis and the start of proper treatment — has been taken, thanks to you!

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About the campaign

Eleazar has several diseases. He needs to undergo examination to get the right treatment!

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.