Access Denied Diaries

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#AccessDeniedDiaries by Susan preview image

#AccessDeniedDiaries by Susan

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I encounter access barriers whenever I am out and about with my white cane, especially when I am alone. I am grabbed, pulled, shouted at, patted, questioned, 'helped' without asking, and harassed by the public. Every time the environment I'm in makes me visibly struggle - in the eyes of others - it reinforces the idea that disabled people always require help and 'saving'. Every time a disabled person encounters a barrier that causes them to stay at home, it makes seeing people with disabilities - going about their daily lives - an even rarer sight. Access barriers - combined with a lack of education and public information - make those disabled people who are getting on with their lives, out and about in public, to be viewed as somehow extraordinary, or heroic, or even a cause for panic! This is a social media post I wrote two years ago. It is as true now as it was then: Social Distancing: The Perfect Time to Stop Grabbing Disabled People. “Surely people have stopped touching you now?” I wish. Let me share the story of my day, 19th March 2020. I am functionally blind. I walk competently with my white cane, and I am always grabbed by strangers without consent. Today I counted. I caught and changed buses, walked to the doctor’s, the fruit and veg shop, and the supermarket. Total walking, about five blocks. In that short time I was pushed, pulled or patted by five different strangers, all on my shoulders. Usually it was the first I even knew they were there. Two people also snapped at me. The first snapper didn’t actually touch me. This person asked four times if I needed help off the bus, despite my firm “No thanks” reply each time. They then shrieked at me when I felt for the ground with my foot. I said I didn’t need help simply getting off a bus. They muttered behind my back, presumably about how rude I was. The second snapper was a man who patted me on the arm at a pedestrian crossing. I moved away, but when I was crossing went he put a hand on my shoulder and pulled, saying, “Here I’ll help you." I said, “Please don’t touch me without asking.” He snapped, “Be like that,” and stormed off. I am not sharing this because my story is unusual. It wasn’t even a bad day. This treatment is my normal. In the past I have been gripped and pulled by my wrist, grabbed, pushed and pulled by my shoulders, around my waist, my hands, and even my backpack. My white cane is also often grabbed, this leaves me vulnerable and unable to sense my surroundings. I’ve been screamed at, sworn at, snapped at, ignored, disbelieved and told I should be grateful. I know that people often ‘mean well’, but at the end of the day, actions speak louder than intentions. Barring some life or death scenario, it is never acceptable to touch someone without consent. To clarify, being a disabled person in public is not life or death. Pulling me towards a drop could be. But it happens. It happens to all my disabled friends too, whether they are blind, or are wheelchair users, use other mobility aids, etc. It happens to disabled people all over the world. Here’s what we need from you. Never ever touch a disabled person, or our mobility aids, without consent. Stand beside us, support us, as we stand up to those who do try to non-consensually touch us. Educate your friends. Call out those who won’t stop. Never ever defend it by saying, “They’re just trying to help”. Please share. I have made this post public so that you can. Many people don’t even know this is a problem disabled people face. COVID-19 social distancing highlighted another layer of danger. I am asthmatic. Most of the people I know are vulnerable. But I cannot keep myself or those around me safe because personal space is not a right disabled people get. I want the Government's new access law to remove the barriers - physical, financial and social - to disabled people's access to public spaces, activities and general life. Accessibility legislation should increase education and public awareness. And the Government should lead by example in treating disabled people as valuable and respected members of society.
#AccessDeniedDiaries by SW preview image

#AccessDeniedDiaries by SW

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I encounter an access barrier every time I try to go to the movies. Not a single cinema, that I know of in Aotearoa New Zealand, routinely provides audio descriptions for its films. Overseas cinemas have headsets to listen to the audio description track, so blind and low vision patrons like me can follow the film. The audio description tracks already exist. They are made by the movie producers and released with the film. The cinemas don't have to create anything! They just have to provide a few headsets, sync the track up, and play it. It's as simple as broadcasting subtitles, or the soundtrack at a higher volume - which are not perfect solutions from what I have heard from d/Deaf folks, but at least d/Deaf people get something to make movies accessible. I have to pick the films I see based on whether or not I think I have any chance of following them. I often have to go home and Google the movie to find out what happened at the end! If I am with a friend, they will whisper descriptions in my ear the whole way through the movie. This is so lovely of them, but it is extra work, and it's socially awkward for both of us. Audio description headsets - and the cinema's willingness make the audio description track available - would let me access movies equally with others when out watching films. The new access laws should make businesses meet reasonable standards of accessibility, including providing access for blind and low vision patrons. New Zealand businesses should provide an equal level of access for all their customers, as is required of businesses in countries overseas that have good accessibility legislation.
#AccessDeniedDiaries by Gerard preview image

