본 영상은 세이브더칠드런과의 협업으로 제작되었습니다. - 세이브더칠드런은 전 세계 모든 아동이 건강하게 자라고 위험한 환경으로부터 보호받으며 교육받을 수 있도록 지원합니다. [세이브더칠드런 발달장애아동 참여 가이드라인 바로가기] 다운로드: www.sc.or.kr/news/reportView.do?NO=71667 [세이브더칠드런 온라인 아동권리교육 바로가기] 온라인 교육 사이트: e-learning.sc.or.kr/userMain/goUserMain?lang=ko ▶아동권리 기본교육, 아동안전보호 정책교육, 반차별 이해 교육, 긍정적으로 아이키우기(기본교육)
it makes me reflect on myself to see that child with down syndrome also say that she will try shes best. from now on, i will be grateful for the present life.
I have a sibling with Down syndrome and this made me cry because I know that anxiety and fear of us he able to do it alone, will he do it right if we let him do it alone
I'm so proud of her.. Her mother is doing great not only for her daughter but also making society aware and helping in social inclusion. The writers and directors of ODG should be applauded for being a part of this :)
7:35 I love the confidence she said that with. She knows her daughter is capable, and that she will be there helping her work on that, and in any obstacle she faces until Jimin can do it on her own. What a great Mother. My nephew has Down Syndrome, so this was even more touching. I loved watching this story and get to know Jimin.
Me too, but I wonder why they don't have walking groups like in Japan, where the sixth graders in the neighborhood lead everyone else to and from school. Seems safer for everyone.
This made me tear up. So proud of Ji min. She wasn't nervous at all and she was enjoying her journey alone. I'm also so proud of her mom for letting Ji Min go to school on her own and let people know that Ji Min is special, it somehow educates other people that kids/people with special need are just like us but with special traits. Ji min, fighting!
As someone who is autistic, most autistic and disabled people do *not* like the infantilizing euphemism special needs, this from neurodivergent_lou explains it better: "Disabled people's needs are not special, extra, burdensome or additional, they are human needs. Referring to disabled people as having special needs is inaccurate. As an autistic person, I need to be able to communicate and express myself, that need to communicate is not special, that need is the same as every non disabled person. I might just need accommodations in order to communicate. The term 'special needs' makes it feel like accommodating disabled people is optional, which it is not. The term special needs is also associated with special treatment too and it gives society the impression that instead of accessibility being a right, it is 'special treatment' or a 'special privilege.' If disabled people's rights were seen as the rights that they are (instead of being seen as extra, additional or special) then perhaps wheelchair ramps would be in every building, plastic straws would be available to those who need them and disabled toilets would be made to be available and accessible. Instead, disabled people's accessibility rights are seen as an afterthought. I want to see disabled people's accommodation needs normalised and the term special needs does not do this for me. It 'others' disabled people. It separates disabled people's needs and the needs of non disabled people. When I was labelled as having special needs as a child, it took away my ability to feel pride in my disability too and see disability as part of my identity. The term special needs often infantilises disabled people too. Disability is not special, rare, exceptional or unusual. Disability is a normal part of life. The term special needs makes it sound as if it is unusual or rare. This too heightens the inaccessibility cycle. If people believe that disabled people are few and far between then people don't see the point or the benefit in accessibility. Accessibility is however vital. Sometimes people say that they don't see my disability but just see my needs, specifically my 'special or additional needs.' I feel that this is often because people see my disabled identity as something inherently negative, which I guess is part of growing up in a society which sees disability as something to be ashamed of. I need people to recognise my disability. I am exhausted by the euphemistic terms used to describe disability. which I guess is part of growing up in a society which sees disability as something to be ashamed of. I need people to recognise my disability. I am exhausted by the euphemistic terms used to describe disability"
@@aussiefurbymogwaifan6621 yes :) but I also throughly enjoy watching kdrama/movies also which also use the phrase "fighting" a lot. It's a widely used phrase both by actors/actresses and idols to send encouragement to their fans as well as their colleagues and vice versa.
