[{"data":1,"prerenderedAt":823},["ShallowReactive",2],{"home-blog-blog_en":3,"home-campaigns-kampanyok_en":285},[4,128,254],{"id":5,"title":6,"body":7,"category":116,"date":117,"description":110,"excerpt":118,"extension":119,"image":120,"meta":121,"navigation":122,"path":123,"seo":124,"slug":125,"stem":126,"__hash__":127},"blog_en\u002Fen\u002Fblog\u002Fout-of-my-mind-amit-egy-film-megtanithat-nekunk-a-nem-beszelo-gyerekek-belso-vilagarol.md","Out of My Mind – What a Film Can Teach Us About the Inner World of Non-Speaking Children",{"type":8,"value":9,"toc":109},"minimark",[10,15,23,30,33,37,43,46,49,52,56,59,62,65,68,73,78,88,95,102],[11,12,14],"h2",{"id":13},"the-film","The film",[16,17,18,22],"p",{},[19,20,21],"em",{},"Out of My Mind"," (2024) is a Disney+ original film based on Sharon M. Draper's international bestselling novel of the same name. Directed by Amber Sealey with a screenplay by Daniel Stiepleman, it premiered on Disney+ on November 22, 2024 — where it is also available in Hungary with a subscription.",[16,24,25,26,29],{},"The story centers on Melody Brooks, a sixth-grade girl with cerebral palsy: she cannot speak and uses a wheelchair, yet she has a sharp mind, a photographic memory, and an extraordinarily rich inner world. For a long time, the people around her — her teachers, her classmates, sometimes even her own family — judge her by what she ",[19,27,28],{},"cannot"," show of herself: her movement, her speech. When a young teacher recognizes the talent within her and Melody joins the mainstream curriculum, the film unpacks exactly what its title promises: that what someone says matters far more than how they say it.",[16,31,32],{},"One of the film's boldest directorial choices is that Melody's inner voice — her thoughts, her humor, her anger, her joy — is voiced by Jennifer Aniston. This is no gimmick: it literally lets the viewer into the mind of a non-speaking child, offering a perspective we rarely get in everyday life. The film debuted at the 2024 Sundance Film Festival and went on to win a Peabody Award, with critics highlighting how it manages to sidestep the trap of so-called \"inspiration porn\" — it doesn't try to move us by casting its disabled protagonist as automatically heroic, but by building a real, authentic character.",[11,34,36],{"id":35},"why-this-matters-to-us-parents-raising-children-with-cp","Why this matters to us, parents raising children with CP",[16,38,39,40,42],{},"Raising a child living with cerebral palsy means confronting, day after day, the fact that most of the world judges by speech, by movement, by \"typical\" behavior. ",[19,41,21],{}," shines a light into exactly this blind spot. It shows that inside the mind of a non-speaking child there can be a world of thought just as rich, complex, funny, and sensitive as anyone else's — it simply reaches us through different channels, or doesn't reach us at all if we fail to offer enough attention and the right tools.",[16,44,45],{},"One mother's reflection: \"For me, this film was a genuine eye-opener. Not because it told me anything new about my child having an inner world as rich as any of her peers — as a parent, I knew that, of course — but because we so rarely get such a direct, cinematic glimpse of what all this might look like from the inside. It reaffirmed what I feel every single day: children with CP are exactly like any other kid — only the path of communication is different.\"",[16,47,48],{},"The film struck a familiar chord in another way as well. It shows how the system — whether school, healthcare, or social services — almost always looks for the simpler, more convenient path. Not out of malice, but because individualized attention, genuine integration, and providing the right tools demand resources, energy, and commitment. As a result, parents very often have to fight hard battles to secure the education, help, and support that truly fits their child.",[16,50,51],{},"What is especially sobering: all of this takes place in — and holds true for — the United States, a country where cerebral palsy is well known, well researched, and lived by many families. If securing the right support is such a struggle even there, how much harder must it be in Hungary, where many people have never even heard of CP, let alone understood its