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  • I'm Yuriko Oda and my disease is distal myopathy

  • HIBM / DMRV / GNE Myopathy

  • When I was 20 years old I feel some abnormal change with my legs.

  • And when I was 22 years old I was diagnosed with distal myopathy.

  • When I was 26 years old

  • I began to use wheelchair because I couldn't walk as usual.

  • And I had baby, so I and my husband and my baby go outside together.

  • My name is Josh Grisdale and I'm from Canada,

  • near Toronto originally, and I've lived in Japan for about eight years now.

  • I have what's called cerebral palsy and it means that i had brain damage when I was a kid.

  • It might have been a high fever I had when I was about six weeks old.

  • So after that it effected my arms and my legs so i can't move them as I intend to.

  • And communication between my brain and my body is the problem.

  • My name is Minekazu Tsuchiya.

  • I'm an office manager at STEP Edogawa.

  • I was in a motor bike accident 28 years ago.

  • Since then I lived with my parents and went to the hospital.

  • I moved to Tokyo 12 years ago.

  • Medical care and helper, Japanese government pay for us and

  • we pay around 10 percent, it depends on their salary

  • To add to what Yuriko is saying, there's a cap on the monthly amount you'd pay.

  • Additionally, if you're low income, you'd pay less than someone with a higher one

  • I say a benefit for me in the way that the system is set up

  • is that it's not necessarily distributed by the country,

  • as much as the through the city.

  • So if you're living in a city and you're registered with the city

  • and you pay your city taxes then you're eligible to receive the city services.

  • And so that's who's in charge of sort of dispensing the helper time.

  • And some of those accessibility services and stuff so...

  • Even though I'm not a Japanese citizen I'm still able to

  • receive those things as a citizen, or, a resident of my city.

  • So it's more residence then nationality.

  • And it can change depending on which city you live in as well.

  • So if i move to a different city then I'd obviously fall under that city's situation.

  • So that could change what services i receive and stuff so...

  • We get assistant services for people with disabilities.

  • It is different from the Long-term Care Insurance for the elderly.

  • Part of the assistant service is a home helper service where a helper visits you at home.

  • There are helper services that aid in going out or going to a hospital and so on, which are subsidized by the government.

  • The hours you receive depend on how severe your disability is.

  • Depending on how bad your disability is and your condition, your benefits will change.

  • It's really complicated to explain, but to easily say it, there are different levels.

  • I get home care service for people with severe disabilities, which is pretty much the maximum support you can get.

  • In order to get my benefits I applied to the Edogawa ward (city) office.

  • Then the Edogawa ward office reviewed my application and decided how much benefits I would get.

  • I get a 302 hours of home helper service a month.

  • My name is Shoichi Adachi. I'm a helper.

  • While the disabled people I met could do many things on their own,

  • they all required aid from helpers.

  • I shouldn't open your closet, should I? Right, I won't!

  • Ah, could you microwave it for about 1 minute, please?

  • Thank you so much.

  • Ahhh, Sooo good!

  • I'm really careful when I work with a person whose values aren't the same as mine.

  • I try to think as if I were that person, putting my values aside.

  • I'm here to support my client's life, so that's what I focus on.

  • I always remember I'm just here to help my client.

  • By myself I can type and I can handle a ride in my wheelchair

  • and brush my teeth with an electric toothbrush.

  • Other activities I cannot do by myself.

  • When I travel I (go) with (my) husband.

  • But in my house I ask some helper

  • to help wash dishes or laundry or clean my house.

  • The three main types of help that i saw provided

  • were for physical needs like assistance going to the washroom or getting dressed.

  • Daily life needs like cooking food and cleaning.

  • And social well-being needs

  • like traveling outside of the home to interact with others and the world.

  • I asked how the help was provided and it turns out it depends on the individual

  • and the company providing the support.

  • Since every individual's needs differed so did the support they received.

  • I plan my helper tasks on a weekly basis.

  • My helper comes in the morning to help me get out of bed, go to the bathroom, and change my clothes.

  • Then there's lunch time, dinner time,

  • cleaning up, and putting me in bed.

  • I divide the day into morning, lunch, and dinner.

  • On days that I take a bath, I'll ask a helper to stay longer.

  • On weekends, I'm off work , so I like to go out.

  • I will plan my helpers' shifts 1 month in advance.

  • I am able to lead a life thanks to my helpers, though

  • there are limits on what they can do to help.