#AccessDeniedDiaries by Gerard

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I have been denied access to an appropriate benefit from the Ministry of Social Development (MSD) because of my disabilities. MSD treats people with disabilities the same way they treat abled people. That is, MSD will provide as little financial assistance as they can get away with. The underlying rationale being, if beneficiaries are denied a livable benefit, then they will have to accept any form of employment in order to make ends meet. There are many beneficiaries with disabilities who aren't able to work, including myself.  This fact doesn't enter into MSD thinking. And no matter how much hardship MSD places us in, we still aren't able to work. MSD refuses to acknowledge that there are people needing financial assistance who would love to work but aren't able to. By denying people with disabilities a reasonable benefit, MSD is not only breaking their own obligations under the Social Security Act 2018, but they are also flagrantly denying their obligations under the United Nations Convention on the Rights of Persons with Disabilities (UNCRPD). MSD can do this because there is no independent body with the appropriate authority to hold them to account. My disabilities, amongst other issues, include Traumatic Brain Injury (TBI) and brain damage in general. My ability to comprehend information is severely compromised and massively exacerbated by stress, as well as other negative stimuli, such as noise and other distractions. These conditions all exist at MSD offices due to their preferred choice of design - open plan office layouts. In addition, the use of commercial lighting brings on migraines and my inability to tolerate any Volatile Organic Compounds (VOC) - such as perfumes, fragrances, cleaning chemicals, etc, all of which are continually recirculated through the 'air-conditioning' system - make any visit to an MSD office absolutely brutal! Add up all the above mentioned stress into the mix - with staff who don't want to hear you, and don't want to assist you, and try to as unhelpful as possible - then it's no big surprise that I end up in tears again and again after each appointment. It is no understatement to say that I now also suffer from Post Traumatic Stress Disorder (PTSD) because of the continual abuse I have had to endure from MSD. It will probably come as no surprise that I prefer to live in a vehicle rather than deal with the chronic abuse and stress I have had to endure from MSD. The fact that I have been living in a vehicle, for 20 years, reflects poorly on a system that just doesn't care. The new accessibility act needs to look beyond the narrow scope of physical and/or sensory disabilities - such as having low vision or being hearing impaired - and consider the broader definition of disability as outlined in the UNCRPD.
#AccessDeniedDiaries by Anamaria preview image

#AccessDeniedDiaries by Anamaria

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We are trying to get some support for my teenage Moko who has a brain injury after being reversed over by a vehicle, aged 18 months, never to be the same again. Four years after his accident, an MRI suggested he has pachygyria, which causes Fetal Alcohol Spectrum Disorder (FASD). The Accident Compensation Corporation (ACC) denied his injury claim on the basis that he has FASD, which ACC says overrides the accident. However an official FASD assessment has never been completed. We need the official FASD assessment to be able to move forward but the cost is huge, at over $6500! We have been denied the accident claim after 16 years of battling ACC, and every other government agency. In addition, Whanganui Hospital did not correctly record the original accident, and have refused to amend it. This has also stopped us being able to access support. We get shoved off every time. How is this young man supposed to manage in the community? He has hardly attended school due to no school being able to cope with his behaviours, no matter how many strategies the specialists provide for the principals and teachers. Who decides who gets help and who does not? What qualifications do the people in the agencies actually have? Are they even qualified enough to be running these agencies?! Why do you have to continue to prove that your child has a disability, when it's been repeatedly confirmed by top specialists? How can an agency demand yet another assessment, by people less qualified, to override a specialist opinion, so that my child will not qualify for help? Why is the Needs Assessment and Service Coordination service (NASC) stopping families in Whanganui from getting the necessary help they need for their children with disabilities? These access barriers have stopped my Moko making progress. This is a burden we bear every day. It takes up so much time, and constant changes in medical staff make it even more complex. We are often told that there are other people who are way worse off than my Moko. Cold comfort. We continue to get brushed off due to incorrect information on my Moko's medical file. I am told it cannot be removed or amended, after trying many times. I have been in touch with the top pachygyria specialist in the world who has confirmed my child does NOT have pachygyria. They have asked for another MRI to be completed, but we are constantly refused this service, and this concerns me. Each specialist we visit has a new spiel on my Moko's medical condition; taking it out of context and removing it as far away as possible from the original accident. The ACC medical team are the worst at making my Moko's medical history complex. They overrode our specialist, who was our main provider. This all makes me feel undervalued as a caregiver/parent, and this has been am extra barrier to being able to source the correct support. I should not have to battle at every corner. I am asked to jump through all these hoops only to be told we do not meet the criteria, and that it is an ACC issue. I have fought ACC for 16 years, with the last five years in court, only for them to close the door on us. ACC insists my Moko's condition is FASD, when there is has been no official FASD assessment. It is exhausting and dehumanizing. I have been made to feel worthless and unvalued. I have been bullied by many agencies, medical professionals, ACC, lawyers, teachers, WINZ, ACC specialists and sporting coaches. I have exhausted all avenues, including writing to Members of Parliament, the Human Rights Commission, the Children's Commissioner's office, the Race Relations officer, the Minister of Education, the Minister of Health and Disabilities, you name it. They simply dismiss me by referring me to the Advocate of Ministry of Health and Disabilities. It's endless. :( What processes can be put in place to remove incorrect medical information from someone's medical file, especially when it hinders the person? Where can we source funding to pay for additional assessments like FASD? I would like to see a Special Needs Teacher Training School set up. We had a teacher from England come into my home to teach my Moko.  She had special needs teacher-training and her skills were precious. However it was only for a short time as she took up a teacher's position in a school. Her time with my Moko showed he can improve in his school work. I want the law changed! I want all people, with any type of disability, to have easy access to an effective advocate. So that parents can get on with caring, and be able to get the necessary support much more easily. Accessibility legislation should allow all children to attend school, with funding for extra specialist teachers whenever necessary.
#AccessDeniedDiaries by Michael preview image