everyday reality.",[11,53,55],{"id":54},"why-we-recommend-it-to-others","Why we recommend it to others",[16,57,58],{},"This film has something to offer in three directions.",[16,60,61],{},"For parents of children with CP, it offers reassurance that we are not alone in the battles we fight — with the system, with institutions, sometimes with our own surroundings — so that our child gets a chance. And it reaffirms that our child is exactly like any other child — they simply communicate differently.",[16,63,64],{},"To children and young people living with CP, it says that they are not defined by their movement or their speech — but by their thoughts, their humor, their personality. That they are immeasurably cool, exactly as they are.",[16,66,67],{},"And for everyone else — teachers, healthcare professionals, or simply anyone who wants to better understand the world of people living with disabilities — it offers a rare, authentic, cinematically crafted view from inside the mind of a non-speaking child.",[16,69,70,72],{},[19,71,21],{}," is available to stream in Hungary with a Disney+ subscription. If you have the chance, it is well worth watching — and if there is a child or adult living with CP in your life, it is worth watching together with them.",[16,74,75],{},[19,76,77],{},"Sources and further reading:",[16,79,80,81],{},"· ",[82,83,87],"a",{"href":84,"rel":85},"https:\u002F\u002Fen.wikipedia.org\u002Fwiki\u002FOut_of_My_Mind_(film)",[86],"nofollow","Out of My Mind (film) – Wikipedia",[16,89,80,90],{},[82,91,94],{"href":92,"rel":93},"https:\u002F\u002Fpress.disneyplus.com\u002Fnews\u002Fdisney-plus-out-of-my-mind-trailer-and-key-art-world-cerebral-palsy-day",[86],"Disney+ Press: official trailer and background material",[16,96,80,97],{},[82,98,101],{"href":99,"rel":100},"https:\u002F\u002Fvariety.com\u002F2024\u002Ffilm\u002Freviews\u002Fout-of-my-mind-review-1236224837\u002F",[86],"Variety review",[16,103,80,104],{},[82,105,108],{"href":106,"rel":107},"https:\u002F\u002Fwww.indiewire.com\u002Fcriticism\u002Fmovies\u002Fout-of-my-mind-review-disney-plus-movie-1235066347\u002F",[86],"IndieWire review",{"title":110,"searchDepth":111,"depth":111,"links":112},"",2,[113,114,115],{"id":13,"depth":111,"text":14},{"id":35,"depth":111,"text":36},{"id":54,"depth":111,"text":55},"figyelemfelhivas","2026-08-07",null,"md","\u002Fimages\u002Fpages\u002F01KZEJ4KP1XGACEYJHE05PRMK5.png",{},true,"\u002Fen\u002Fblog\u002Fout-of-my-mind-amit-egy-film-megtanithat-nekunk-a-nem-beszelo-gyerekek-belso-vilagarol",{"title":6,"description":110},"out-of-my-mind-amit-egy-film-megtanithat-nekunk-a-nem-beszelo-gyerekek-belso-vilagarol","en\u002Fblog\u002Fout-of-my-mind-amit-egy-film-megtanithat-nekunk-a-nem-beszelo-gyerekek-belso-vilagarol","lcqVtqkB7jdTcG4ZMxlPudBkjGnylIgefRr5IWUhZp8",{"id":129,"title":130,"body":131,"category":116,"date":246,"description":135,"excerpt":118,"extension":119,"image":247,"meta":248,"navigation":122,"path":249,"seo":250,"slug":251,"stem":252,"__hash__":253},"blog_en\u002Fen\u002Fblog\u002Fa-gurulo-tanarno-az-elre-tor.md","The “Rolling Teacher” Takes the Lead",{"type":8,"value":132,"toc":244},[133,136,142,145,150,153,156,161,164,169,172,175,178,183,186,189,192,197,200,203,208,211,214,219,222,227,230,235,238,241],[16,134,135],{},"Mária, our newest volunteer, was diagnosed in infancy with what was then called Little's disease — known today as cerebral palsy (CP). In many ways, Mária has been a trailblazer: she attended mainstream schools alongside non-disabled children her whole life, she was the only student with a physical disability to complete the library science and Hungarian literature program at her college's faculty of education, and she even went to freshman camp to prove that a full life is possible this way too. We sat down with the “rolling teacher” to talk about what it was like growing up with CP in the 1990s and what challenges she faces in everyday life.",[16,137,138],{},[139,140,141],"strong",{},"When did your parents realize that movement would be harder for you than for others?",[16,143,144],{},"F.M.: I wasn't moving the way an infant my age should, so my parents took me to the developmental neurology clinic in Pécs when I was 9 months old. The medical diagnosis there was a severe motor and cognitive impairment — even