i think the cheering for sympathizing this award winning offer is available worldwide. and for every language level, learning german has never been simpler. german to go online on facebook, the app store and youtube. the fee is a spinal cord injury and needs working aids. menu was boone with a disability affecting her coordination. paulina has a vision loss and luca and julia have learning disabilities. they tell the stories that move in this edition of detail, we use health magazine,

the estimated spinning of the people in the mood. he lives with disabilities. what makes them not difficult is of nay such them the way they are treated by other people's old society in general. but let's hear from them. i'm in good shape. the people with disabilities sometimes faced outcry, chose tennessee physical assault, insulting junk or remote but other behavior is also been looking. if people with disabilities are continually depicted as victims. when the companions are dressed but not themselves, when health is fullest on them,

even though they never asked for it, or when they are confronted with exaggerated displays of sympathy, as it then lives with less with living. most people with disabilities strongly disagree. whenever sophie holland him dances, she takes her mobility aides with her. she's been partially paralyzed from the waist down since 2017 but that didn't stop the 23 year old from pursuing her dream. a career as a dancer tends to dancing to me is something that comes from deep with it. and in that it's a passion that i live in a language that i can speak for, which i need know, what was it? that's all. she expresses herself on stages across germany. it hasn't been easy to get this far. she had to reinvent ourselves as

a dancer. she began training at a dance academy in dresden when she was 12. 6 years later, doctors discovered a spinal abscess, but an emergency operation came too late. the abscess and partially severed her spinal cord resulting in what's called incomplete paraplegia and leaving her with the question, what now had to and they were not as diagnosed by manifested very blatant avoidance behavior. idle high i said for me in the life i've chosen, it's out of the question that i'll never be able to walk again. i left her alone. never be able to dance again. some time i wanted to be in control of my life, of my body and of deciding what i do is my life is also my labor martha. this determination is evident both on and off the stage when she's not dancing. she enjoys spending time in the countryside near her home and dressed, and she relies on her mental strength and other physical abilities. so if you

holland him refuses to be defined by her disability, begin the disability or characteristics i'm so is being show to me not being able to reach the cup up the or having sensitive skin and needing some fact to 50 rather than 30. that's how it was with me. i just have to learn to cope with my new traits . now also again, and she's successfully carving out a career as a professional dancer. sophie how and him works with choreographer who develops inclusive pieces for dancers with and without disabilities. her goal is to convey the liberating nature of dance regardless of physical limitations. right? found this different, my dream has definitely come true. i live the life of a down. so i guess around, i get to see a lot of cities and to meet great people all the time came down. and so i'm living

the sort of life i wish full not only completely differently than i imagined. i love, but that doesn't make it any worse, especially almost the choreography she's currently rehearsing isn't titled balance. it's about finding your footing over and over again. so if you how and how most certainly found a firm footing in life with downs, the technology is developing a breathtaking pace. some people find that strengthening, they fear losing their jobs. but the advances also provide opportunities. for example, x can age people with vision impairments when they're out shopping or help them to recognize the faces of friends and their expression. artificial intelligence can

open up whole new perspectives. let's take a look at an example from india. b, new money like learning how to use computers and artificial intelligence. a few years ago, she couldn't even hold a pen. the 24 year old from caroline and southern india was born with a physical disability. and i had a lot of problems with my balance. my head was always pulling from one side to the other, completely uncontrollably. i could never keep my balance or sit up straight, things to therapy over to improve it, save my life. that then thing i things to an innovative i t project, a 100 people with physical and mental disabilities now have job prospect new money that it has learned to coordinate the fingers of her right hand. this enables her

to operate the computer keyboard and she's now learning to enter data and create data tags. this data forms the basis for programs that use artificial intelligence . and she'll soon be among those contributing to advances in this new technology. this is, i never thought that i would be able to learn all these things even be able to work and the only industry i just wanted to do my best every day. and then all of a sudden the opportunity came to work here was computers in the that was the move and i realized what i was capable of fled up for the company was founded by robin thomas, who's worked in the industry for many years, for one of his projects, he'd visited the school specifically for people with disabilities. he realized that what they were lacking most were any real prospects for the future. we started giving the whole phenomenon what we have to create an ecosystem for them to bring

