The 8th Annual Toronto Disability Pride March

Save the Date: Saturday, September 22, 2018

Starting at Queens Park (111 Wellesley Street West) and marching to the School of Disability Studies at Ryerson (99 Gerrard Street East) from 1:00 PM to 4:00 PM

Why we’re Marching:

  • To bring recognition of the struggles and value of people with disabilities as we fight against ableism, sanism and other forms of oppression.
  • To be visible and show that we have a voice in our community and a right to be heard by taking to the streets.
  • To celebrate and take pride in ourselves as a community of people with disabilities.

Be Loud, Be Proud, Come March with Us!

We have a Fundraising Page and we also accept Paypal donations.

Find us on Facebook and Twitter @DisabilityPM

We need volunteers and marshals for the march! If you have experience that is great, if not we still want you! If you aren’t sure what a marshal does, here’s a brief description. Please fill out the volunteer form if you are interested.

Some  things you should know if you plan to attend.

The Toronto Disability Pride March aims to promote a cross-disability atmosphere, that also recognizes other forms of oppression such as race, class, gender, sexuality, sanism, etc.  We believe the disability movement is strongest in a harmony of voices, not one homogeneous voice. We ask all those who plan to attend the march to respect this approach and the other people within the space of the march.

Just a reminder to book your rides for the march on Saturday if needed! If you need parking, it’s a bit complicated, but not impossible. Leave us an email and we’ll message you directly if you have parking questions.

Please note: accessible washrooms are not available at Queen’s Park. Please see information on accessible washrooms on the route page.

We would also like to invite people to bring their own noisemakers to the march -maracas, tambourines, etc. 

 

Have Questions? email us at torontodisabilitypride@gmail.com .

My Letter to Mayor Tory regarding Accessibility for the TTC in the 2018 Budget

Dear Mayor Tory,

I write to you as a concerned citizen of Ward 6 Etobicoke-Lakeshore, and the City of Toronto, to request your support to continue with some accessible buses on the 501 streetcar line and other streetcar lines, and for shuttle bus service for major elevator disruptions, and that these items be reflected in the City’s budget for 2018.

Since January 2017, accessible replacement buses have been running across the 501 streetcar route during track reconstruction, this route is scheduled to return to inaccessible this month. Because the replacement buses are accessible and the streetcars are not, this construction has greatly improved my quality of life and that of many other TTC passengers.

Having accessibility on this line allows me to access my closest grocery store, rather than one much further away. It also made it possible for me to take a spontaneous trip to High Park with my young nephews. It made my trips from downtown shorter by half; a particularly safer option for a young woman such as myself when travelling at night to visit friends. I’ve also seen seniors have a much easier time getting to St. Joseph’s Hospital because of the accessibility on that line.

I’m not suggesting we stop having streetcars. Streetcars transport more people than buses, and that’s important. I also know that even if the TTC had all of the new accessible streetcars it ordered from Bombardier, we would still have old streetcars on that line, not enough streetcars were ordered to fully replace them. In short, there is no plan in place to return accessibility on the 501 route to levels experienced in 2017. If the 511 streetcar route can have buses due to a lack of accessible streetcars, the same can be done for the 501, and other routes.

Earlier this year, the elevator was down at Yonge and Bloor station, denying me and many others access to the Bloor line from that station for over a week. At Kennedy Station, that elevator has been down since October and is not scheduled to come back in service until January. The next closest accessible station is Victoria Park. There’s no shuttle service set up between stations either. It’s understandable that sometimes elevators break down, but passengers who use the elevators deserve shuttle buses just as they would have during any other service disruption.

In a world class city like Toronto, we know that people with disabilities deserve equitable service, on the TTC, and that starts with giving passengers with disabilities equitable dignity, respect, and consideration.  The budget for the TTC should reflect that as well.

“We Need Not Remake the Past” – The Future of the Disability Movement

Presentation at the Canadian Disability Studies Association Conference 2017

Thank you to my fellow organizers and panelists. Before I get started, I’d like to identify myself within this conversation, as a white, employed person with a physical disability that is easily identified with, and the privilege that comes with those things. I also identify as a radical disability activist, knowing that I’m someone who has the privilege to be able to identify myself in that way without much repercussion. The presentation I’m giving today and the research behind it are given in recognition of that privilege, and knowing that the knowledge I share has built on the knowledge of others who may not have these privileges.

