• About us
• Fibular hemimelia
• Treatment

The association “Prvi Korak” was founded in 2008 with a view to promote and develop activities of people with congenital disabilities of a fibular shin bone (aplasia fibula).

After the birth, the hardest thing for a child is just the First step (Prvi korak). Thanks to our own experience we help parents who are faced with such challenges.

We believe that it is precisely the experience that can provide right answer of all questions because, the best information about what's possible has the person who has passed it on his/her own.

The association was founded with no intention of making profit. If you think you are able to help us or you would like to take part in our projects, do not hesitate to contact us.

Many thanks to all of you who supported us by donations and made the treatments in specialized children clinics in Germany possible.