Fondacija Jedro

For 5 boys. In 5 minutes. 5 steps. 5 smiles. 5 hugs. For "roll 5"

They want to run, to love, to learn, to push, to play, to fall in love, to jump, to hug, to throw, to catch, to solve, to get high five, to be quiet, to get ace, to to laugh, to get angry, to cheer, to sing, to dream, to rush to grow, to blow out as many candles as possible on the cake, to count…

…to stand, to sit, to smile, to breathe.

Let’s donate so that the first 5 boys with Duchenne’s muscular dystrophy travel abroad for therapy. The opportunity to travel through the Jedro Foundation is new hope, wind in the sails of all families with children suffering from this rare disease.


Let's unite, because together we can do anything.

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The „Jedro“ Foundation was founded by the families of five boys suffering from Duchenne’s muscular dystrophy with the aim of improving the health care and treatment of those suffering from this vicious disease. At the initiative of the „Jedro“ Foundation, 55 famous local musicians, actors and other public figures sang the song, and more than 100 participated in the recording of the video with the aim of raising funds for the treatment of five children suffering from Duchenne’s muscular dystrophy.


Word of the Owner and Founder

The reason for this initiative came, among other things, from the fact that I, too, am the parent of a boy who suffers from Duchenne’s muscular dystrophy.

This gave us the opportunity to come up with the idea of ​​creating the Jedro Foundation together with the parents of four other families, which we did with the help of friends and business partners and thus created a beautiful story. Considering that I have been in the cultural waters for 30 years, I thought that the best way would be to gather these people and record a song, which would draw the public’s attention to this disease.

Everything was done on a volunteer basis and we managed to do everything in a very short time. Our idea is that these will be only the first five boys and that after that we will continue to fight against this wicked disease. That’s why the action is called „five by five“, where in the future we would include other children and their families.