  • It's not like I can ask them to do anything I want.

  • Regarding hours of assistance,

  • we have been asking Edogawa ward office for so many years.

  • The more severe your disabilities are, the more assistance hours you need.

  • However, Edogawa ward office can't give us that many hours.

  • It's a long term problem that we have to figure out.

  • Even with severe disabilities, you can't get assistant services 24-7.

  • We'd like to have more help.

  • Going into making the documentary I didn't quite realize the amount of care needed.

  • So I asked Josh how it felt to have a helper with him for many hours of the day.

  • Having a helper helps me do a lot of things obviously.

  • But at the same time it's nice to have personal time.

  • And you know, not necessarily always having someone beside you.

  • But the problem is also because of there's a lot of personal care things I can't do on my own.

  • So I am limited by how long I can be on my own.

  • And so yeah it can be kind of a fifth wheel

  • so it can be difficult to go out with your personal friends.

  • and have another person around sometimes.

  • But at the same time, you know, if I need to use the washroom,

  • I need to have that person somewhere nearby.

  • So sometimes you get people to come with you and just wait somewhere.

  • But some companies that dispatch the helpers

  • they're worried that they might get in trouble from the city if

  • the person's not nearby to help you.

  • So they don't like you to tell them to wait somewhere completely far off.

  • So it can be a bit difficult for your personal life sometimes.

  • As Yuriko said her husband acts as her helper

  • when she wants to go out and do everyday activities like shopping.

  • She finds department stores are very wheelchair accessible.

  • This is because some of the small and older family-run stores,

  • that were built many years ago,

  • don't always have the same space to accommodate wheelchairs.

  • What should we get? Tomatoes?

  • Tomatoes and cucumbers.

  • I want more!

  • Hmm... what should we get?

  • What about the last one in this row? Tuna. The last one in the middle.

  • This is real.

  • As you can see in department stores, which often have supermarkets,

  • there's plenty of space for her wheelchair.

  • And yeah, that's the Ghostbusters theme song!

  • It's over there in the middle section.

  • What's also nice about Japanese department stores

  • is they often have a section of ready-to-go food which is found on the lower floor.

  • Can you get this, please? Yes, one please.

  • While some older style buildings simply don't have the space,

  • some do have little ramps like this which help bridge the gap.

  • It was 28 years ago when I was in the accident,

  • and back then I didn't know anything about the system at all.

  • Because I was living with parents at home and

  • living in a care home center, I didn't know about the system.

  • But since I came to Tokyo and started to live on my own

  • I stared to get interested in learning the care system.

  • If I think about it,

  • the system has been a lot changed.

  • The biggest change is that you can live on your own

  • with the home help

  • and assistant services.

  • Talking about our office's helper service,

  • ours is very different from the ones at other places.

  • We don't call it help. We call it support.

  • We respect the person who has the disability and how he/she wants to live life

  • and focus on what kind of support

  • he/she needs.

  • That is our main focus.

  • I feel that other helper service offices

  • don't really focus on what disabled people want.

  • So they help their clients with what they think they need, not what the client says they want.

  • The big difference is we understand their needs (because we're disabled too).

  • That's the biggest difference.

  • Money?

  • We provide a service, so

  • we charge our clients.

  • We're not doing this to making money though.

  • We want to support people with disabilities so that they can live on their own.

  • That is our purpose.

  • Josh lives in a home specially adapted for wheelchairs.

  • Actually, the whole apartment is designed to be barrier-free.

  • Japanese houses, but not only houses,

  • also a lot of buildings and businesses have a genkan

  • I push a button here.

  • So did you have to get that specially installed?

  • Yeah, so the city, paid for I think about ninety percent of it.

  • So in most houses in Japan, and you've probably seen them in Greg's house,

  • there's a genkan at the front which is a step that sort of separates the outside

  • from the inside of the house and what's clean what's not clean

  • so people will take off their slippers at that point.

  • But obviously it's not very accessible for people in wheelchairs.

  • So in my apartment building what they've done is made the genkan go away.

  • And so instead of having an actual genkan there's just sort of a

  • separator in the floor type so that you can say okay this is outside and this is inside.

  • So people take off their shoes there

  • so it's one of the adaptions they've made for my apartment.

  • So we've already seen the genkan and automatic door the front.

  • There's a couple other things that are sort of unique to my apartment.