this change, sustain the scene and bring us us. so i forgot to call me behind it. so that's the, that's why you were committed to do that because we cannot give them just some technology getting degree thing, the technology back to the society. we're bringing people together and save us that goal system so that everyone can contribute to that. it was the foundation is late here at the therapy center here in the new money lot is working on her motor skills. the focus is mainly on her strong hand, the right one. because this training method takes the form of a game, it distracts or a bed from the pain. she experiences doing the exercise that busy then and then i only improve when i train constantly. at 1st i cried in the in the thing that now i'm so happy about my progress, i almost don't care about the pain any move in the to the robin

tommy is overjoyed to see the strides made by the children and young adults. here. he succeeded in attracting numerous companies as donors and cooperation partners. the money is mainly invested in new technology for any special education, so your name and he goes to the a basic gave me fight that the system do you think is a lot of insight on the therapist. so what needs to be taken care whether it's his upper body? no valve, body goose motor, a fine motor. the motor of that kind of milestones will be defined, mino, moneys. i also studies at home for her new job in her room. she often spends hours, practicing computer commands and english vocabulary meanings, and that's the discipline grammar. the news, the other bins say they get now and she says, all that effort is paying off feeling valued like this is a great incentive for her to keep going with the,

the good. i managed to listen to gross things, but we can look at the beginning. i thought it was impossible, but we have time to go better and better. and now i'm being trained in the i t sick, so that's something else i would have to complete. again, go beyond her pain threshold and have to overcome numerous hurdles. and she's already learned a valuable lesson to never underestimate her own abilities. every 5 seconds, somebody in the of experiences vision loss. 9 out of 10 of those who are affected live in low middle income countries. inadequate health care or mail nutrition, often to blame vision. those can result in a vicious circle without schooling, training or job. many of those effected condemned to life in poverty. and we'll see

countries the situation is less extreme, but there's too much to do. germany's national organization for people with visual impairments, for instance, has highlighted the danger electric calls pulse because they to client they might be many more problems elsewhere in the world. but it shows how the needs of people with disabilities often get a window of time to raise awareness. usually you use a mirror to put on makeup, but pouting a kreger, a severe vision loss. she had to re learn the process by feel cutting last move, i can only see 0.01 percent is that if you can even tell me when i could still see something, i like to do my makeup since becoming blind. i've learned what movements to make you. i've trained myself to do it on happiness. i thought i'm putting it. it's all a matter of practice, but it's still good to have a sista ungainly cub checking. is that okay?

or a but high up on the social media optic talk the 19 year old shift to everyday life with the whole world, a human. so 1st, imagine you're blind, the person comes up to you and tells you you're putting, what will you do then? of course, at the beginning you say thank you, talk to them, then you say you are too low. so what should i do? i've done that on the phone. i started doing it back in 2020, just for fun because many people have written to me asking me how i cope them, how i can be blind, and yet not quote unquote, sofa items and food solution. the system has and i found i can motivate people with my videos and make them laugh and to some of them going to show clips, get a lot of clicks. one video, you can go type a 1000000 that her mother was a bunch of the joke. you've had moved them out. she was begging of the cars and she

awesome. mm hm. is anyone behind us and then the thing and everyone was like, well, is she forgot my lines just sleeping issues and i just played along with the opposite. no, mom my best. no one is all clear called to us out, then stopped and just started laughing. marina nichol can handle it. the mother and daughter were being through a lot together, numerous doctors visits and treatments. some of them abroad, like the one in cuba, the 12 and it was also a very stressful, scary what was happening. love us proceeds versus adult trip. cool. shed those fears. i'm worried about sharon future to kind of you all right. i called to buy con book. i won't get a boyfriend. i'm not going to have children and stuff like that. yeah, i'm a piss me. so i also wondered why i got this disease and not my siblings or someone else. i'm because that probably in a nickel has come to accept things. well,

it's more she's married and is about to have a baby. she's had a lot of practice often looking after her little sister. you have them with us. i saw what was involved to come have i have helped out a lot. so i said to myself, it looks as if i can also change diapers despite vision loss and new challenges are on the horizon. and no doubt new stories for take talk to the people with vision loss often seem to have other enhanced sensory skills. for example, they might be able to share how far away your call is or feel when a subway train is approaching. sometimes what is regarded as an invitation can give rise to read and special skills working send to meet or by centimeter. her hands can detect life threatening changes early jennifer gordon's extraordinary dexterity allows her to feel very small changes in breast tissue. she