#AccessDeniedDiaries by Michael

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Welly Wellington ... capital of New Zealand, but not for the disabled! I recently visited Wellington, from the South Island, for a two-night stay.  I attended a one-day workshop about volunteering and Not For Profit governance. I was appalled, to say the least, at the lack of disability services available. Namely Powerchair transport. Having gained great confidence using my one-year-old Powerchair, which has allowed me to become very independent, I was dismayed when I began to research my transport options in Wellington. A bus service that was on hold until 1 July (just some airport bus I believe). And not much information about other buses, for example how far from the airport the nearest stop is to get into the CBD. Or if I could get there without getting wet should it be raining. I was disappointed to read there are very few options for mobility taxis that accommodate wheelchairs and Powerchairs, especially after 7pm. What’s with that? Other taxis run 24/7 and so do Ubers. Are the regulators at fault making it too difficult to provide such a service? At least 48hrs notice for a booking, they say, and even then it not 100% reliable. You could easily get hung out to dry (if it’s not raining!). The mobility taxi reviews scared me, quite frankly. I reneged and swapped my Powerchair for my smaller, foldable electric chair - which has no where near the functionality of my life-changing Powerchair. This is compared to Christchurch which has a smaller population base and yet offers a number of mobility taxi options all day and most of the night. (Maybe I just have good contacts in Christchurch?) To my mind it's quite unfair that, as a disabled person, I am so restricted. Manaakitanga indeed! This just seems to be the latest “in word” for government and local agencies. We need more than lip-service and platitudes. We need comprehensive accessibility legislation, that allows everyone - no matter the city or town, no matter the time of day or night - equitable access to services including transport. Perhaps I was not reading the right information about Wellington's disability transport services. I would be pleased if someone told me I was wrong. It might convince me to visit again.
#AccessDeniedDiaries by Sue preview image

