Levente was born in 2017 suffering from a lack of oxygen. His mother soon realised that something was wrong, as she had previously lost a child to the same rare genetic condition. Tests confirmed her worst fears: Levente has MPS II.

Since 2023, she has been attending weekly enzyme replacement therapy sessions, which she will continue to receive for the rest of her life. She also attends a special school, to which her family takes her every day with love and perseverance, so that she can have the best possible chance of development.

Levente is a cheerful, brave little boy who, despite all the difficulties, wants to enjoy the same kind of childhood as his peers.

The family is now asking for help to ease the financial burden of treatment, travel and day-to-day expenses, so that Levente can continue to receive the care he so desperately needs.

Every bit of support brings hope and security to a family that fights for their child day in, day out, out of love. ❤️