I’m also the founder and co-organizer of an annual event called the Toronto Disability Pride March, now in its 7th year. For those of you who may not be familiar with the march, it is a grassroots event lead by a small team of dedicated organizers. We highlight issues facing the disability and mad communities, and by prioritizing the voices of those of us who are the most marginalized. We recognize that the mad and disability communities are as diverse as the communities we come from, while turning privilege on its head. This is reflected in the speakers we call upon each year, but also in our organizing team. Our social media discusses subjects ranging from accessibility standards to Black Lives Matter and Idle No More to labor struggles, the lack of housing in Toronto, and the struggles faced by the many people living in poverty. It’s an amazing bubble of disability justice organizing that we’ve been fortunate to steep ourselves in for the last eight years without any government funded restrictions on the activism we do.

Like many such social justice bubbles, it becomes seductively simple to forget or overlook the reality that most disabled and mad people in Canada do not have these spaces. If these spaces do exist are often much less diverse and harder to plug into, they may seem detached or elite, or simply don’t connect with the day-to-day realities of people’s lives. Many disabled and mad people are connected in small local networks, but a great many others are on their own and left to tackle issues of oppression and discrimination in an individual way.

I’m going to be exploring two main groups of disability organizations today what I refer to as grassroots disability organizations and legacy disability organizations. Grassroots disability organizations are smaller, local organizations with minimal funding or structure, with a focus on a particular disability issue or event. The organizations have a short history, and they often make use of intersectional discussions and social media to increase public awareness to build political pressure in creating change. Legacy organizations tend to focus more on policy and programs, they have a long history usually spanning over decades, and have built strong relationships with governments, and potential funding organizations.

While grassroots disability groups have difficulty connecting with older legacy organizations, the reverse is also true. Legacy organizations seem to do their work outside of what’s happening on the grassroots level. It is the segregation between these two groups that brought about the research I present here. Some time ago I was asked to participate in a research project by legacy organization, asking why younger disabled people weren’t participating in activism. I don’t have my response, but it started with something like “perhaps we should re-examine this question”, and so I am.

To illustrate the bias in the research question of why younger disabled people aren’t participating in activism, allow me to use the example of a poverty group that I worked with back in the early 2000s. The group had a board structure, and was comprised of 50% community members who were people living on ODSP, and 50% service providers such as legal clinic workers and social workers. I sat in both categories as a social work student living on ODSP, and within a few years I was asked to Chair the group. By taking on that role I came to realize why the group had such difficulty communicating. While both sides of the table shared the goal of eliminating poverty, the two sides were not equal. There was a clear power imbalance between the two sides that the structure of the committee could not address. Different priorities in both the structure and goals of the committee were very clear, and both sides looked to me, as the Chair, to prioritize the needs of their group.

The bias is that legacy organizations have failed to acknowledge that a conflict between grassroots and legacy disability organizations exists, or that they may have some role in the conflict. While each group is passionate about disability rights, they end up competing for talking points within larger institutions, rather than working in tandem with each other, and this has led to a decreased effectiveness of the movement as a whole.

To understand this better, we need to have a look at the power structures that make up these groups. When we look at the structure of legacy disability organizations at the national and provincial levels we see a few common traits, a hierarchal board structure, members are voted in by other members of the organization. To become a member, you may have to submit a resume and letter of interest, or be in good standing with another organization. There is nothing inherently wrong with this process, but it is vulnerable to biases of power and instutionalization of historical beliefs about structures of power without much consideration for intersecting oppression.

Grassroots disability organizations do not have a very transparent structure. Their membership is not publicly posted as it is with legacy organizations, there’s no staff time, or experience staff changes with new projects. Members have their own vetting system, and much of the communication happens online or is not open to the public. For the Toronto Disability Pride March, our four-person organizing team was vetted by its members based on their past activities and skill set. The advantage grassroots groups have is in the fluidity of their structure, and their nimbleness for dealing with on the ground shifts in the movement. The recognition these groups gain comes primarily out of their collaboration with other groups.

When we look at other movements like Black Lives Matter and Idle No More, and the disruptions they’ve made; these are the types of struggles that legacy organizations were built on. Many legacy disability organizations were built on a history of struggle, and when those struggles succeeded, those projects became government funded organizations who could no longer advocate against their main funder. This has allowed strong disability projects to be co-oped outside of a disability lens.

Consider the case of the Canadians with Disabilities Act, as I discussed in a recent article I wrote called “Trudeau’s Accessible Canada includes Unpaid Work” (Graham, 2017).

Back in 2015, before the Canadian federal election, a movement of disabled people was building across the country. The call for a barrier-free Canada was built in that time by a small, dedicated group of people who reinforced their message daily through social media and on the ground action. Their methods were so effective, that what began as a grassroots call for national solidarity grew into a campaign promise by Trudeau.

What was mandated was more conversation, in the form of a seven month long cross-country consultation process with Canadian with disabilities. Consultations like these are a favored trend in the current federal government. Perhaps this is because they act as public evidence of some kind of action, regardless of how effective it is.

