Milla is a smiling, 4-year-old girl living with a rare metabolic disease, pyruvate dehydrogenase enzyme deficiency. Her body is unable to process carbohydrates properly, so she has to follow a special ketogenic diet and gets most of her energy from fats. However, this cannot fully meet the body's needs, so its development is significantly slower: it is currently at the level of a 6-8 month old baby.

Milla's development requires ongoing, complex therapy - not only to develop her movement, but also her cognitive, sensory, vision and speech. These therapies are vital for her, but they also represent a heavy financial burden for her mother, who is raising her alone. At the moment they can spend about 100.000 HUF per month on development, which unfortunately only covers two areas.

For Milla to have a chance to develop and live a fuller life, she would also need additional therapies.
If you have the opportunity, please support Milla's development - any help will bring her closer to a better future.