  • The floor is a bit flatter than a lot of other places.

  • There used to be a door here but I had taken out.

  • It's a sliding door.

  • That's another thing as well, a lot of places in Japan they have doors that open by pulling,

  • but that's obviously difficult to do in a wheelchair.

  • So a lot of places in my apartment building , which is designed for people with disabilities,

  • have sliding doors instead.

  • Now I never ever cook, but if I ever was so inclined to,

  • Underneath the sink and the gas range they've cut everything away,

  • so I could pull in with the wheelchair, theoretically.

  • But I've, ah, I have it filled up with garbage and beer instead so...

  • And if we head over here...

  • (this) is the washroom area.

  • The bathroom is a bit bigger than normal, and also it's got the sliding doors on it.

  • Pull right up and use the toothbrush and I can get at the sink and everything .

  • And in the bathtub here, they've added these things called a sunoko.

  • Which sort of looks like a fence laid down on its side.

  • And the bathtub actually goes down about, maybe, five centimeters or so.

  • It would normally go in but they've built up these sunoko

  • so that I could drive right in with my wheelchair.

  • They've also got a number of different handles on stuff on the inside as well.

  • And then moving back here...

  • - This is Adachi-san, right? - Yeah this is my helper Adachi-san

  • And over here I've got my bed and

  • it's sort of like a hospital bed so you can lift up the feet and stuff like that .

  • So the city help pay for the cost, part of the cost of my bed.

  • On the side of the bed in that sort of tangle of cords,

  • is the interphone and normally that is sort of on the side of the wall somewhere.

  • But because if I'm in bed, I can't open the door if it's on the wall

  • and so I was able to put the interphone next to my bed so

  • whenever somebody comes in the morning to help me get out of bed then I can open the door.

  • And then once when my dad was visiting

  • he went to the local hardware store

  • and he bought some wood and he made a fence for me, ah sorry,

  • the ramp to go outside.

  • This is my pet rabbit. Usha, you're famous!

  • I never particularly was like, oh, I really want to rabbit

  • It was more that I didn't want

  • a dog because I wouldn't be able to take care of him well enough I didn't think.

  • And also a cat I was afraid that if he ran away I wouldn't be able to chase after him.

  • And so this is sort of the easiest thing to take care of that has a personality.

  • And so this is where I spend too much time probably, in front of my TV.

  • Which also has the computer there so I

  • do a lot of my work there as well as just relaxing.

  • And I have this table that is adjustable and also movable and that you know

  • I can use for dinner or for putting the keyboard and stuff like that so...

  • It's all about adaptations.

  • So there are group homes in japan so people with disabilities will maybe

  • live in the same house and there would be staff that could take care of their needs

  • And these will be subsidized by the government in some way.

  • And unfortunately that's probably, they used to the norm,

  • but a lot of people moving to independent living in the big cities

  • So where they will have helpers come for a certain number of hours a day

  • and they can do things more freely but

  • that's obviously depending on staff and as you move out into the country

  • then there are fewer for people who can help.

  • So it's just not feasible to run some sort of independent living helping program.

  • So people either move in to the cities

  • or they live in a local group home or something like that.

  • And group homes do exist inside the city as well.

  • And so it probably, depending on the needs of the person with disability

  • If they have developmental challenges or something like that or need

  • some more intensive assistance then that would probably be where they go but

  • otherwise people would maybe live on their kind of thing, so...

  • Something I was quite curious about

  • was how the general public treated disabled people.

  • One of the reasons is that I used to read about Japan's disabled being hidden away

  • And when I started living in Japan,

  • I'd have to say that I didn't seem to see as many disabled people out and about

  • as I would in Canada.

  • What I found out, is a lot has changed in Japan over the past couple decades.

  • I think in Canada people with disabilities were much more active in society for a longer time.

  • So people are maybe more used to seeing people in wheelchairs.

  • When I first came to visit Japan about 12 years ago,

  • at that time there really weren't as many people out in wheelchairs at the time.

  • So I got, on top of being a foreigner of course,

  • I got the extra, you know, looks of being somebody in a wheelchair.

  • And, your know, I think people were not necessarily...

  • I think it's very intriguing and maybe encourage people I think.

  • So at that time as I got a lot of looks and the sort of special treatment is kind of odd.

  • But even in the past couple years, I've sort of, in a good way,

  • sort of blended in with everybody else and you know it's...

