Ryan was born in August 2015 after a normal pregnancy and a normal delivery.At the age of two months when his parents went to vaccinate him, the doctor noticed that

We are pleased to share a story of a lovely family from Berlin who is in the process with us at First-Step. They first contacted us when their eldest son

After a few months, his parents began to notice a developmental delay and he was diagnosed with hypotonia, after further tests a genetic defect was discovered.The family contacted First-Step after

‘First Step’: an Israeli therapy enabling optimal child development May 2010. Mila, aged 2 and a half, is about to leave Switzerland with her parents. Direction: Israel. The purpose of

Emma was born with Cerebral Palsy. When we first met Emma she was three, and hardly used her arms and legs. A few months later, she was able – for

Alicia was born with Sturge-Weber syndrome – which appears in the centralnervous system, a facial birthmark, and partial deafness. Alicia was hospitalised at a very young age, and underwent several surgical

Giovanni was born with Wolf-Hirschhorn syndrome, which presented in Giovanni as extensive developmental and language delays. When we first met him at the age of 2 and a half, he

The story of Mila according to the parents: “Mila was born on 1 July 2013 after a so-called normal pregnancyand by vaginal delivery with epidural.At birth all seemed normal, except

Lias, a boy from Switzerland who’s almost 5, was diagnosed with Cerebral Palsy, epilepsy and low muscle tone.With the support of the KMSK association, the family started the First-Step therapeutic process in Switzerland and later came

Benedikt from Switzerland was born with Wolf-Hirschhorn syndrome. When Benedikt was 2 years old, the family has started a therapy with First Step method. Since then – Beni continues to improve.

Davide is a child of two and half, from Switzerland. Originally his family was from Italy. He was born after 42 weeks of pregnancy in a caesarean delivery. Right from

Matteo Ferrandi was born in May 2012 in Italy, to a loving family, with two older sisters.Some days later, tests revealed that he had STXBP1 syndrome. In his first year,

Margherita from Italy was born with a genetic mutation of the KCNQ2 gene, and epilepsy.When we met Margherita at the age of two years, she didn’t like to stay on

Giorgia was born on September 2015 in Rimini – Italy Her developmental growth was slow than normal and at the age of 5 moths she was diagnosed with Wolf-Hirschhorn Syndrome.