@@aussiefurbymogwaifan6621 As someone who is also Autistic and has many other disabilities/conditions/chronic illnesses I absolutely LOVE this and completely agree with every single word!! 🥺💜 I'd also like to add that I also absolutely hate it when people kind of just lump all disabilities/conditions together and think that we're all the same and need the same accommodations or the same level of support or are at the same mental age etc when that's really not the case at all like we're all different and we need different things! It especially happens with Autism though like most people don't seem to realize that Autism is literally a whole entire SPECTRUM, like I used to be on this college 'course' thing (it wasn't really a course, it was just where the college decided to throw everyone with disabilities/conditions/social issues etc because they cba to actually properly help/support us) and even though we all had different disabilities or where at completely different levels/mental ages they still just decided to treat us all the same! We were split into two groups which was 'The Independents' aka people like me who can still look after themselves and be independent and were mentally are physical age and then there was the 'non independents' which were the people who had severe disabilities and couldn't look after themselves or be independent etc and even though we had those two groups, they STILL treated us all the same anyway and gave us all the same level of support/accommodations which just didn't work at all like us 'Independents' where literally treated and talked to like little brainless toddlers which was extremely humiliating and degrading! Like they just didn't seem to realize that we weren't all the same and that we all had different kinds of needs that needed different kinds of support/accommodations or that us Autistic people were actually all on different parts of the spectrum etc and it was extremely frustrating and i'd honestly never felt so depressed before in my life while I was there like it legit felt like a prison 😅🤦♀️
안녕하세요 지민이와 같은 초를 다니고 있는 다른학년 언니입니다.지민이가 학예 발표회를 하는 모습을 직접 봤었어요 그때 다른 아이들과 다름없이 끝까지 잘 참여하고 열심히 하는 모습을 보고 대단하고 존경한다는 느낌이 들었습니다.지민이는 영상으로도 실제로도 정말 긍정적인 아이처럼 보입니다.앞으로도 지민이가 혼자 학교를 조심히 다닐수 있는날을 기다리겠습니다:)
다운증후군인 저희 오빠는 이제 32살이 되었습니다. 초등학교2학년때까지만 해도 제가 같이 등교하고 급식시간에 밥 대신 받아주고 했었는데 이제는 사회적기업이긴하지만 혼자 출퇴근도 하는 성인이 되었습니다. 저희 부모님 마인드가 지민이 어머님 마인드랑 비슷하세요. 중학교까지 일반학교를 나왔는데 등교할때 버스도 타고 걸어도 가야하는 등교길을 중학교때 처음 혼자 가도록 시켰었어요. 부모님이 변장하고 버스 따라타고 학교도착할때까지 미행아닌 미행도 하고 그랬었네요. 그런데그런 불안한 가족들의 마음에 확신이라도 주듯, 오빠는 한번도 길을 이탈한 적없이 등교 잘했어요. 그 이후로도 한 두번만 같이 가주면 혼자서 버스도 잘 타고 길도 잘 찾아가요. 이제는 퇴근길 지치면 가르쳐준 노선도 말고 빙 돌아오는 노선을 스스로 어째 알고 바람도 쐬고 돌아올 줄 아는 성인이 되었어요. 저희오빠는 지민이처럼 의사표현도 정확하게 하지 못해요. 그래서 길을 잃었다는 표현도 못할까봐 걱정을 많이 했는데 오빠는 항상 저희의 기대 이상이었어요. 그래서 저희 가족은 더 오빠를 믿어주고 도전을 응원했습니다. 중간에 아찔한 경험도 많았지만,, 감사하게도 시민분들이 도움도 많이 주셨구요 ㅎㅎ 지민이 어머님도 지금처럼 옆에서 항상 지민이 응원해주시면 지민이도 어머님 불안하게는 안할거예요. 장애아동의 부모로 산다는것이 마음졸이는 일도 고민거리도 많다는 것을 부모님보고 어느정도는 알아요. 지민이 어머님 지치지 않으시길 무너지지 않으시길 그리고 지민이 건강하게 잘 성장시키시길 항상 응원하겠습니다! 그리고 발레수업을 통해 같이 성장하는 친구들에게 장애인과 비장애인의 공존을 느끼게 하시는 것도 정말 대단하세요👍 지민이 언제어디서나 주눅들지 말고 건강하게 자라요~ 응원할게요❤
나는 이것이 잘 번역되기를 바랍니다. ASD(자폐증 스펙트럼 장애)가 있습니다. 하지만, 아는 사람은 많지 않습니다. 너무 기뻐서 울고 있어요. 지민이 해냈어! 축하합니다! 그녀는 정말 잘했고 당신은 내가 아는 최고의 어머니 중 한 명인 환상적인 어머니입니다! 행복하고 건강하세요. 새해 복 많이 받으세요!