  • people are more used to seeing people with disabilities out in the streets and in society.

  • And so I think everybody sort of gotten used to which is a great thing I think, so...

  • In US they know about ladies first.

  • And they take care of child or lady.

  • But in Japan they are samurai, samurai culture,

  • so they don't know how to treat (a) weak person.

  • So I think Japanese people

  • should know how to support more weaker person.

  • So I think in Canada, probably, people are a bit more upfront

  • and they'll come up to you ask if you need help and stuff like that.

  • Whereas in Japan people can often be quite like shy.

  • And, you know it depends on the situation, but maybe somebody might find that

  • the people don't care or something like that but I don't think that's the case I think

  • the other person is very aware

  • of something but they don't, they're worried they might offend you or

  • or they're quite shy because you know if you don't

  • they don't know how to react maybe

  • like if you need help or if you don't help so,

  • I think maybe you might find

  • less help in Japan, but at the same if you're a foreigner,

  • Then you also might find more help.

  • So it really depends on a lot of case by case I think.

  • But for the most part I think people are

  • very eager to help but just not sure exactly what's best so

  • Maybe they are just confused

  • And so they are honest, Japanese people are honest.

  • But they don't know, just don't know how to treat or how to support disabled people.

  • There are special school for disabled people.

  • So they cannot go (to a) regular school.

  • So they're separated between normal kids and disabled kids.

  • So kids don't know how to support disabled kids

  • And become adult. It's very program, sorry problem.

  • Yeah so that's a

  • an area where I think probably Japan needs to work a little bit more on.

  • There are a lot more separate schools for people with disabilities.

  • In Canada when I was growing up there had been separate schools,

  • but my mom worked really hard to make sure that I was always included with everything.

  • And so when I went to kindergarten,

  • I went to a normal school and I

  • grew up with the same kids up until elementary and then high school.

  • And so I attended a normal school and there were maybe,

  • in our area, there's a class that was specially dedicated for people with disabilities

  • that maybe couldn't go in with the regular stream

  • but they were still included in the same school building.

  • Whereas a lot of times in Japan, up until recently,

  • a lot of people have been, you know, they go to separate school.

  • And sometimes unfortunately,

  • it would be just because of physical disability not necessarily

  • to do with an ability to learn.

  • And so somebody with (a) normal ability to learn,

  • would be going to that school and would have to

  • wouldn't be getting the same education as at a regular school.

  • Now things are changing, there are obviously exception to those things, but um...

  • I think a lot of times a lot of the kids are more in the sheltered kind of

  • life here than they are maybe in Japan, or sorry than in Canada.

  • Recently on the news actually, for children with disabilities that are

  • maybe five or six years old

  • but they have trouble walking and they're not quite big enough for a wheelchair.

  • So they'll use some sort of special adapted stroller.

  • But because it's not really something that was really recognized in Japan

  • they wouldn't get the same help as somebody in a wheelchair even though it was necessary

  • So if they go to a station,

  • the station attendant wouldn't help them with the slope or something like that.

  • And they'd get a lot of looks because why is this big kid in a stroller?

  • So there's been a campaign to make these little stickers to put on the stroller wheelchair.

  • To raise awareness so...

  • People are getting out and more involved now but

  • there are some ways I think it's not as advanced or progressive as Canada is.

  • In comparison to other societies, Japanese like to follow rules

  • This means a well organized society

  • but at the same time it can mean it's difficult for people to bend the rules for special cases.

  • And I've come across a couple times where

  • it's maybe not necessarily following the rules but

  • if they let me do this them I can enjoy

  • whatever it is I'm trying to enjoy in the same manner as everybody else.

  • but it's just a little bit different, but,

  • ah, you know, because the staff

  • know the rules and they're maybe not

  • in a position to make the decision on their own

  • they'll just be hesitant to try and they'll just say no instead.

  • For example I went to a train museum

  • and I wanted to look at this one display

  • where they're having a show for these mini trains or something and

  • I wanted to just go up to the display and look at it

  • but i was told by the staff, no, no, people in wheelchairs watch from here.

  • And I say, but the show hasn't started yet.

  • And so I just want to go look, I'll come back, don't worry.

  • And, yep, yep, nope, but you know if there's a fire...

  • or something happens then you'll get in the way of other people.

  • And even if there's the plenty of room and there's barely anybody there

  • and it's just those the rules and that person didn't

  • feel they had the authorities to say, ah, it's ok, you can go.

