A child born with cleft lip and palate, a condition commonly referred to as kōshin kōgai-retsu in Japan, finds hope in a potential treatment found by the parents. The article covers their journey, the discovery of the new medical possibilities, and the child's ongoing recovery process. The story highlights the perseverance of the child and the parents' relentless pursuit of happiness for their offspring.

In Japan, there's deep compassion and collective societal effort towards individuals afflicted with congenital disorders like cleft lip and palate. The focus is usually on finding advanced medical solutions, as well as providing psychological and emotional support. Children with these disorders usually receive free surgical treatments from the government in an effort to integrate them fully into society and improve their quality of life.

Much like in Japan, the EU and US also offer robust healthcare support for individuals with cleft lip and palate. Early surgical intervention, speech therapy, and long-term dental care are commonly provided. In the US, charitable organizations often conduct free operations for children from low-income families. Meanwhile, the European Cleft Organization coordinates high-level professional medical, educational, and psychosocial care across the EU.