These events were heavily managed conversations. They seemed designed to give the appearance of consent, rather than provide opportunities for consensus and moving forward. At the public consultations, any participant that was given time to speak was restricted to a two-minute limit; a method that was inaccessible for many participants. There was the impression that the people who spoke were expected to be grateful for the opportunity to share their perspective, even when it’s only taken in limited amounts.

There were impressions that a lot of what was being said was being filtered out, and reframed to fit an agenda. Any comments referring to issues of discrimination in immigration, affordable housing, poverty, or anything involving active redistribution was notably left out. There was some potential raised for amending some existing regulations, but little else. The focus was clearly centered on employment, while carefully avoiding much of what keeps most disabled people in poverty.

This isn’t something new of course, in 2001 Michael J. Prince took a look at the state of Disability policy in Canada, and noted something he called deja-vu discourse as a government tactic in working with issues of disability policy. It included strategies like stressing gains made on the surface while overlooking structural gaps, consciously not taking action on particular measures, and promising additional action at some unspecified time in the distant future at which point the whole process would begin again. (Prince, 2004).

So why is this a problem? We are a country that still celebrates advocates that suggest our society would be better if we didn’t see disability. We see this during presentations at International Events like the Toronto Pan-Am Games when Rick Hansen proudly championed “Here in Canada we won’t see your disability” (Graham, 2016) This is also evident in many advertising campaigns where disabled children are framed in battle with their illnesses, or frames people as not disabled because they have other skills (Sick Kids Hospital Foundation, 2016), (Easter Seals, 2017). The dominant narrative is to bring disability into Canadian society rather than having it embraced as part of that society already.

For some of us this may be true, particularly those of us that are white, male, and cis gendered, perhaps these barriers are all they see of disability oppression. For the rest of us, disability is a construct and culture that impacts many aspects of our lives. It’s difficult to have an investment in structural change when working with those who are still invested in that system.

During the consultations I spoke of earlier, instead of reaching out to offer paid work to disabled people, they paid consulting firms to find disabled people to consult with. They were doing market research rather than accepting the expertise of disabled people in designing policies or programs. Disabled people were brought in as volunteers to act as champions, panels and facilitators, and provide unpaid consultation. This is a significant problem, and one that many disabled people are familiar with; recognition of expertise without status or compensation. Volunteers were put in a position of either feeling exploited or declining their knowledge, while government representatives proclaimed the need for more jobs for disabled people within the consultations.

The contrast between our political language around disability and the lived reality is most clearly seen when we can see past our privilege. The Excessive Demand clause in Immigration and Refugee Act is a strong example of this. I have many privileges in my life, but the one I’ve taken is for granted was my citizenship. If I had not been born a citizen of Canada I would not have been able to become one. My disability could be seen as an excessive demand on the health and social services system. This clause also impacts people with disabilities who are already citizens of Canada. As long as this exception is law, then our citizenships remain socially exceptional. It is impossible for Canadians with disabilities to find equitable treatment in this country when that which sets us apart bars other people from obtaining citizenship. We’re still sitting at the separate table.

Being a disabled person has power. Over the years since de-institutionalization, a lot of that power has been eroded by shame, doubt, striving for normalcy, and the idea that disabled people should either go to great lengths to hide this part of themselves or see disability as all that they are. During this time our political, societal, and economic structures have benefited from an invisible contributing force of disabled people. In the margins, we support economic structures though our spending habits and an intricate web of services that maintain the oppression of disabled people. By forgetting our power and hiding ourselves we remain invisible, or at least give society little reason to see us.

Policies and programs alone will not provide the systemic change that grassroots disability organization call for, and legacy organizations work to legislate. Change can only happen when a community recognizes its true power and collaborates with the community’s people live in to create that change.

In closing, I would like to finish this talk with some comments from disability activists I spoke with across the country, some from grassroots and some from legacy organizations. I asked them what they would like to see in creating a stronger disability movement.  Some suggested a greater use of technologies like slate, and conferencing systems, others pointed to a greater diversity of members that’s more representative of the communities we come from, still others pointed to great successes in working with labor, as in the struggle against community mailboxes back in 2015.

In all of these conversations there was a common thread. Grassroots and legacy organizations do see a place for each other, and to collaborate. There is also a realization that the disability community is not yet fully aware of its own power.

Yet that power still exists, as a people, we with disabilities show the world that there is no normal way; conventional ways were created by human beings, and they can be unmade. This is our shared strength. We must keep this torch lit, and visible to all who would challenge it. We can and we will take our power back.

Trudeau’s ‘accessible Canada’ includes unpaid work

Marchers holding signs at the Toronto Disability Pride March
Marchers holding signs at the Toronto Disability Pride March. Featuring Beverly Smith.