#AccessDeniedDiaries by Sue

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Grocery shopping since COVID-19 lockdowns, isolation and social distancing, has become quite traumatic for me, both online and in person at the supermarket. It is a necessity that I now dread doing each week. So much so that anxiety creeps in whenever it's grocery shopping time. Of course, like many households, it is much easier to get the groceries delivered via online shopping, so I do my main shop online each week. But also, like many people who find themselves the main shopper, there are those times when you only need that one item you forgot to order (or wasn't supplied!) or those couple of perishable items (milk, bread, fruit 'n' veggies) that I find myself needing to go through the drama of doing a small shop at the supermarket. Firstly, online home delivered shopping The online buying part is reasonably smooth. Yes, I allow substitutions, as I need all the items on the list! Some of the personal shoppers need more education on what a suitable substitute is, but that would be another whole story. So, I'm told my order will arrive between this time and that, IF they don't go and change the delivery time! Then in rolls the delivery truck. The groceries are placed completely blocking my entrance door, even though I'm signalling to them - from inside, behind a huge ranch slider window - to place the groceries to one side. So yes, the driver can clearly see I'm in a wheelchair and that I'm waving my hands, and yelling to them to please move the groceries and place them on the table and bench I have set up on the deck specifically for deliveries. The driver leaves and I am stuck having to lift the groceries off the ground, one bag at a time, and bring them inside. This is a massive feat for me with my weakness and balance issues.  I don't understand why the driver hasn't followed the Delivery Instructions that I’ve painstakingly written for them! I also don't understand why - especially at this current alert/traffic-light/lockdown level, when everyone else is allowed into my home - the supermarket delivery drivers are still not allowed to place the shopping bags in my kitchen for me. Oh, I remember pre-COVID-19, when that little act of kindness was done, and it was greatly appreciated! However, if I need anything else, I'm stuck having to go in person to the supermarket (unless I want to spend another $80, even though I have bought the delivery package!) Secondly, in-person supermarket shopping. So, off I go with my one reusable shopping bag. I only want to buy a couple of things, and if I restrict myself to one bag then I know I can manage carrying that amount.  I'm then told, on arrival, I'm not allowed my bag in the shop because of "contamination issues". But my clothes are OK? Are you sure you don't want me to strip before entering? So the reusable bag goes back to my car. I come back, grab a basket, and head into the shop. Social distancing is in place. Two metres away from people. I will obey! Hmmmm. So why do other people reach over me, breathing potential COVID onto me from above? It's like, because I'm in a wheelchair, I am not human? So the 2-metre rule doesn't apply?!!! So rude and unbelievable, but it happens all the time. (I try to run over their toes but usually miss as they are scuttling around so fast!) Bread, milk, and the forgotten or omitted item in hand, I head to the checkout. It's my turn. "Morning," says the checkout person, and I reply a cheerful, "Morning! How's your day going?" No reply. Hmmm. OK. I notice the checkout person doesn't look at me, but is instead glancing at the lady behind me. I roll up to the EFTPOS machine and wait patiently. The checkout person picks up the milk and notices it's leaking, "I will get a replacement for you." "Thanks!" I respond, as she gives me a sideways scowl. OK that's weird. I sit and wait. I place my scanned items back in the basket. The milk arrives. It's scanned and into the basket it goes. "Will that be all?" she asks, looking at the next customer. "Yes," I reply. "Excuse me, will that be all?" she asks the next customer. Louder, I say, "Yes thanks!" The checkout person again scowls at me then asks, "Do you need something?" "No," I say, not so pleased now, "YES! I'd like to pay for my items please." Her rather rude response was, "Well I'm just finishing this order!" My rather abrupt response was, "This is my order, not that person's!" Next she really annoyed me with a condescending, "Well, where is your helper sweetie?" "I DONT HAVE A CAREGIVER. I'M CAPABLE OF DOING MY OWN SHOPPING AND I'D LIKE TO PAY FOR IT AND LEAVE!" Well, she took my money and finished the transaction without another word. "Thanks so much," I say as I turn to roll away, only to find a supervisor and a security guard has appeared! I wheel around them and head towards the exit. The guard then stops me, "You can't take the basket outside." I explained and pointed to my car, saying, "You didn't allow me to bring in my bag, so surely I can take the basket the 20 metres to my car, empty it, then return it?" The answer? "NO!" "OK can I leave the basket here and go grab my bag from the car?" I ask. Another "NO!" from the security guard. So I empty the basket and try to balance the groceries on my lap. It doesn't work. I ask to buy a 20c bag but they won't do an EFTPOS transaction for that amount. I place the basket at the guard's feet, grab one item, and say, "I'll be back for the rest, and if anything goes missing you will be in trouble!" He suggests I leave the shop. "I'm trying to, but you're making it very difficult!" I reply. I return three times to get all the groceries. When I grab the last item I turn to the guard and say (possibly sarcastically - but hey I was fuming), "Thanks so much for all your assistance. I'll be sure to submit some feedback to the store!" Shaking by now, I return to my car and get in - all the while being watched by several sets of eyes - and leave. Never to return to THAT supermarket ever again! Time for change The attitudes of workers at our big supermarket chains need a lot of education. Let me facilitate a workshop on how to serve disabled customers: How to treat us like any other customer That a person in a wheelchair may still talk, think and shop for themselves That small accommodations - like allowing a basket to go to a vehicle, that you can see from inside the shop - can make all the difference! We need companies to stand up and educate their staff to be considerate, inclusive and accepting of all humans! We need government legislation that provides access for all, and a positive change of attitude from everyone.
#AccessDeniedDiaries by Susan preview image