This was so emotional for me. My sister (who was born in 1973) had Downs Syndrome. She was 7 years younger than me and I had the responsibility of taking care of her. She was my baby and I loved her so much. She was also raised to be independent, and accomplished so many things during her lifetime, so much to say it was very full and happy. She even traveled the world with my parents. She passed several years ago from severe pulmonary embolism. I don't think the pain of her loss will ever lessen. She will always be my angel.
초등학교에서 일하는 특수교사입니다. 지민이 보는데 같이 마음이 조마조마하고 대견해서 코 끝이 찡하네요. 수업 끝나고 통합반으로 우리반 아이 혼자 처음 올려보내던 날, 몰래 아이 뒤 따라가면서 혼자 잘 갈까 지켜보았던 때가 생각나요. 이제는 혼자서도 곧잘 반으로 올라가는 아이들이 얼마나 대견한지 몰라요. 우리반 아이들이 보고싶어집니다 ㅎㅎ 지민이의 앞날을 응원합니다 !!❤
I am working in a school of children with special needs, and I swear they are the sweetest ever. That little smiles everyday helps me to be positive everyday. Well done Jimin. You did great💜💙
Props to the camera guy! When Jimin got distracted, he helped her re-focus but in the most respectful way and while still giving her autonomy! He just said “let’s go” and then follows Jimin as she leads the way again ❤
As a mother of an autistic boy, I completely understand when she says we don't wish for much. Just that they are healthy and accepted by society. They are perfect just the way they are 🥲 What an amazing daughter and mother 💚
횡단보도 둘러보는거 ㅋㅋㅋ 너무귀여워여 ㅋㅋㅋ 어머니 사랑이 느껴지는게.. 정말 가슴이 따긋해지네요... 귀여워서 웃다가, 어머니 사랑 느껴져서 눈물도 나고.. 어머니의 인터뷰는 현명함과 강함이 느껴져요. 지민이가 씩씩한 이유는 든든한 가족 덕분이네요.. 대단하십니다!!
It’s so beautiful that the only real importance to mom is that Ji Min is HEALTHY. It’s scary letting your children out into the world regardless of the situation and mom is doing an amazing job of fostering inclusivity and awareness. Beautiful family, beautiful Ji Min. FIGHTING!
장애전문기관에서 일하는 사람의 입장에서 보는데도 어머니 너무 대단하신것 같습니다. 요새는 장애 비장애 상관없이 부모님, 보호자가 너무 다 해주는게 많은데 그런거없이 당당하게 키우시는 모습이 너무 대단하다고 생각을 했구요, 어머니의 ”이러면 평생 아무것도 못할것 같다“라는 말에 정말 공감을 하고 봤네요. 그리고 지민이 너무 똑똑해서 나중에 커서도 사회생활 잘 할 수 있을거같애요! 말도 너무 잘하구요 표현도 너무 잘 하는 모습이 대단합니다 정말!!❤ 지민아!! 나중에라도 이 댓글을 보게된다면 꼭 예쁘고 건강하게 자라자❤❤❤
어머니의 모습에 걱정과 떨림이 공존하지만 제 눈엔 설레는 모습으로 비춰졌어요. 더불어 모든 인터뷰의 한마디 한마디가 멋진 분이라는 생각이 들고요. 새로운 도전과 세상을 향해 한 발 더 딛는 지민이를 응원합니다. 더불어 피곤한 아침 행복한 눈물 한방울 흘립니다. 오디지 감사합니다
Very proud of both Jimin and her mother. It can be scary to let a child do something like alone for the first time whether they have down syndrome or not. Jimin did great and her mother was very confident and strong in her belief in her child.
