It is his mission to reach out to all children seeking medical attention who is unable to afford medical treatment costs.
Roman keeps working hard to earn more funds to send more children for medical treatments around the world. Here is a partial list of the children whom Roman has successfully sent for medical or surgical treatments.
Bartuś, Michał suffers from HLHS. To keep him alive, he had to undergo three surgeries. Because the parents found out very late about the boy’s illness, there was no time to lose, the boy needed surgery right after birth.
Thanks to Foundations support, the boy underwent surgery successfully and today he is a happy three-year-old.
Wiktoria, Kubuś suffers from Leigh syndrome, an incurable genetic disease. The first symptoms appeared when the boy was only 1.5 years old. He stopped developing, and over time he began to lose the skills he had already mastered.
He stopped walking and talking, and within six months he became a lying down child. Futurenet Foundation wanted to improve Michałek’s standard of living, therefore funding an electrostimulation. With its help boy started swallowing on his own.
Kubuś was suffering from HLHS, the most severe heart disease. The world turned upside down, and the fight against time and collecting money for the first of three operations to save Kubuś’s life began. Of course, Futurenet foundation couldn’t stay indifferent.
Not only did we manage to collect the missing amounts for two out of three operations, but we also succeeded perfectly. Today the boy is almost three years old, he is developing properly, and he has become a fitter, stronger, and more temperamental little man. He is very cheerful every day and infects everyone with his smile.
Ala was born with a dislocated hip and reduced muscle tone. Daily rehabilitation helps her overcome new barriers but does not ensure full fitness.
Thanks to our support, it was possible to purchase orthoses for the girl. They protect the foot and have an extensor under the knee that straightens the contracture in her leg. Over time, the orthosis will help the girl stand on her own feet.
Basia is another ward of the Foundation. The girl also has Leigh’s syndrome, we are very happy that we managed to purchase a specialized car seat for her, which will improve her driving comfort during long trips for rehabilitation.
Natalia was born with spina bifida and concomitant internal hydrocephalus. The first diagnoses were devastating – the girl was not supposed to walk and was not developmentally. However, as it turned out, there was hope.
The girl needed knee surgery, elimination of contractures, as well as lengthening of the tendons in the groin. Thanks to the Foundation’s help, the girl went to surgery, which gave her hope to be independent in the future.
Wiktoria was born a healthy child, unfortunately, this changed at the age of 2. She’s started to have back problems. For a long time, doctors did not know what was causing the problems. It wasn’t until the age of 11 that doctors in Spain diagnosed abnormalities in the end thread of the spinal cord.
Spinal cord surgery is not performed in Poland, therefore we did everything in our power to get Wiktoria to go for surgery in Barcelona. Thanks to the operation, the girl has greater mobility and much fewer limitations in everyday life.
Bartek was born without a tibia and, despite his young age, has already undergone several operations and hours of rehabilitation in his life. Thanks to the Futurenet Foundation leg and knee surgery was performed by doctors from the Paley Institute in the USA.
We covered a large part of the costs, thanks to which Bartek flew for an operation that drastically changed his standard of living and independence.
Daniel suffered from cerebral palsy and optic nerve hypoplasia. The boy is blind, and from the age of 6 months, he commuted with his parents to therapy in distant Wrocław, where the only specialist equipment in Poland is located.
Foundation decided to buy amblyopia, thanks to which he can be rehabilitated every day at home.
Miłosz suffers from arthrogryposis – a very rare disease that causes contractures and deformities of the limbs. The causes of this disease are unknown, and it occurs once in 10,000 births. As a result of the disease, the boy has deformed lower and upper limbs. From the very beginning of his life, the only chance the doctors gave him was to use a wheelchair.
The boy’s extraordinary determination and the Foundation’s financial support made it possible to perform a very important foot operation, which brought Miłosz closer to fulfilling his dream – playing football without anyone’s help.
Kacper was born with a congenital defect in the right hand. The family’s financial problems did not allow the boy to buy a prosthesis. As soon as we found out about it, we couldn’t stay indifferent and immediately started to help.
Foundation found the means, ordered a prosthesis, and in the end, the boy’s smile said more than a thousand words.
Story of Oluś was very heartbreaking and emotional for us The boy was born with a serious disease of the right leg. Thanks to FutureNet Foundation treatment in the USA was possible!
Oluś had his third surgery in October. During the surgery, the doctors took off his braces, which he had been wearing since June. Now his leg is stiffened in a plaster.
The boy started intensive rehabilitation, during which he learns to walk again. Over the last six months, his leg has become much longer and straighter! We keep our fingers crossed for further treatment of Oluś!
Story of Oluś was very heartbreaking and emotional for us The boy was born with a serious disease of the right leg. Thanks to FutureNet Foundation treatment in the USA was possible!
Oluś had his third surgery in October. During the surgery, the doctors took off his braces, which he had been wearing since June. Now his leg is stiffened in a plaster.
The boy started intensive rehabilitation, during which he learns to walk again. Over the last six months, his leg has become much longer and straighter! We keep our fingers crossed for further treatment of Oluś!
Jaś was 2.5 years old when he fell ill with type 1 diabetes, since then he has been fighting the disease every day, 24/7. He must have his blood sugar checked every two hours.
His parents had an old-generation insulin pump that did not record or analyze results. Thanks to our support, a new pump was purchased for Jaś.
