My daughter Hana, two years old, was born with a rare genetic disorder – Prader-Willi Syndrome (PWS). This condition affects her growth, development, appetite, and daily life. She needs constant supervision, a special diet, and regular therapies in order to have a chance at a healthier and happier life.

Our little girl is cheerful, strong, and full of love, but her journey is filled with challenges. Every day is a struggle – a struggle to provide her with the care she so desperately needs.

Sadly, the national health fund does not cover all of the therapies she urgently needs, and these private treatments are crucial for her progress and quality of life.

In addition to these challenges, our family is also facing financial difficulties. We live in a rented apartment, and at the moment only the mother is working to support the household. A large part of our income goes toward rent and basic living expenses, leaving very little for the therapies that are so important for our daughter’s development.

All donations will go directly toward:

private physical therapy

speech and occupational therapy

additional specialized programs recommended by doctors but not covered by public healthcare

That is why I am reaching out to you, from the bottom of my heart, asking for help. ❤️

Your support, your donation – no matter how small – will make a huge difference for Hana. It will allow her to receive the therapies and care that are vital for her life.

If you are not able to donate, please consider sharing our story. Every share brings us closer to someone who might be able to help.

Thank you, from the bottom of my heart, for standing by us, for standing by our little girl, and for giving us the strength to keep going. ❤️