From the families of our ASD patients.
At six our son had maybe ten words, most of them unclear. A few months after the programme he began putting words together into short phrases. His speech therapist said it was more progress than she had seen in the whole previous year. He is communicating now, and that is what matters to us.
She looks at us when we talk to her now. She lets us hug her. She tried a new food at dinner without a meltdown. Three months on, our daughter is calmer and more present, and her occupational therapist at home confirmed the sensory sensitivity had eased noticeably.
Our son is five. He could not hold a crayon or stack blocks. After treatment his motor control improved visibly — he draws now and stands more steadily. His paediatrician in Rome told us the developmental gain was worth about eight months of typical progress.
Our son is seven and non-verbal, and we came with low expectations. Within weeks he began pointing at things he wanted, then making sounds on purpose. His sleep went from waking five or six times a night to once or twice, and the school says he is calmer and more engaged. For a non-verbal child these are enormous changes.
By eight our daughter had plateaued. The ABA, speech and OT therapists were wonderful but said they had reached the ceiling. After the programme that ceiling moved. She follows two-step instructions now, and she sat through a whole family dinner without leaving the table. Her ABA therapist said the therapy finally works the way it should.
We were honest with ourselves that autism does not simply go away, and the team were honest with us about what was realistic. A year on, our daughter handles changes to her routine far better, her language keeps growing, and she started going to a small group class near Bologna. She seems more at ease in her own skin.
Every child is different. Request a review to talk through your child's case with our medical team.