though I had been discharged from the maternity ward in Pécs as a healthy baby, simply born premature. After that, we attended the pediatric neurology clinic in Szekszárd until I was 2, and then I was referred to the Pető Institute (ed.: an institution dedicated to the rehabilitation of people with motor disabilities). That's where we received the final diagnosis: spastic diplegia, combined with severe Little's disease.",[16,146,147],{},[139,148,149],{},"How well known was this condition in Hungary in the 1980s — then called Little's disease, today cerebral palsy?",[16,151,152],{},"F.M.: I wouldn't say it was completely unknown, but people didn't really understand it. The health visitor and the doctors reassured my parents that I would catch up with my peers in time. They said that the proverbial thread holding me back from stepping and walking would snap one day, and I'd be able to walk on my own. The developmental neurologist was the first to notice that something was wrong.",[16,154,155],{},"Once my parents learned the diagnosis, we went regularly to the Pető Institute for movement therapy as an outpatient — at first every six weeks, later every three months — until I was 13 or 14. I wasn't a boarder, and my parents didn't want me to be. Then we found a kindergarten relatively close to us, where a wonderful conductor worked with me. Thanks to her exercises, my movement improved dramatically: she was the first to teach me to walk, first with two tripod canes, then with two single-point canes — and by the time I started primary school, I had switched to two single-point canes.",[16,157,158],{},[139,159,160],{},"Did you face any disadvantage in primary school because of your physical disability?",[16,162,163],{},"F.M.: My parents did everything — and still do to this day — so that I could take part in everything the other children did. Whether it was a kindergarten or school trip or any community program, I never felt left out. The only negative was the occasional teasing from other kids, but I never experienced that as a tragedy. I always went to school with non-disabled children. In first and second grade I found a very welcoming community, and later, when we moved to Kakasd, I didn't have any particular trouble fitting in there either. Hats off to my teachers, too — I loved learning. Math and the various practical subjects weren't my strengths, but Hungarian and the world of books certainly were.",[16,165,166],{},[139,167,168],{},"How much was it down to luck, and how much to your parents' persistence, that you didn't end up in a special school for children with motor disabilities after kindergarten? Was it common in the 90s for a child with Little's disease, with CP, to be in a class with non-disabled students?",[16,170,171],{},"F.M.: It's true that my parents fought their own battles in those days. The county learning ability assessment board didn't recommend admitting me to a mainstream primary school, so we turned to the national assessment board to have the expert opinion overruled. The test results proved that I was capable of starting primary school. That's how I got into Primary School No. 2.",[16,173,174],{},"It also came down to the goodwill of the principal there. He was very kind, and he said no paperwork was needed — the little student would prove herself. He even asked my parents whether I needed any special equipment — a desk, a chair, or an assistant during breaks — because he would arrange that too. These things weren't really provided for students with motor disabilities back then.",[16,176,177],{},"Of course there were difficulties — for example, we had to request an expert opinion for art class so I wouldn't get a bad grade — but things like that can happen to anyone. Above all, I owe it to my teachers' positive attitude and my parents' outlook that I could attend a mainstream school. They didn't hide me away from the world; they took me everywhere and stood up for me.",[16,179,180],{},[139,181,182],{},"What were your high school and college years like in this respect? Were you able to enjoy that period?",[16,184,185],{},"F.M.: I went to high school in Budapest, at the state institute for people with motor disabilities. That's where I got my three-wheeled electric moped, which gave me a great deal of freedom. We