My non-childish dream
My non-childish dream
Completed

My non-childish dream

The project is carried by
Started: 02.12.2021
Sumy region
Completed
Totally raised
30000.0 UAH
Funded
100%
Total goal
30000.00 UAH
12.04.2022 13:21
The project is implemented
dobro.ua dobro.ua ICF "Ukrainian Philanthropic Marketplace"
Dear donors! We are pleased to announce that this project has been successfully implemented. A detailed report can be found in the "Reports and documents" section. Thanks to everyone who supports us!
21.02.2022 10:37
Моя недитяча мрія
Виктория Чередниченко CO CF "KYIAN"
Моя недитяча мрія
Завдяки спонсорам Фонду Киян на початку лютого ми разом з моєю донечкою Алісою (3,5 роки) пройшли курс реабілітації у Центрі Стимуляції мозку м. Київ. В цьому центрі ми були вперше. Мене як маму вразив широкий спек…
02.12.2021 18:10
Start of the project.
Supported
62
Середній донат
140 UAH
ТОП-донат
10000 UAH
Supported
Charity donation
10.12.2021 18:58
2954.00 UAH
Charity donation
10.12.2021 18:48
1000.00 UAH
Charity donation
10.12.2021 18:00
50.00 UAH
Charity donation
10.12.2021 11:42
100.00 UAH
Charity donation
10.12.2021 10:00
20.00 UAH
All donors

Done - reports are ready,
the project is completed.

Thank you for your support!

Done - reports are ready

Similar projects
When there are nine children in a family
Support
Health
When there are nine children in a family
Vitalii has type 1 diabetes, an incurable disease that requires careful care and nutrition for the child…
Maksym is unable to buy medicine. 4
Support
Health
Maksym is unable to buy medicine. 4
Maksym has been diagnosed with central nervous system damage. This condition significantly limits his da…
His little body cannot cope without us
Support
Health
His little body cannot cope without us
Even before he was born, doctors detected enlarged ventricles in Sasha’s brain and a cleft lip. The boy …
Let’s support Damir ahead of his 10th birthday!
Support
Health
Let’s support Damir ahead of his 10th birthday!
On March 13, Damir will turn 10 years old. He has been fighting a rare genetic condition called Apert Sy…
Show All