Márk was born on December 11, 2014, 8 months premature, and his life journey began with a quick home birth. The pregnancy and the first year passed without any problems, but over time, worrying changes began to appear. From the age of one, Márk's development slowed down, and a neurologist diagnosed him with hypoxia and developmental disorders.

He also developed severe epilepsy, which affected the entire brain and, unfortunately, could not be treated with surgery. In recent years, Márk has undergone several treatments, including infusion and injection therapies, as well as the introduction of a new anti-epileptic drug. Thanks to his perseverance and the love of his family, Márk's condition has improved and he is currently seizure-free and has a developmental teacher at home to help him develop.

Currently, Márk suffers from Rhett syndrome, astatic myoclonus epilepsy and atypical absence seizures, and the family would like to provide him with the necessary developmental activities. Márk's interest in poems, rhymes and songs encourages them to provide him with even more opportunities for development.

They hope that through the power of the community and support, they will find solutions that will improve the quality of life for Márk and his family.

Let's support the family so they can be part of Márk's development and recovery!