  • You know where as, maybe

  • in places like where more individuality and

  • taking a lot more personal responsibility they'd be like, ah, it's ok, you can go for it, I understand.

  • In Japan sometimes you come across like...

  • I don't think we can do that because we've never done that before and so we don't want to try.

  • Which can be a bit difficult for people with disabilities, with different disabilities particularly.

  • In Japan, just because of the living conditions of, you know, everybody,

  • There's not a lot of space, especially in Tokyo.

  • So maybe people who are used to North American sized buildings

  • might be surprised by the the compactness of stores here

  • and that can cause a bit of a problem sometimes if you're in a wheelchair

  • because you just can't get through.

  • If you go to a Japanese style restaurant in a brand new

  • office building or something like that

  • they'll often have a step that they've artificially built there because it feels traditional.

  • It can be a bit sad sometimes when you want to go out somewhere and

  • you can't get in even though it's a new building and you should be able to get in

  • When I was diagnosed with my disease

  • there were no elevators at my station.

  • So, but, (when) I began to use (a) wheelchair

  • when I was 26 years old, in 2006,

  • they installed an elevator.

  • So it's very good for me to go outside using public transportation.

  • So it became easier to go outside for wheelchair users. It became accessible.

  • And 2020 there will be held Olympics and Paralympics,

  • so Japan will be more accessible.

  • Yeah I think that Canada definitely has an

  • image as being a very progressive country and I think it is for sure.

  • But Japan, while it was playing a bit of catch-up,

  • I think it's even surpassed Canada now, in many ways.

  • For example, I can use a lot of the Japanese services for

  • having personal care attendants come.

  • And I get actually more time than I was getting in Canada.

  • In addition to that I think the biggest thing, for me anyways,

  • is I was living in the country in Canada out in the middle of nowhere

  • and if you don't have a car then you can't go anywhere.

  • And everything depends on asking people for rides and

  • on top of that if you use a wheelchair then you have to have an adapted vehicle which can cost

  • maybe $80,000 or a hundred thousand dollars.

  • And sometimes you get money from the government but it's only

  • maybe $20,000 or something like so you have to pay the rest yourself.

  • So you're really limited in where you can go and everything.

  • Where as when I came to Japan, living in a big city,

  • with an incredible infrastructure for getting around in trains and such,

  • it's really opened up a lot of

  • my world here and so I can go to so many different places by myself.

  • And live a very full life here.

  • As much as there are great facilities in Japan,

  • knowing how to best access them can be a challenge

  • Yuriko recognized this and entered a Google Impact Challenge contest

  • I got grand prize from Google Impact Challenge,

  • so that is financial support.

  • I want to build new application, app, for wheelchair users.

  • The idea is a barrier free and accessible map

  • which will be created by collecting user submitted data on barrier-free routes and facilities.

  • In this project I learned a lot about what it's like to live with a disability in Japan

  • and the government supports in place.

  • Much has changed in the past 20 years,

  • and in fact, just in 2016, a new law to eliminate discrimination

  • against people with disabilities has been enacted.

  • Some have felt that the new law doesn't go far enough.

  • But I do think it's a sign that changes are going in a positive direction.

  • Living in Japan with a disability is by no means perfect,

  • but it's good to see that the advocacy work of people like Josh,

  • Yuriko, and Tsuchiya-san are improving things.

  • When you've never tried something before, you don't think you can do it. We want you to challenge yourself and try things you can't do.

  • You'll then realize it's not that hard to do,

  • and there was no reason to have not tried before.

  • We want them to realize that making a small step is really important.

  • That's what I think.

  • If you just don't try taking a small step forward,

  • you'll just give up on one thing after another.

  • I want to share our experiences with them

  • and continue to improve our services.

  • I'd like to give special thanks to Yuriko, Josh, Tsuchiya-san, and Adachi-san

  • for letting me interview them.

  • Also thanks to Agatha for assisting me.

  • Yuriko has a great series on YouTube

  • about traveling around japan and the world in a wheelchair,

  • so make sure to check it out!

  • Josh is the guy behind Accessible Japan,

  • which is an English site that helps people with disabilities navigate Japan.

  • So make sure to check that out too!

  • And thanks to all those who have supported these documentaries on Patreon.

  • As always, thanks for watching, and I'll catch you on the flip side!

I'm Yuriko Oda and my disease is distal myopathy

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