M. Jasmine and her family
Jasmine, a 12-year-old girl with CP, is being raised alone by her mother. She does her utmost to give her the opportunities she needs to develop, so she regularly takes her to development sessions in Dunaújváros, where they live, and to Budapest, including the Step by Step Rehabilitation Centre.
These therapies are crucial for Jasmine, but they are a heavy financial burden. As well as the cost of improvements, travel is a significant expense, which is becoming increasingly difficult for a single mother to manage.
Every day they fight to give Jasmine a chance to grow and live a fuller life.
Please support Jasmine if you can - any help is hugely appreciated
P. Lara and his family
Lara, a tiny but infinitely strong warrior, who fights more from the moment she is born than many people do in a lifetime. A toxoplasma infection has left a mark on her central nervous system - her movement and vision are damaged, she has had a shunt implant - yet every day she teaches us about true strength with a smile and perseverance.
Valeria S. and her family
Valeria, 11, has serious health problems: she is hearing impaired and has a blood disorder. Her spleen was removed when she was 6 years old and her condition requires constant medical monitoring and special attention. Her daily routine is filled with regular check-ups, treatments and precautions to ensure a safe and fulfilling childhood.
His mother is raising him and his siblings alone, and the family is in a difficult financial and living situation. It is vital for the little girl to have a stable, secure background and adequate health care.
We are now looking for supporters to contribute to the treatment, travel costs and daily needs of this little girl. All help counts. Let's help together to give her a chance for a more peaceful and secure future!
Sándor B. and his family
Alexander B is living with Duchenne muscular atrophy, a rare genetic disease that gradually weakens his muscles. He was diagnosed at the age of three. He ran and played until second grade, but now his mother pushes him in a stroller.
He has had spinal surgery and sleeps at night on a ventilator. The family lives on the third floor without a lift, so getting Sándor up and down is a physical challenge every day. His mobility is becoming increasingly difficult and their home is not barrier-free.
Sándor is a smiling, intelligent, persistent boy who is as eager to explore the world as any child. Now we need your help to make everyday life safer and more enjoyable for him.
All support brings him closer to an easier, more dignified life.
Please help Alexander if you can!
T. Zoé and her family
Zoé is only two years old, but she is already fighting a huge battle. After a long, unrelenting fever, she was diagnosed with Acute Lymphoid Leukaemia on 21 May 2025. Treatment began immediately and has been ongoing ever since.
Chemotherapy has been a difficult ordeal, and Zoe has even had to learn to walk again. She has a long road ahead of her, with active treatment followed by another year and a half to two years of maintenance therapy.
Her mother cares for her and her siblings alone, constantly commuting for treatment, while doing her best to give her daughter every chance of recovery.
Zoé, our little warrior princess, fights every day with a smile on her face. All the support is a source of hope and strength for the family at this difficult time.
Kristóf P. and his family
Born on 29 June 2023, Kristóf faced a unique challenge early in his life. He lives with a rare genetic disease called KCNQ2 - a potassium ion channel disorder that impairs his intelligence and mobility.
His development is significantly behind that of his peers and no one can say today whether he will ever be able to walk or talk independently. Every little progress has to be worked hard.
For Kristóf, regular improvements are the key: Gymnastics, physiotherapy, physiotherapy sessions, hydrotherapy and other complementary treatments help him to get the most out of his life. However, these can be a heavy financial burden for the family, with the cost of improvements and special equipment being considerable.
As parents, we do our utmost to ensure that Kristóf is given every opportunity to develop. Any support that brings us closer to helping our little boy to live his life to the fullest would be a huge help.
N. Atika and family
Atika was born in Budapest on 23 September 2022, at the 23rd week of pregnancy. Her life started with a huge struggle from the very first moments: she suffered a stroke after birth and later had to be resuscitated. She spent long months in the PICU - 112 days in total - and underwent several surgeries before she was finally allowed to go home.
As a consequence of arriving prematurely, Atika has cerebral palsy, which affects her intellectual and motor development, and her daily life requires a lot of care and assistance. She is currently attending the Pető Institute for Early Development twice a week for the third year running. She cannot yet sit, stand or walk independently, but each development brings new opportunities.
Her family is working to ensure that Atika can attend the best nursery school for her from September and lead a more independent and fulfilling life in the long term. They are now asking for help to do this - so that Atika's journey continues to be one of hope, care and opportunity.
M.Lotti, M.Máté and family
Matthew is just 6 years old - a happy, loving little boy, full of life and smiles.But on 25 September 2025, the family's life changed in an instant
Lotti is a beautiful 9-year-old girl who has been a fighter since birth. She came into the world with a cerebral ventricular enlargement, which has slowed her development, made it difficult for her to move and she needs a lot of help in her daily life.
L. Jasmine and her family
Jasmine arrived on 28 May 2023, but her joy was soon overshadowed by the news that one of the twins, Jasmine, was born with neuroblastoma. Since then, they have undergone countless surgeries and chemotherapy treatments and will spend most of their lives within the walls of the hospital.
In addition to Jasmine, there are four other minor children in the family, including her twin sister Nazéra. Due to ongoing treatments and hospital stays, the father is currently unable to work as the children cannot be left unattended.
The family is in an extremely difficult situation, both emotionally and financially. Any support will be a great help to them at this trying time. Thank you for helping to give Jasmine and her family hope for the future.
B.Donat and his family
B. Donat, Dodo is a real little fighter. He was born at 28 weeks' gestation by a life-saving Caesarean section and suffered two massive strokes after birth. The difficult start mostly affected his movement, but Dodo is still a very smart, naked-hearted boy with a huge will and zest for life.
Every day is filled with developmental activities: hydrotherapy, manual therapy, conductive development at the Pető kindergarten, where the daily commute means a long journey. His family is doing their best for him - intensive rehabilitation and regular medical check-ups are helping him to achieve his goal of walking independently, even with the help of an assistive device.
But the most important thing is that ongoing treatment can prevent more serious musculoskeletal problems later on. Every therapy is another chance for Dodo - a step towards a lighter, freer childhood.