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
Zsombor V. and his family
Zsombor is a 3-year-old boy who is both physically and intellectually underdeveloped, yet he struggles mightily to make every small step forward. With swallowing difficulties, he has a laryngeal disorder and a feeding tube, a complex condition that requires constant attention.
Although his hearing is intact, his reactions to stimuli from the outside world are slow to develop, but the first encouraging signs are already appearing. His vision is severely impaired, but he can still follow objects, even turning his head to look at them on better days. Her body is characterised by severe muscle tension, for which she has already undergone major surgery and is currently undergoing ongoing treatment and medication. His epilepsy has returned this year after two years without symptoms.
For Zsombor, touch is the most important link to the world - it is the way to really connect with it. He loves being in the lap and is happy to participate in the development. He has recently started practising standing up and is already able to hold himself for a few moments with help - these small steps are huge achievements in his life.
In order to continue to develop and reach new milestones, he needs continuous, intensive therapy.
Please support Zsombor if you can - every help means another chance for him.
J. Milla and family
Milla is a smiling, 4-year-old girl living with a rare metabolic disease, pyruvate dehydrogenase enzyme deficiency. Her body is unable to process carbohydrates properly, so she has to follow a special ketogenic diet and gets most of her energy from fats. However, this cannot fully meet the body's needs, so its development is significantly slower: it is currently at the level of a 6-8 month old baby.
Milla's development requires ongoing, complex therapy - not only to develop her movement, but also her cognitive, sensory, vision and speech. These therapies are vital for her, but they also represent a heavy financial burden for her mother, who is raising her alone. At the moment they can spend about 100.000 HUF per month on development, which unfortunately only covers two areas.
For Milla to have a chance to develop and live a fuller life, she would also need additional therapies.
If you have the opportunity, please support Milla's development - any help will bring her closer to a better future.
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.
János Sz. and his family
Born in 2013, John has faced more challenges than many children from a very young age. His muscle weakness made him work hard for every movement, and at the age of one, epilepsy became part of his life.
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.