received plenty of developmental support, but disabled and non-disabled students were still in the same class. That was a great community too, though we drifted apart when I went off to college.",[16,187,188],{},"Later, at the faculty of education in Kaposvár, I was the only student with a motor disability in the library science and Hungarian program who took on full-time study. There, too, I was in a pioneering role — proving that a degree can be earned in this condition as well.",[16,190,191],{},"And I even went to the freshman camp! I remember that during the first icebreaker rounds, I said that right now anyone could ask me anything about my disability — but for the remaining 4–5 days I didn't want to hear about it, because I wanted to be a full member of the team. That was a big step at the time, but I had a wonderful time. When I went to the opening ceremony, several people recognized me and said hello. Since finishing university I've been working in my profession, in a school library in Szekszárd.",[16,193,194],{},[139,195,196],{},"How do students and teachers treat you day to day?",[16,198,199],{},"I get along very well with the high schoolers — they approach my condition completely naturally. At school, since the distances are long, I use my moped. That's why some of the students call me the “rolling teacher.” In the library, I get around with my canes.",[16,201,202],{},"My experiences are fundamentally positive: students and colleagues alike are accepting, and after a few encounters they become even more open. I do the work I love, and I face no negative experiences or disadvantages. The everyday struggles are there, of course — but everyone has those.",[16,204,205],{},[139,206,207],{},"How easy is it for you to get around in Kakasd? Is accessibility ensured, or is there local transport for people with motor disabilities?",[16,209,210],{},"F.M.: When it comes to accessibility, we're at quite a disadvantage — nationwide and in our area alike, I think. The school where I work is easy to reach in that respect. But there's no train service here, and because of my condition I can't use public transport anyway.",[16,212,213],{},"Transport for people with motor disabilities isn't provided in the area. Twice I requested the transport service from the local care center when I was filling in at the library in Bonyhád. I ended up seriously late — not half an hour, but an hour and a half — because there was no reliable arrangement for when and how they would come for me. That's when we decided this wasn't going to work. Currently my father drives me to work every day. That's also why I keep looking for options — because if my parents can no longer take me back and forth, I'll have to solve it myself.",[16,215,216],{},[139,217,218],{},"What are the financial implications of therapies and developmental treatments for an adult with CP? To what extent does the state support you?",[16,220,221],{},"F.M.: Since high school, I haven't received any state-funded developmental treatment or therapy. As I see it, most of the effective therapies are only available privately. State-funded physiotherapy is only provided if I'm on sick leave. That amounts to 14 sessions twice a year, each requiring a separate prescription, and each session is 20 minutes. Being on sick leave for the duration of the physiotherapy is a bigger financial loss for me, so I'd rather not use it unless I have to.",[16,223,224],{},[139,225,226],{},"Based on your experience, how do you think cerebral palsy is perceived in Hungary?",[16,228,229],{},"F.M.: We have an enormous task ahead of us in raising awareness. What I often experience is that when I enter an unfamiliar environment and that openness isn't there, people don't know how to approach me.",[16,231,232],{},[139,233,234],{},"Why did you join the Independent Steps Foundation?",[16,236,237],{},"F.M.: I joined because I see that people living with CP receive support primarily in childhood. Adult aftercare, guidance, and advocacy, however, often disappear after a certain age — even though they would still be very much needed later on.",[16,239,240],{},"I believe it's important to have a community and advocacy organization that also helps adults with CP, informs them about therapy options, and offers guidance. I myself am