Ákos & his family
Ákos was born on September 5, 2021, at 31 weeks, prematurely. This is the first time in his life
his moments were also filled with struggle. On the second day, he suffered a severe stroke, which began a long period of rehabilitation. Margit Hospital newborn for three weeks
we were with him in his ward before we could take him home, and the series of intensive therapy treatments that have continued ever since began.
Marcel and his family
Marcell arrived prematurely into a family where his two adult brothers were eagerly awaiting his arrival. He developed beautifully in the first month and made his entire family happy with his smile. At just 13 months old, he was already saying words, reciting his favorite rhymes, playing mischievously, and was a joy to watch. He played functionally with his toys, walked nicely, and ate and drank independently.
Zs. Léna and her family
Lencsi was born in 2016 as a completely healthy baby. His motor development had always been slower, but at the age of one and a half his development stopped and reversed. Genetic testing showed he had SMA type 2.
B. Jasmine and her family
It was an incomparable, wonderful moment when we could hold our healthy newborn baby girl in our arms. Our happiness was boundless that our family was complete with the arrival of Zoé. However, life had a difficult path for her. Eleven months. That was all we had from our carefree, joyful childhood.
B. Krisztián and his family
Krisztián, 20, with severe mental retardation and marked behavioral deterioration,
He lives with secondary Parkinson's disease in Marcali. Due to his condition, he regularly takes medication on the advice of a specialist. Unfortunately
not housecleaning, needs help with dressing and shaving
also. He can go to the toilet, but is unable to take care of himself independently. When eating alone
uses the spoon. His only occupation and amusement is to listen to a lot of music
is silent.
Sidonia and her family
Sizdónia was born prematurely on June 12, 2008, at 27 weeks, with a lack of oxygen. The diagnosis is infantile paralysis, which severely affects his psychomotor development. In addition, he still struggles with locomotor problems, psychological and learning disorders.
B. Marcell and his family
Marcell was born naturally at 37 weeks, with an Apgar score of 10/10.
After his birth, he was immediately transferred to the neonatal unit because his breathing was very rapid.
At the age of 16 months, Marcin had an epileptic seizure, which was followed by several in the hospital. He received medication, but unfortunately he was unable to completely stop the seizures, and he often lost consciousness.
Maja & Mário
Maja and Márió are brothers and sisters who need support.
Maja, only three years old, is battling ganglion neuroblastoma, a rare and serious cancer. The treatments – surgeries, chemotherapy – take a toll on the little girl and her family, but they are driven by the hope of recovery. All support is essential to ensure the best medical care.
D. Levente and his family
Levi is a young boy with autism and severe ADHD who is being raised alone by his mother. Levi requires constant, 24-hour supervision and even the simplest activities are difficult for him.
After long hospital stays, his condition has partially improved, but he still needs improvement and regular support. He attends school on an individual timetable, his meals are highly selective and his involvement in everyday situations is difficult.
His mother is unable to work, while medicines and improvements are a significant financial burden. She also has medication that costs tens of thousands of forints a month and is not subsidised.
Their budget for improvements is now being exhausted.
Please support Levi if you can - every help gives him a chance to improve and have a better life.
Olivia & her family
My name is Anita Tóth, I moved to Budapest from a small town in Szabolcs, Pap, for work opportunities. My little girl, Olívia Tóth, was born on January 24, 2023, but she had serious health problems at birth. It turned out that she suffers from a rare genetic disease, Vein of Galen malformation, which caused circulatory failure, heart failure and stroke. She underwent several surgeries and was in danger of dying for many months.