has almost complete vision loss. that's why she's a medical tactile examiner or m t u for short as well. i have some beats here and they represent a we compile page lumps the smallest hoff a send to me to the next 2 or what the doctor is able to pay. and that's one sense metering size up woods when he left the last 2 or what a patient can feel to send to meet his upward sites. and that can already be far too late. and jennifer has a hereditary disease that causes complete loss of sight. when she was diagnosed in 2015, her world came crashing down. all of us come out of it. i asked myself, what kind of visually impaired person do? then discovering homes came along, i was just blown away such a relief and so beautiful a function of the organization, discovering hand strains visually impaired women under medical supervision. they learned to carry out breast examinations with

a kind of mapping system. so no areas are missed. ready getting these, these fi, sticky strips for my orientation, so i can scan them to press row by row, send to me to by send to meet the end 3 debt post and come the procedure last between 45 and 60 minutes and includes the lymph nodes. jennifer bolton's sense as any irregularities. what medical tactile examiners do is not a substitute for mammograms, but it does offer gynecologist a valuable additional tool. dr. andre multimedia from hamburg immediately decided to offer the service and his practice as gets why it is they are going to aspect on this project has 2 very good aspects of this. one is the improvement in preventive care for him into a supplementary examination at regular intervals, sometimes detect something that would otherwise not have been seen until a year later during a mammogram. does this tony? and the 2nd is that it's great. of course that visually impaired women can do

a very meaningful job and maybe feel more accepted in society then if they couldn't do it. could like jennifer, blue and see was found a vocation because of her exceptional sense of touch assistant and gets a chance has the profession that tons of disability into a gift. i can now work until retirement. i think it's great. i have really great patients. a great problems with my patients as well as with the doctors. it's wonderful. there's nothing that i dislike about it next to the fender and the patient's no. with jennifer boons. they're in the best of hands, a down syndrome, medically known as tries to me. 21 is not an illness, but a genetic condition. sometimes people with down syndrome get lumped together and all too often they get treated like children. they've all states and traits

commonly associated with the disorder. but people with down syndrome are as unique as everyone else. with different intellectual, artistic and practical affinities, as interests they can fall in love, live independently and also do a really good job. julie is working day in a bed and breakfast starts at 7 am, the breakfast he meets that with manager back. so in the kitchen to be allocated the toss the day, the i fill out the time sheet, then it makes breakfast to the rooms and bathrooms. if julia provides to work behind the scenes, she's shy of being with a lot of people make so nervous. a challenge and this job. lucre enjoys customer

contacts and working in hospitality. he likes trusting with a guest and telling them about the work here. people with disabilities to everything here. the team is now complete and best to tell them again what needs to be done. they have 2 rooms to clean and beds to make julia and gabriella, take care of the 1st room. it's important. nobody puts them under pressure. the, the combined, the, my co worker, julia headed monte is very session evans of a guy eh, no, but i know she doesn't talk much a lot. but i want to say, i liked this work a lot. it just, i'm proud to be working. and my work is very important because i bring home a salary and help my family as a i,

i mean for me. yeah. that's the distinctive thing about this project. this small hotel, cold to low races is not publicly funded. it's a business that needs to turn a profit. its employees have to train and go through an application process, then they get to put them in and contract. the cookie trailed the middle top. everyone earned their contract to the all 4 of us really worked for him a bit more when we made some mistakes to of course, but younger, i think this idea should be implemented across satellite and also be adopted in other countries. or the voted meals by the driving force behind the project. judy, as parents, they formed a cooperative purchase. this property neither had any prior experience in the hotel business, but they were determined to set up something for julia and others. almost as if we wanted people to understand that these young people can work well. everything here

is tailored to them, but the idea would also work and other to assess ability and re co pay. demonte also has other plans. next he wants to open a pastry shop, the offers gluten free products. no. because many people with down syndrome inclusion, intolerance, or quality, a table, a k. the goal is to create a permanent training facility here to train many people with down syndrome and then facilitate the integration of these young people into other jobs. i mean, some of the opposite, opposed to the level. judy is working day is over. i'm going dancing now, but i'll be back at work again tomorrow. the only a small percentage of people that go on with disabilities. 90 percent occur later in life as a result of serious accidents or illnesses like meningitis, osteo,