constantly seeking out and trying different therapies, but they demand significant money, time, and energy.",[16,242,243],{},"For people living with severe motor disabilities, accessibility, travel, transport, and organizing mobility are also serious challenges. These tasks often fall on family members. I believe it's important that, with the right support, we can live full lives as adults even when family help is no longer behind us.",{"title":110,"searchDepth":111,"depth":111,"links":245},[],"2026-08-01","\u002Fimages\u002Fpages\u002F01KYY9V96HRFJD0V0C63NNK1M7.jpg",{},"\u002Fen\u002Fblog\u002Fa-gurulo-tanarno-az-elre-tor",{"title":130,"description":135},"a-gurulo-tanarno-az-elre-tor","en\u002Fblog\u002Fa-gurulo-tanarno-az-elre-tor","tuGFapiHlcEOE4an6z5kr9GpPYaSu50e57yyXguWFSk",{"id":255,"title":256,"body":257,"category":276,"date":277,"description":261,"excerpt":118,"extension":119,"image":278,"meta":279,"navigation":122,"path":280,"seo":281,"slug":282,"stem":283,"__hash__":284},"blog_en\u002Fen\u002Fblog\u002Faz-elso-talalkozas-egy-kozos-kuldetes-kezdete.md","The First Meeting — the Start of a Shared Mission",{"type":8,"value":258,"toc":274},[259,262,265,268,271],[16,260,261],{},"On June 3rd, part of the Independent Steps Foundation's (Önálló Léptekért Alapítvány) volunteer social media team finally met in person, while several members joined us online.",[16,263,264],{},"It was a fantastic feeling to sit around a table with people who offer their free time, their expertise, and their energy so that together we can help children living with cerebral palsy (CP) and their families. Everyone arrived with a different background and different experiences, but one thing unites us: we believe that good causes are worth standing behind, and that together we are capable of so much more.",[16,266,267],{},"Even this first meeting was full of ideas, enthusiasm, and a genuine drive to act. I am grateful that such wonderful people have joined us on this journey.",[16,269,270],{},"Special thanks go to the team at Loffice Budapest, who provided the venue for our first meeting. Support like this means a great deal to a foundation just starting out.",[16,272,273],{},"The first meeting is only the beginning.",{"title":110,"searchDepth":111,"depth":111,"links":275},[],"esemenybeszamolo","2026-07-15","\u002Fimages\u002Fpages\u002F01KXJNPK9B5113PRMMZJC0HE61.jpg",{},"\u002Fen\u002Fblog\u002Faz-elso-talalkozas-egy-kozos-kuldetes-kezdete",{"title":256,"description":261},"az-elso-talalkozas-egy-kozos-kuldetes-kezdete","en\u002Fblog\u002Faz-elso-talalkozas-egy-kozos-kuldetes-kezdete","MU1OZoRk-4BNh3hoHg2SdWoQ_s_dIU3sUwlE2mndrSY",[286,581],{"id":287,"title":288,"body":289,"description":293,"excerpt":118,"extension":119,"goal":572,"image":318,"meta":573,"navigation":122,"path":574,"raised":575,"seo":576,"slug":577,"stem":578,"supporters":579,"__hash__":580},"kampanyok_en\u002Fen\u002Fkampanyok\u002Faron-elso-lepesei.md","Help us raise the cost of Áron's surgery and a full year of therapy!",{"type":8,"value":290,"toc":563},[291,294,298,301,304,310,313,319,322,325,328,332,335,338,341,347,352,356,359,362,367,371,374,390,393,397,400,403,406,409,412,417,420,423,426,429,432,435,438,441,444,447,458,461,464,467,470,473,476,479,482,485,491,494,498,501,504,507,510,513,516,519,522,537,540,543,546,549,553,556,559],[16,292,293],{},"Nazarov surgery in Barcelona",[295,296,288],"h1",{"id":297},"help-us-raise-the-cost-of-árons-surgery-and-a-full-year-of-therapy",[16,299,300],{},"He is the little boy who can bring a smile to people's faces even in the hardest moments. He loves being surrounded by people, and he especially treasures the times he gets to spend with his family.",[16,302,303],{},"His family is now working to help Áron sit more easily, stand more safely, and do as many things on his own as possible.",[16,305,306],{},[82,307,309],{"href":308},"\u002Fkampanyok\u002Faron-elso-lepesei#donate","Support Áron",[16,311,312],{},"Every donation brings him closer to moving more freely, doing more things independently, and making the most of the potential within him.",[16,314,315],{},[316,317],"img",{"alt":288,"src":318},"\u002Fimages\u002Fpages\u002FXqBdNPrV6Ptf37QdKc0G7zdfT2spyxPZqnoQXo3k.jpg",[16,320,321],{},"HUF 81,000 \u002F HUF 4,000,000",[16,323,324],{},"2% complete 12 