Evgenia and her difficult journey. 2
Evgenia and her difficult journey. 2
Active

Evgenia and her difficult journey. 2

The project is carried by
Started: 16.09.2025
Kyiv
Active
Still needed
30170.00 UAH
Funded
21%
Total goal
38500.00 UAH

"Ryzhyk" is the affectionate nickname given to 8-year-old Evgenia by her family. She is a sweet, smiling, and extremely inquisitive girl. When she was born, she was unable to breathe on her own. It later became apparent that she was also unable to eat independently. After an MRI, the doctors announced their diagnosis: congenital nervous system defect, polymicrogyria, lissencephaly, agenesis of the corpus callosum, and cerebellar hypoplasia.

With this list of conditions, Evgenia was transferred to OKHMATDYT, where she spent a month and a half. The doctors did not give any prognosis, but her mother did not give up: she and her daughter followed all the recommendations and believed that they would be able to overcome any difficulties. When she was discharged, the head doctor said words that became a motto for the whole family: "You need to work hard, very hard...". And that is exactly how the family has been living all this time.

Fortunately, their efforts have not been in vain.

"Evgenia has made significant progress: she has started to pick up a spoon and bring it to her mouth on her own, put on and take off T-shirts, sweaters, and socks, feed her doll, point to objects in pictures, distinguish colors, and feel and differentiate textures. Evgenia has begun to feel her body better and even tries to walk on her own, which she really enjoys," her mother shares their small victories.

But there is still a long way to go. To have a chance at new achievements, Evgenia needs further treatment and rehabilitation courses. That is why we are starting to raise funds for another course for our "Ryzhyk". Join us!

Full name: Svystunova Evgenia, 27.12.2016
City: Kyiv
Diagnosis: congenital malformation of the brain: agenesis of the corpus callosum, hypoplasia of the cerebellum, polymicrogyria. Structural epilepsy, focal seizures with spread. Spastic diplegia. Delay in psycholinguistic development
ID: 10537
Supported
28
Середній донат
150 UAH
ТОП-донат
2000 UAH

Your help is needed more than ever. Support the project to add some goodness to this world!

Support

Supported
Charity donation
13.11.2025 16:24
200.00 UAH
Charity donation
11.11.2025 20:55
50.00 UAH
Paul Zavorotnikov
31.10.2025 20:30
30.00 UAH
Charity donation
20.10.2025 09:41
50.00 UAH
Charity donation
11.10.2025 08:34
200.00 UAH
All donors
Similar projects
Matvii remains smiling. 2
Support
Health
Matvii remains smiling. 2
Matvii is mature beyond his years. At 9 years old, the boy measures his own blood sugar levels, monitors…
Sophia wants to live without limits!
Support
Health
Sophia wants to live without limits!
Sofia has Noonan syndrome. It is a congenital genetic disorder. She needs to undergo systematic social a…
Living despite the disease
Support
Health
Living despite the disease
Nikita was diagnosed with diabetes when he was just five years old. Since then, his life has changed dra…
The war left him homeless and without property.
Support
Health
The war left him homeless and without property.
The illness first manifested itself when the young man was thirteen: the doctor, to whom he came with co…
Show All