#AccessDeniedDiaries by Susan

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I experienced an access barrier when I tried to cross the road in Central Wellington. I couldn't cross the road safely without getting my feet soaked. There is an awful crossing near the New World supermarket, with no tactile markers, and the signal pole is miles from the curb cut. So, as a blind person, I have to feel for the tactile signal, jump, and line myself up as best I can with only the signal box to give me an idea of the best angle to safely cross the road. If I get it right, there is a massive puddle that involves climbing over the edge of a garden to avoid. If I get it wrong, I have a choice between standing in fast traffic or navigating a short ledge into a muddy garden bed. Crossing the road in Welly is a 'fun' little game of Russian roulette. Will there be tactile markers on the footpath or will it be a curving corner that directs me into the path of traffic? Will I cross this five lane road, or end up balancing on a silly little road triangle? Will the footpath be completely impassable with roadworks? Who knows? Let's 'play'! EVERY street should be accessible. We don't put up signs saying, "No Disabled People Allowed In This Part Of The City!" So stop putting up infrastructure that says exactly the same thing. Needless to say, walking anywhere in Welly is stressful as heck. And on this particular day, my shoes did end up getting very wet. But at least I survived to tell the tale. We need accessibility legislation in Aotearoa New Zealand that requires accessible public infrastructure ... yes, even in our capital city of Wellington! This must include tactile markers at ALL pedestrian crossings, traffic light crossings and corner curb cuts. The law must require councils to actually check infrastructure for accessibility. Why should I have to report hundreds of individual lapses in access through the Council app, one by one? (Especially when I then receive a phone call at some ungodly hour of the morning regarding every single incident.) I don't mind reporting the odd fault. But if you want a full accessibility audit of the city, then hire me properly, guarantee to fix the access barrier issues, and pay me for my mahi.
#AccessDeniedDiaries by Barry preview image

#AccessDeniedDiaries by Barry

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I encountered a barrier to access when I was trying to find the correct bus to get me to my destination. I was at the central bus interchange in Dunedin and couldn't confirm the correct bus due to being Deaf and unable to quickly communicate with the bus driver. Another person was about to hop on the bus and he seemed to point elsewhere. I guessed that this was the wrong bus because it seemed the driver was trying to indicate his bus route was going uphill, whereas I wanted to go to the flat land of St Clair Beach. I hopped off the bus and walked to a different part of the interchange to try to find the correct bus - which I eventually did - but it should not be guesswork! The bus drivers, and bus IT and communication systems, need to be clear, instant and correct. Numerous, similar incidents have occurred to me before, usually when I was unable to quickly communicate with a bus driver. I have had bus transport barrier incidents happen in other cities that were more embarrassing than this one in Dunedin. For example, one evening two buses went in completely unexpected directions. I think the hearing passengers knew why, but I didn't until a transport station official finally informed me. Other passengers were looking at me as though I was an idiot or imbecile, when I was just very confused and frustrated by the diversions. It turned out to be a major route closure event, but without any notification or communications that I could access. The new accessibility legislation should make it compulsory for bus IT systems to communicate correct routes, bus stops and route alterations in captions and in New Zealand Sign Language. They should set up Bluetooth technology to enable mobile apps to query bus IT systems.
#AccessDeniedDiaries by Amy preview image

#AccessDeniedDiaries by Amy

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I encounter an access barrier dressing my young child on a daily basis. I have Postural Tachycardia Syndrome (POTS), which means I can not walk or stand for any length of time. I get out of breath really easily, and mornings are the time I am most symptomatic. I am not eligible for any support to dress and get my four-year-old ready for preschool, even though, if I needed assistance dressing or feeding myself, I would be eligible for it under personal care. The care I do for my child does not count. Like most four-year-olds, my child is not independent. When getting ready in the morning, I give her significant assistance by preparing breakfast, feeding her breakfast, dressing her and giving her medication. Also, like most four-year-olds, she is uncooperative and high energy! I am physically unable to perform all these tasks, which leaves me having to ask her ECE teachers for support. I don’t understand how I am eligible for support for my own personal care, but not for the care of my child, which is my responsibility as a parent. This morning I wasn’t able to give my child her medication. My POTS and essential tremor makes it very difficult to pour out medication doses.  Also, I am unable to physically restrain my small child to give her the medication. I was not physically able to brush her teeth well this morning either. These sort of incidents occur on a daily basis. I send my child to preschool without her basic cares completed, and have to ask the teachers there to assist me. This makes me feel inadequate as a parent, as I am unable to physically care for my child. I am, however, very grateful for the support I receive from her child care centre. I want legislation that ensures supports are provided according to need - not just my own needs but also those for whom I have responsibilities.
#AccessDeniedDiaries by Teena preview image