supporters",[16,326,327],{},"Önálló Léptekért Alapítvány",[11,329,331],{"id":330},"we-founded-the-önálló-léptekért-alapítvány-independent-steps-foundation-as-an-affected-family-ourselves","We founded the Önálló Léptekért Alapítvány (Independent Steps Foundation) as an affected family ourselves.",[16,333,334],{},"We know exactly how much strength, perseverance, uncertainty, and hope this journey takes. We know what it is like when every small step forward in a child's development has to be fought for, day after day.",[16,336,337],{},"We work to give real help to children living with cerebral palsy (CP) and their families.",[16,339,340],{},"On this page, we are now raising funds for Áron's surgery and rehabilitation.",[16,342,343],{},[316,344],{"alt":345,"src":346},"Founders","\u002Fimages\u002Fpages\u002Fzeti-team-CuUtw0Ct.jpg",[16,348,349],{},[316,350],{"alt":288,"src":351},"\u002Fimages\u002Fpages\u002FFHBEU3BbvCVsvapxXYSsC0HOUaLKWGROSYOqtE8f.jpg",[11,353,355],{"id":354},"meet-áron","Meet Áron",[16,357,358],{},"If you meet Áron, the first thing you will probably notice is his sparkling eyes and his smile.",[16,360,361],{},"He adores music, nursery rhymes, and all kinds of sounds. Although he does not speak in words, he communicates a great deal. With his gaze, his expressions, and his smile, he can say things that only those closest to him truly understand. His therapists and teachers describe him as a wonderfully lovable, cooperative little boy who is open to the world and seizes every opportunity to grow.",[16,363,364],{},[316,365],{"alt":288,"src":366},"\u002Fimages\u002Fpages\u002FNAO6WgwwAPlTzPxYgnKcWOgC9Nu1SYwvjsAXp0nP.jpg",[11,368,370],{"id":369},"what-are-we-raising-funds-for","What are we raising funds for?",[16,372,373],{},"The Nazarov surgery in Barcelona is a specialized procedure on the connective tissue that helps increase Áron's range of motion, reduce muscle tightness, and support the development of healthier movement patterns.",[375,376,377,381,384,387],"ul",{},[378,379,380],"li",{},"Easier movement — Moving becomes easier for him, and tightness is reduced.",[378,382,383],{},"Better posture — His posture improves, and more favorable patterns can develop.",[378,385,386],{},"Lower risk of contractures — The chance of restricted movements becoming permanently fixed is reduced.",[378,388,389],{},"Room to grow — He gains a new opportunity to develop and move toward independence.",[16,391,392],{},"Alongside this, one of the most important pillars of Áron's development is regular, intensive therapy, which supports his movement, posture, and functional abilities.",[11,394,396],{"id":395},"why-does-it-matter","Why does it matter?",[16,398,399],{},"His journey did not begin easily. At birth, Áron suffered severe oxygen deprivation, which caused permanent brain damage.",[16,401,402],{},"He was later diagnosed with cerebral palsy (CP), epilepsy, and visual impairment. From the very beginning, his everyday life has been filled with developmental sessions, therapies, medical examinations, and countless hours of practice.",[16,404,405],{},"While other children learn to sit, stand, or walk naturally, Áron has to work for a long time for every new movement.",[16,407,408],{},"Sometimes the greatest victory is a steadier sitting position, a more deliberate movement, or a longer moment of eye contact.",[16,410,411],{},"For many years now, the family's life has revolved around developmental work, therapies, and practice.",[16,413,414],{},[316,415],{"alt":288,"src":416},"\u002Fimages\u002Fpages\u002F7XImyWk6gxnLA8ay1sviQwIi3xT0T7OBBUkBXGC8.jpg",[11,418,288],{"id":419},"help-us-raise-the-cost-of-árons-surgery-and-a-full-year-of-therapy-1",[16,421,422],{},"total amount",[16,424,425],{},"HUF 4,000,000",[16,427,428],{},"HUF 81,000 raised",[16,430,431],{},"12",[16,433,434],{},"supporters",[16,436,437],{},"2%",[16,439,440],{},"complete",[16,442,443],{},"3,919,000",[16,445,446],{},"HUF to go",[375,448,449,452,455],{},[378,450,451],{},"The direct cost of the surgery",[378,453,454],{},"Travel and accommodation in Barcelona",[378,456,457],{},"A year-long intensive therapy program",[16,459,460],{},"Every contribution counts. There truly is no such thing as \"too small\" a gift.",[16,462,463],{},"Custom amount",[16,465,466],{},"Optional details",[16,468,469],{},"Donate