Chrysallida

Support – Awareness – Hope for children and families affected by clefts and craniofacial anomalies

The Chrysallida Association was founded to provide financial and psychological support to children and adults with clefts and craniofacial anomalies, as well as to their families.
At the same time, we aim to make a meaningful and organized impact on decision-making bodies involved in the treatment of these conditions, advocating for every child's right to complete and high-quality care from the earliest stages of life.

Our Vision

Smiles Filled with Hope

Cleft lip and/or palate is one of the most common conditions a child can be born with. While it was once surrounded by social stigma and misunderstanding, today, medical progress and the teamwork of specialized professionals make successful treatment and full recovery possible.

Together, we can transform every challenge into a life-changing smile. At Chrysallida, we turn anxiety into action and uncertainty into hope.

How We Help

Here’s what we aim to achieve:

1. Providing support to families from other parents who have gone through similar experiences.
2. Offering information and education about treatment, unique challenges, and daily life.
3. Advocating for rights and giving families a voice with the State and relevant authorities.
4. Improving healthcare services and access to comprehensive treatment.
5. Raising public awareness about differences and the possibilities for recovery through modern medicine.