Testimonial

This year, our family had the opportunity to take part in the Lignano Intensive Week for the very first time.

Written by Julian (Aleix's father) Our son Aleix, aged 9, has been diagnosed with Duplication Syndrome of the

Written by Ana, Jan's mum Dear readers,Today I'd like to tell you about our positive experience of Adeli therapy

Written by Micki, Luzia's mum Luzia is an extraordinary child. She has an unbalanced translocation between two chromosomes,

Written by Jeannine, Ben's mum This year, Ben's rehabilitation took place in May at Kokon.

Written by Jasmin (Leon's mum) Leon is 5 years old and lives in Germany. Last May, he had

Although there is currently no treatment for MECP2 gene duplication syndrome, daily training remains very important for

A day in the life of a family with MECP2 gene duplication syndrome (written by Sasha Gersohn) The

Prokop family: We are Jeannine, Michael, Emma (4) and Ben (1). We will soon be living in Upper Austria