저희 언니가 다운증후군인데 엄마와 언니를 보고 있는것.같아서 눈물이 살짝 .. 났어요 😢 혼자 버스타는법, 장보는법 ,간단한 음식하는법등 생활할때 필요한 모든걸 가족이 반복적으로 가르쳐서 일상생활에 불편함이 없도록 했거든요.. 지민이가 혼자 학교로 씩씩하게 걸어가는 모습이 너무 기특했어요. 어머님이 너무 훌륭하신것같아요 ! 응원합니다 ❣️
코로나 전까지 정확히는 2020년 4월까지 지민이를 자주 봤던 사람으로서 지민이가 이렇게 건강하고 밝고 씩씩하게 자란 모습을 보니 감탄과 감격으로 가슴이 벅찹니다. 지민이 어머니도 넘넘 반가워요. 맑고 맑은 지민이가 제 볼에 뽀뽀해 주고 나면 그 날의 피로가 풀렸던 따뜻했던 기억이 납니다. 지민이가 앞으로도 행복하기를 혹시라도 고비가 생긴다면 씩씩하게 타 넘고 다시 행복해지기를 기도합니다.
다운증후군을 안고 태어난 아이를 둔 부모로서 이런 모습을 보니 기쁘기도 하고 가슴이 아프기도 했습니다. 이 아이들은 다른 사람들처럼 대접받을 자격이 있는 순수한 천사이지만, 스스로 학교에 걸어가는 것과 같은 성취도 인정받아야 합니다. 이 비디오를 만들고 공유해 주셔서 감사합니다.
지민아~~~ 같은 초등학교 (12년 전에 ㅋㅋ) 졸업한 언니야 ! 내가 오래 전 졸업한 학교에 다닌다니 너무 반가워서 댓글 달아 ! 학교에서 선생님들과 친구들과 좋은 추억 많이 만들기 바라🥰 혼자 등교하는 모습이 참 씩씩하다. 어머님이 당부하신 말씀도 잘 기억하고 길 건너고 ! 대견해 ! 언니는 발달장애를 가진 사람들이랑 함께 시간 보내고 있는데, 사람마다 다 성격이 다르고 각기 다른 특징을 갖고 있듯이 많은 사람들이 장애를 특별하게 구별하지 않고 하나의 특징으로 보면 좋겠다는 생각을 하곤 해 앞으로 건강하게 지내길 멀리서 응원할게 지민아😍😍
어머니 정말 현명하고 단단하신분이시네요... 애기도 없고 장애를 가진 지인도 없지만 반성하게됩니다.. 아마 지민이는 어머니를 닮아 현명하고 건강한 어른이 될거에요:) 응원하겠습니다! 지금은 혼자 400m의 등교길을 걸어갔지만 이후에는 400km떨어진 곳에 여행도 갈 수 있을정도로 단단한 지민이가 되길!! 지민이화이팅🫶🏻
I have a sister with Down’s Syndrome. As young kids I just knew it took her longer to learn certain things. Basically my attitude was if I have to do it so do you.😂 Happy to say she graduated from high school two years after I did and she now lives in an apartment and has a job. She’s doing great! Doctors said she would not learn to read but because I didn’t know any better I made her and she does a great job! She’s extremely sweet, kind and capable and I am so proud of her. Ji-Min reminds me of my sister.😊 Even the heart surgery for the hole. Fighting Ji-Min!
