Sz. Jazmin and her family
Jasmine often had pneumonia and was suffering from pain in her right lung. In 2013, they went for an X-ray, where a walnut-sized shadow was visible on the lower lobe of her lung, which grew to the size of a palm in a short time. The usual examinations began. For a long time, the doctors did not know what it really was. On 05/09/2013, it was time for surgery. Jasmine was only 10 years old when the lower 1/3 of her right lung lobe was removed during the operation.
K. Szofi and her family
Sófi was born prematurely at 27 weeks, weighing 990 grams. She was not breathing spontaneously at birth and suffered a stroke shortly after. Due to her respiratory failure, she was on mechanical ventilation for a long time. As a result of the stroke, the cerebrospinal fluid could not drain properly, so a shunt was implanted.
T. Áron and his family
After winning the football championship, on a summer day in 2021, 17-year-old Áron Thuróczy rushed to the Körös beach with his friends to celebrate. Áron jumped into the water, but his head hit an underwater object, which immediately paralyzed him. After a long treatment, Áron is in better physical condition and is doing everything he can to make his recovery as successful as possible.
K. Wenceslas and his family
Wencel is a cheerful, always smiling little 1.5-year-old guy, about whom no one in the world would say that he has any health problems. Unfortunately, this is only an appearance for now. Wencel came into the world with a serious complex heart defect, transposition of the great arteries, that was not discovered during pregnancy. The parents expected a completely healthy baby, as his condition in the womb showed no signs of any problems.
Attila T. and his family
Attila was born completely healthy. At the age of 6 months, his mother indicated to the health visitor and the pediatrician that Attila was lagging behind compared to his peers. He did not lift his head, did not push himself out or turn around, he just lay there. The tests began - skull MRI, audiological examination, genetics, ophthalmology, hearing test,) all the results were perfect, yet they did not know what could be wrong with the little children. The result was a neurological examination, where they received the diagnosis: Epilepsy and Ataxic Cerebral Palsy, which affected the speech and movement center to such an extent that Attila was unable to walk and communicated by pointing.
Kata and her family
Kata was born completely healthy on September 6, 2002. Her illness began with an epileptic seizure. She was diagnosed with encephalitis in the hospital.
He got better and better, and after 2 weeks they took him off the diuretic medication and his left side became paralyzed, then it turned out that he had an overproduction of cerebrospinal fluid.
The family was living in Jász-Nagykun Szolnok County when the overproduction of cerebrospinal fluid was discovered. They were taken to the Budapest National Neurosurgery Hospital, where Kata underwent endoscopic brain surgery.
Thomas and his family
Tomi was born in 2016. Soon after his birth, it was discovered that he had a serious heart defect and was suspected of having Down syndrome. When genetic testing confirmed the diagnosis of Down syndrome, his biological parents decided they could not raise him.
Csaba L. and his family
Csaba has been living with severe mobility impairment since birth due to a medical error. Labor began in the 33rd week of pregnancy, and the mother's doctor thought it best to delay it with a new type of infusion at the time. The delay was so successful that the doctors finally induced labor in the 41st week.
Veda and her family
Véda was born at 36 weeks by emergency cesarean section, due to undetected toxemia of pregnancy. She suffered from a lack of oxygen in the womb, and unfortunately suffered a brain hemorrhage on the 6th day after birth.
Levente L. and his family
His needs and the way he is treated are both special. Since childhood, he has been continuously ensured that he can live a life as free from obstacles as possible, in accordance with his condition. This fact requires both human and financial sacrifices on the part of the family: his mother can only work part-time, and the creation of Levente's environment requires specific, special solutions, which are sometimes difficult to finance financially - especially in the case of an older son with severe adolescent autism, as a single mother, raising another child who is also a teenager.