Noel and his family
For Noel, the struggle began in the autumn of 2025. Because of his clubfoot, he had to have his leg put in a cast every week for months, and then, in February 2026, he underwent a major operation. Despite the treatments and the long recovery, he always faced his difficulties with a smile and courage.
Meanwhile, the family suffered a painful loss when Noel’s beloved grandmother passed away unexpectedly. Despite their grief and the hardships they faced, they stuck together and drew strength from one another.
Today, Noel is taking increasingly steady steps in his orthopaedic shoes, but further treatment and operations still lie ahead. Every single day presents a new challenge, yet he presses on undeterred.
Noel’s story is about perseverance, love and hope. It’s about a little boy who, despite the difficulties, never gives up, and shows every day just how strong a child’s heart can be. ❤️
F. Noel and his family
Noel was born with a rare and serious muscle disease, DMD. From a very young age, his parents sensed that his journey would be more difficult than that of other children. He was not able to develop like his peers: climbing and standing up on his own was a huge challenge for him. He fell often, and as parents, each fall struck a chord. Within two years, both his legs were broken, yet he tried to stand up again and again.
Camilla and her family
Kamilla was born healthy in 2011. Around the age of 1.5, it began to become apparent that
He develops more slowly than his peers. He was diagnosed with autism at the age of 2.5 in Pécs.
chromosomal abnormality and it was determined that Kamilla had Dett syndrome. At the age of three, there was a major relapse in her condition.
Abel and his family
My little son Abel will be five years old in January. Abel has Sturge-Weber syndrome (not hereditary) and Antithrombi. He is 3 months old.
At the age of 12, he had eye surgery for glaucoma, and 12 hours later he had epileptic seizures.
They checked in on him, he had a stroke.
Vitéz and his family
Vitéz lives with autism and severe intellectual disability. His siblings, ten-year-old Gellért, who struggles with ADHD, and 11-year-old Remény, who is always there to help him, do their best to support and love each other.
G. Csenge and his family
After an uneventful pregnancy, Csenge was born. After giving birth, the family noticed that parts of Csenge's body were starting to turn blue. The parents knew that something was wrong. Csenge was transferred to the Heim Pál Children's Hospital, where her circulation collapsed. The little girl was transferred to the Gottsegen György National Cardiovascular Institute, where she underwent immediate life-saving surgery for 12 hours! (Complex Pulmonary Vein Transposition). The surgery was successful, but after the prolonged medical intervention, her little body was put under a great strain and her condition remained critical! Kidney failure, mechanical ventilation! It was a very long and stressful period in the family's life. After 3 months, they were able to go home from the hospital with regular medication.
Anna K. and her family
Anna was born premature in 2017. Since birth she has been living with cerebral palsy, which affects all four limbs with spasticity. Her life is about development - her family works every day to ensure she has the best possible development.