As a person working on a field towards helping kids with special needs, Im so happy that this channel is promoting inclusivity!!! Also so proud of both jimin and her mother! They’re both doing a really great job! 💜💜
As someone who is autistic, most of the disabled community dislike euphemisms like "special needs", this from neurodivergent_lou explains more: "Disabled people's needs are not special, extra, burdensome or additional, they are human needs. Referring to disabled people as having special needs is inaccurate. As an autistic person, I need to be able to communicate and express myself, that need to communicate is not special, that need is the same as every non disabled person. I might just need accommodations in order to communicate. The term 'special needs' makes it feel like accommodating disabled people is optional, which it is not. The term special needs is also associated with special treatment too and it gives society the impression that instead of accessibility being a right, it is 'special treatment' or a 'special privilege.' If disabled people's rights were seen as the rights that they are (instead of being seen as extra, additional or special) then perhaps wheelchair ramps would be in every building, plastic straws would be available to those who need them and disabled toilets would be made to be available and accessible. Instead, disabled people's accessibility rights are seen as an afterthought. I want to see disabled people's accommodation needs normalised and the term special needs does not do this for me. It 'others' disabled people. It separates disabled people's needs and the needs of non disabled people. When I was labelled as having special needs as a child, it took away my ability to feel pride in my disability too and see disability as part of my identity. The term special needs often infantilises disabled people too. Disability is not special, rare, exceptional or unusual. Disability is a normal part of life. The term special needs makes it sound as if it is unusual or rare. This too heightens the inaccessibility cycle. If people believe that disabled people are few and far between then people don't see the point or the benefit in accessibility. Accessibility is however vital. Sometimes people say that they don't see my disability but just see my needs, specifically my 'special or additional needs.' I feel that this is often because people see my disabled identity as something inherently negative, which I guess is part of growing up in a society which sees disability as something to be ashamed of. I need people to recognise my disability. I am exhausted by the euphemistic terms used to describe disability. which I guess is part of growing up in a society which sees disability as something to be ashamed of. I need people to recognise my disability. I am exhausted by the euphemistic terms used to describe disability"
I dont even know her but feeling so proud when she succesfully reach her school on herself. Waving to the camera and look how happy she is when she did it, stomp her feet and her shouted "Great!" Wish i can have a nice mood when i goto school like her. Also want to appricate her parent is mindset and effort on trying to changes the society is perspective to be more inclusive . (sorry for my bad english)
Her mother watch her on the window. J min make it arrive school . That’s great ! . She smart girl . Her mother happy for her . That’s sweet . God bless to her .
자폐스펙트럼/발달장애를 가진 아동들을 치료하고 있습니다. 아이가 너무 대견하네요.. 어머님이 얼마나 노력하셨을지 제가 다 눈물이 납니다ㅜㅜ 어쩜 혼자서 등교를.. 계속해서 자신이 오고가고 했던 길을 기억해내고 쉽지 않은건데 지민이 또한 엄마의 가르침에 열심히 임한 것 같아서 감동적이에요 세이브더칠드런 2019년 12월부터 후원하는 중인데 제가 좋아하는 채널과 협업해서 홍보영상도 찍고 앞으로도 긍정적인 영향을 펼치는 채널이 됐으면 응원합니다 ㅎㅎ
사람은 누구나 장애가 있어요. 다수가 가지고 있는 장애인지 아닌지의 차이가 있을 뿐. 지민 양은 잘 할 겁니다. 세상은 누구에게나 지켜주는 이가 많을수록 아름다워집니다. 진정으로 더불어 사는 세상이 되어 서로가 서로를 지켜줘가면서 살아갔으면 하네요. 지민 양 건강하고 또 건강하길 바랍니다.
저도 발달장애인의 가족이자 발달장애 아이들을 가르치는 선생님입니다. 혼자 학교가는것이 누구에게는 별 것도 아닌 일이지만 지민이가 이렇게까지 해낼 수 있도록 부모님과 여러 주변의 사람들이 도와주고 가르치는 시간들이 얼마나 쉽지않았을까 생각되네요. 이런 영상 하나가 정말 어울려 살아갈 수 있는 좋은 영양분이 될 거라 믿습니다. 항상 건강하시고 응원합니다❤
Ji-min did a very good job, she got distracted a few times but then she was right back to getting to where she needed to go. Her mother is so supportive and sweet I hope she knows she’s an amazing mother❤ she’s going to have great success
Ain’t gonna lie, I teared up for the mom. Down syndrome or not, I’m a mother and I would still watch my kids from a distance. It might be 2023 but this world still fucked up. Just sayin’ It’s ALWAYS kids safety. She’s brave and beautiful! I love her 🫶🏽 YOU TOO, MOM. 🙏