anonymously",[16,471,472],{},"Donate!",[16,474,475],{},"Secure payment — Stripe · Card payment",[16,477,478],{},"Or transfer directly",[16,480,481],{},"16200010-10145353",[16,483,484],{},"MagNet Bank · Önálló Léptekért Alapítvány",[16,486,487],{},[82,488,490],{"href":489},"\u002Fkampanyok\u002Fzeti","Our previous successful campaign",[16,492,493],{},"Transparent operations",[11,495,497],{"id":496},"transparency-and-trust","Transparency and trust",[16,499,500],{},"Donations are managed by the Önálló Léptekért Alapítvány and are used exclusively for the surgery, treatment, and rehabilitation of the children we support.",[16,502,503],{},"Transparency matters to us, so we report regularly on the progress of the fundraiser and on the children's development.",[16,505,506],{},"Thank you for placing your trust in us.",[16,508,509],{},"Organization registration number",[16,511,512],{},"01-01-0013853",[16,514,515],{},"Tax number",[16,517,518],{},"19425638-1-43",[16,520,521],{},"Documents",[16,523,524,528,529,528,533],{},[82,525,527],{"href":526},"\u002Fpage\u002Falapszabaly","Statutes"," ",[82,530,532],{"href":531},"\u002Fpage\u002Fbeszamolo","Annual report",[82,534,536],{"href":535},"\u002Fpage\u002Faszf","Privacy policy",[16,538,539],{},"Secure data handling",[16,541,542],{},"Court registration: 01-01-0013853",[16,544,545],{},"100% goes to the stated goals",[16,547,548],{},"Regular updates",[11,550,552],{"id":551},"every-step-counts","Every step counts",[16,554,555],{},"These children work hard, struggle, and keep trying every single day. And we believe, unwaveringly, that every small step forward can bring them closer to our shared goal: a life that is as independent and full as possible.",[16,557,558],{},"Thank you for believing in them and supporting them.",[16,560,561],{},[82,562,472],{"href":308},{"title":110,"searchDepth":111,"depth":111,"links":564},[565,566,567,568,569,570,571],{"id":330,"depth":111,"text":331},{"id":354,"depth":111,"text":355},{"id":369,"depth":111,"text":370},{"id":395,"depth":111,"text":396},{"id":419,"depth":111,"text":288},{"id":496,"depth":111,"text":497},{"id":551,"depth":111,"text":552},4000000,{},"\u002Fen\u002Fkampanyok\u002Faron-elso-lepesei",81000,{"title":288,"description":293},"aron-elso-lepesei","en\u002Fkampanyok\u002Faron-elso-lepesei",12,"-SEc7unWsUjbLC-Qzfjz_6xuBijkGhPfpk4P_7GGju4",{"id":582,"title":583,"body":584,"description":588,"excerpt":118,"extension":119,"goal":814,"image":614,"meta":815,"navigation":122,"path":816,"raised":817,"seo":818,"slug":819,"stem":820,"supporters":821,"__hash__":822},"kampanyok_en\u002Fen\u002Fkampanyok\u002Feszti-elso-lepesei.md","Let's help Eszti take her first independent steps!",{"type":8,"value":585,"toc":805},[586,589,592,595,598,601,607,610,615,618,621,623,625,627,630,634,639,641,645,648,651,656,658,660,663,677,680,682,685,688,691,694,699,702,704,707,710,713,716,719,721,724,726,737,739,741,743,745,747,749,751,753,755,759,761,763,765,767,769,771,773,775,777,779,787,789,791,793,795,797,799,801],[16,587,588],{},"Therapies, Borsó Pont",[295,590,583],{"id":591},"lets-help-eszti-take-her-first-independent-steps",[16,593,594],{},"Every day, Eszti wants to prove that she can do it.",[16,596,597],{},"She can put on her shoes by herself. She can put into words what she wants. She can connect with others, play, learn, and become more independent, step by step.",[16,599,600],{},"Every therapy session is another chance to turn those \"someday\" dreams into reality.",[16,602,603],{},[82,604,606],{"href":605},"\u002Fkampanyok\u002Feszti-elso-lepesei#donate","Support Eszti",[16,608,609],{},"Over the coming year, we want to provide Eszti with therapies that support her communication, movement, attention, and independence.",[16,611,612],{},[316,613],{"alt":583,"src":614},"\u002Fimages\u002Fpages\u002FgKTJcmzUl7SgRzOgRinQcQoHi3xKSDs3FrEQDcVU.jpg",[16,616,617],{},"HUF 5,000 \u002F HUF 2,000,000",[16,619,620],{},"0% complete 1 supporter",[11,622,331],{"id":330},[16,624,334],{},[16,626,337],{},[16,628,629],{},"On this page, we are now raising funds for Eszti's therapies and rehabilitation.",[16,631,632],{},[316,633],{"alt":345,"src":346},[16,635,636],{},[316,637],{"alt":583,"src":638},"\u002Fimages\u002Fpages\u002FrSsCxi2gNwndQHZ6z6yl2VuKvy9l5PzaP3GJl3VX.jpg",[16,640,327],{},[11,642,644],{"id":643},"meet-eszti","Meet