#AccessDeniedDiaries by Teena

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I raised my three children on my own, while living with very low vision and no family or community help. We were housebound because I had no transportation due to my sight problem. My children have suffered because I could not take them anywhere on my own. This resulted in my children not learning to swim, or playing in sport teams, or even going to friends' houses. I am also housebound because I have no family or anyone to help. My benefit is not enough to use taxis and the bus services in Bell Block, New Plymouth, are terrible. Thank goodness for the internet, at least I can get groceries on line. I would like to see accessibility laws that allow access, for those with disabilities, to the everyday activities and services that most people take for granted. Things like a more subsidised transport system, which might include perhaps three free taxi trips per month. Or maybe a payed helper for parents with disabilities, so they can take their children out. Small things that would make a big difference. My life has been extremely unfulfilling because we live in a society that just doesn't care about people who have no one to support them. I have struggled with access barriers and discrimination my whole life, partly because I was born into a family that wanted nothing to do with a disabled kid. Hopefully legal changes will also cause a positive shift in people's attitudes towards those of us with access needs.
#AccessDeniedDiaries by Vivian preview image

#AccessDeniedDiaries by Vivian

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In my experience working in the building industry, I have noticed an access barrier in the attitude of a developer who builds multi-story buildings and locates all the building’s accessible toilets in the one place – the ground floor. Although NZS 4121 advices that accessible toilets should be included where general toilets are located, this developer argues that he is providing more accessible toilets than are required by the Building Code and has persuaded Council that this is a desirable outcome. Clearly this is not to the advantage of people who need to use accessible toilets, for a range of reasons: Anyone can find themselves needing to go to the toilet urgently – what an additional stress to get the lift to the ground floor People with stomas of different kinds need a toilet and basin located together, they cannot deal with such equipment at the generic hand washing basins If there is a power failure and the lifts stop working, how do you reach an accessible toilet? Extra time is needed while waiting for the lift to and from the ground floor toilet, which is also detrimental in additional costs to the employer. There is no dignity in not being treated the same as everyone else. From a commercial perspective, the non-provision of accessible facilities on upper floors requires tenant businesses to install their own accessible toilets alongside the suite of toilets provided in the base build. It angers me that this additional expense falls on the tenant. Of course the tenant leaves that accessible toilet infrastructure in place when they terminate the lease – thereby increasing the value of the tenancy when it is leased out again - to the benefit of the building developer and owner. I am dealing with such a situation right now: one client is moving into newly renovated premises, where accessible toilets are provided on all floors, whilst another is moving into a building currently being built by the above developer. I want the new accessibility legislation to ensure the enforcement of both the spirit and the letter of access regulations and building codes. #AccessDeniedDiaries
#AccessDeniedDiaries by Shona preview image

#AccessDeniedDiaries by Shona

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I asked a life guard at my local pool about the hoist for disabled people. The life guard completely spoke over my head and ignored me. She treated me like I was stupid, even though I had asked the question. I was told no one knew how to use the hoist, but the life guard said she would love to learn how, "Oh, but the hoist is locked away. And please give us 24 hours notice when you want to come to the pool." I got angry with her. We left. I rang the council, who run the pool, but they did not instill any confidence in me with their comments either. It's not fair. This sort of access barrier is not an isolated incident. It's happened before, and not just at the pool. It's hard to get into so many shops and cafes. Plus you get stared at. I have never been back to my local pool. They scared me. They made me feel less than a person. I want accessibility legislation that will make all life guards get proper training to operate the hoists at pools. They should make the stairs more accessible for the elderly too. I also think there needs to be polices about how much stuff they can put on the floor of shop aisles as I often can't get access because of this. The same with blocked doorways. Not only that, councils need to think about how they build toilets to allow access for people with disabilities, and not put heavy doors on them. Heavy doors are really hard open for powerchair users. #AccessDeniedDiaries