my nitrous oh polio. cancer can also be life changing. steven lifetime last part of his leg 12 years ago of can stand on one leg just fine. he was just 17 when he was diagnosed with bone cancer. after a year with chemo therapy, the tumor was removed along with his knee joint and got a new replacement. the worst was to come. can you get in cottage of purple bush? the neat joint often got bent out of shape or various move montage dvd, im gonna titanium rods, and the bone came loose rather than fusing with it. that leg became shorter. what occurred with time and my movement was affected. they had got harder to walk down stairs and went off. in the end, i only had around 30 percent move election and i often got stuck in mid movement

and fell down the stairs. as a result, i entered my real new cap and the last 5 each. i have a fillets and all steven lines that i had to undergo more than 40 operations. during one of them, the wound crew infected and the antibiotics didn't help. he made a life changing decision, this henry started location. it was also upsetting. i realized that then i could live with the decision to have my leg removed. but since i was the 1st that meant i wouldn't be in pain anymore. secondly, that i'd be rid of the whole thing and the infection too, and often and see if i woke up in intensive care. and the 1st thing i did was pull back the covers helpful. and i looked down and saw it was finally gone. i was happy i was really happy in and i had tears in my eyes. stephen struggling through his hospital stay in subsequent physical therapy and gradually grew accustomed to life with a prosthetic leg process that lasted several years. let's find out. it

took a long time, the operation was 11 or 12 years ago, but i only finally managed to get the right fit for years ago. which div, that's how long it took to get it right. before that is that the shaft didn't fit, the prosthesis broke, or it had to be readjusted. the sometimes i was in the medical supply store 3 or 4 times a week. i'm off the 42 year old tries to live a completely normal life. never the less certain routines have become 2nd nature. the 1st thing he does in the morning is go to the bathroom to put on his prosthesis . stephen is passionate about his blog, my leg and me. he's active on youtube and instagram. to find internet truck. obviously in my blog, i reveal my emotional state. if i'm going to, i want to share with the world what i've been through, what my problems are, is best mine. and hopefully i'm is maybe someone has the same problem and can reach

out kind of, there are some people who are effective, who have problems which i need to go through, we're about to have an amputation. and we simply ask, interesting, how does it work? and as far as what happens, you know, it's just, i'm thinking, what do you have to take into accounts? are there any problems? where can i get a little help and visual claim? uh and then i try as best i can to answer their questions when i'm done for those things of what he's good to find because i'm to bon talking and he also meets many of those effected in person the mesh duncan lloyd 9. so i just want to help other people find their own way so they can be as happy again with their lives as i am stephen has been married to on. yeah. for 13 years. documents comforted because she's been with me through the whole story from the outset to the amputation. she accepted me even without my lack of this. it was no problem for her to me. she said the main thing was that i'm happy and pain free

as now. a long struggle that's ended well for stephen, he loves his wife and wants to continue showing that to the world the. that's it for today. see you next time on in good shape, by the

a beautiful life event. how to make it unforgettable. germany has to be seen special wedding traditions, but what are they? honda who most finds out your womack or 30 minutes on marriage is forever. the horse is forbidden

in the philippines than what god has joined together. no man should ever tear apart . even if that man abandoned his family a long ago. so far, all major reforms have failed with something in the society. his mindset is changing for us in 75 minutes, dw, the every day counts for us, for our planet. the ideas is on its way to bring you more conservation. how do we make ceilings green or how can we protect habits? with all our waves?

we can make a difference by choosing smartness solutions, overstaying, set in our ways. global ideas, environmental series included, $3000.00 runs the loudest voice. i am must the new jobs. she's the face of a protest movement. i didn't think so many women would send me the photos. she's there motivator. all of us hire a little must be the and she won't give up to watch the assignment for public took my brother hostage a few days ago. but at the trying to sign in the see as a new job, they won't be silent. starts june 3rd on dw,

the business think they'll be used to live from the lien. red chip type o one wins. and now the 5 used as president of turkey. after receiving 52 percent of the bodies in the runoff election, or the one until jubilant. supposed is that turkish units he will be present with you for about corresponding outside the presidential palace.