Eszti",[16,646,647],{},"If you meet Eszti, the first thing you will surely notice is her determination. She is a cheerful, curious, strong-willed little girl who wants to do everything by herself. Once she has made up her mind, it is hard to change it: she is stubborn, independent-minded, and knows exactly what she wants. She will turn down most cakes without a second thought, but she can never resist a slice of chocolate cake — and lately, yogurt has become her absolute favorite.",[16,649,650],{},"Eszti and her mother, Reni, share an especially warm, close bond. Together they celebrate every small success, every new word, every independent movement, and every moment when Eszti takes another step on her own path.",[16,652,653],{},[316,654],{"alt":583,"src":655},"\u002Fimages\u002Fpages\u002F6aEHFLZI9WuDLlrCdUk4DjD3v1E6eucxaM0JsfgK.jpg",[11,657,370],{"id":369},[16,659,609],{},[16,661,662],{},"By supporting her, you are not just funding therapy sessions. You are helping the next steps of a smiling little girl who adores chocolate cake and is determined to become independent.",[375,664,665,668,671,674],{},[378,666,667],{},"Manual therapy — Once a week, 52 sessions in total",[378,669,670],{},"Intensive summer therapies — At the Sher European Rehabilitation Center",[378,672,673],{},"Borsó Pont intensive development sessions — A 4-day program and a one-week intensive therapy in August",[378,675,676],{},"Special education sessions — On a regular basis from September",[16,678,679],{},"And one day, these steps may lead to an even more independent, more confident life.",[11,681,396],{"id":395},[16,683,684],{},"Reni is raising Eszti on her own, and for six years she has worked with all her strength to give her daughter the best possible chances. The cost of these therapies, however, is far beyond what one family can afford.",[16,686,687],{},"Eszti was born in the 30th week of pregnancy by emergency cesarean section due to a severe placental abruption. After birth, she had to be resuscitated, suffered a brain hemorrhage, and later needed a shunt implant. From her very first days, her life has been accompanied by developmental sessions, therapies, and medical examinations.",[16,689,690],{},"Thanks to all of this, she is now a lively, lovable, curious little girl who loves going to preschool and proves every day just how incredibly persistent she is.",[16,692,693],{},"In 2026 she was diagnosed with autism, so supporting her development continues to require regular, intensive therapies.",[16,695,696],{},[316,697],{"alt":583,"src":698},"\u002Fimages\u002Fpages\u002FPqa9HCIOnW39M4JLR1qf0oND7aSPO8FTz287u05B.jpg",[11,700,583],{"id":701},"lets-help-eszti-take-her-first-independent-steps-1",[16,703,422],{},[16,705,706],{},"HUF 2,000,000",[16,708,709],{},"HUF 5,000 raised",[16,711,712],{},"1",[16,714,715],{},"supporter",[16,717,718],{},"0%",[16,720,440],{},[16,722,723],{},"1,995,000",[16,725,446],{},[375,727,728,731,734],{},[378,729,730],{},"a year of therapy",[378,732,733],{},"a year of developmental sessions",[378,735,736],{},"a chance at those first steps",[16,738,460],{},[16,740,463],{},[16,742,466],{},[16,744,469],{},[16,746,472],{},[16,748,475],{},[16,750,478],{},[16,752,481],{},[16,754,484],{},[16,756,757],{},[82,758,490],{"href":489},[16,760,493],{},[11,762,497],{"id":496},[16,764,500],{},[16,766,503],{},[16,768,506],{},[16,770,509],{},[16,772,512],{},[16,774,515],{},[16,776,518],{},[16,778,521],{},[16,780,781,528,783,528,785],{},[82,782,527],{"href":526},[82,784,532],{"href":531},[82,786,536],{"href":535},[16,788,539],{},[16,790,542],{},[16,792,545],{},[16,794,548],{},[11,796,552],{"id":551},[16,798,555],{},[16,800,558],{},[16,802,803],{},[82,804,472],{"href":605},{"title":110,"searchDepth":111,"depth":111,"links":806},[807,808,809,810,811,812,813],{"id":330,"depth":111,"text":331},{"id":643,"depth":111,"text":644},{"id":369,"depth":111,"text":370},{"id":395,"depth":111,"text":396},{"id":701,"depth":111,"text":583},{"id":496,"depth":111,"text":497},{"id":551,"depth":111,"text":552},2000000,{},"\u002Fen\u002Fkampanyok\u002Feszti-elso-lepesei",5000,{"title":583,"description":588},"eszti-elso-lepesei","en\u002Fkampanyok\u002Feszti-elso-lepesei",1,"oAWIadOm_f3fx0cxETUl2P-qeWfr9i5gPtZdnTRVkag",1786466694474]