Back in 2015, before the Canadian federal election, a movement of disabled people was building across the country. The call for a barrier-free Canada was built in that time by a small, dedicated group of people who reinforced their message daily through social media and on the ground action. Their methods were so effective, that what began as a grassroots call for national solidarity grew into a campaign promise by Trudeau….

Instead of reaching out to offer paid work to disabled people, they paid consulting firms to find disabled people to consult with. They are doing market research rather than accepting the expertise of disabled people in designing policies or programs.

Read the full article I wrote for Socialist.ca.

Have your say on the future of the Canadians with Disabilities Act

The Federal Government will be hosting a public forum to get input from the public on what the promised Canadians with Disabilities Act should include.

where and when this takes place:

When: Wednesday, February 8th, 2017

Time: 4:00 pm to 7:30 pm

Where: Chelsea Hotel Toronto – Churchill Ballroom, 33 Gerrard Street West, Toronto, ON

If you would like to attend this event, you will need to contact the Office for Disability Issues in advance so they can send you a short form with your contact information and accessibility needs.

Pro-Tip: Go with a group and plan the questions you want answered.

Would you like some suggestions of what you might say to the Federal Government at these consultations?

Here are a few starting points from the AODA Alliance.

Here are a few points that I’ve made regarding an Accessible Canada for All.

  • The need for accessible, affordable housing. People can’t be expected to find decent work without decent housing that meets their access needs.
  • Protection of the rights of parents with disabilities.
  • Accessibility in healthcare and all stages of education.
  • Including Indigenous Peoples and refugees in the discussion, and allowing them the same or greater accessibility as the rest of Canada.
  • Police training in effectively and sensitively working with disabled people.
  • Distribution of Health and Social transfers to address the inequities in the systemic barriers that exist between provinces and territories.

This is an opportunity for disabled Canadians to have equitable status as citizens and residents of this country. We need effective enforceable legislation that works for all of us.

Disabled Canadians are more than consumers and potential employees. The Federal legislation must have a broader scope to create equitable rights for disabled people with effective enforcement.

Other ways to Participate:

  • Write to your MP
  • Submit your thoughts to be gathered by SCI Ontario.
  • Participate in the online questionnaire until February 28th, 2017. The questionnaire is also available in an accessible PDF version.
  • Submit your feedback in the language of your choice (English, French, American Sign Language or Langue des signes québécoise) and preferred format such as online, handwritten, video or audio submissions. You can provide your input to the Office for Disability Issues via:

Phone: 1-844-836-8126

TTY: 819-934-6649

Fax: 819-953-4797

Email: accessible-canada@hrsdc.gc.ca

Mail:
Consultation – Accessibility Legislation
c/o Office for Disability Issues
Employment and Social Development Canada
105 Hotel-de-ville St., 1st floor, Bag 62
Gatineau QC K1A 0J9

All of the feedback we receive will be incorporated into reports that will be made available on the consultation website and in alternate formats, on request.

You can also consult the Discussion Guide for more information.

 

Keep Affordable Housing in the Federal Budget

Let’s not let affordable housing be another broken promise from Trudeau.

  • 235,000 Canadians experience homelessness in a year.
  • 1 in 5 renters spend more than half their income on housing.
  • 1.5 million households can’t find decent housing they can afford.
  • The affordability of housing for low-income families living in social and co‑operative housing is uncertain, as federal funding agreements will expire. In the absence of a new federal commitment, by 2020, 175,000 fewer low-income households will be assisted compared to 2010.
  • Indigenous households living in cities and communities experience higher rates of homelessness and are more likely to be living in precarious housing than non-Indigenous Canadians.

In an effort to keep housing on the agenda, Acorn Canada has come up with the following template email that you can copy and paste and send to your Member of Parliament.

How to Find Your MP.

Sample Email:

Subject: We need affordable and livable housing now!

Dear Honorable [YOUR MP],

As a resident of [YOUR CITY] we need the federal government to make affordable and livable housing a major priority in the upcoming budget. The housing situation across the country is a crisis, with hundreds and thousands of people living in sub-standard housing. CMHC reports that about 3.3 million Canadians (about 1.5 million households) are in core housing need at any given time.

Please ensure that resources from every ministry are added to the lump some of money being given to housing. Poor and unaffordable housing affects every aspect of people’s lives from physical to mental health and more.

Thank you,

[YOUR NAME]

Did you email your Member of Parliament? Let us know in the comments below.

Changing the Accessibility Conversation #IDPD 2016

Last night I was out for dinner with my Mom. It was a small space, and it took some time getting a table, so we chatted for a while waiting, and then came in and sat down. It was at this point that something unexpected happened. The young waitress came out with only one menu, hands it to my Mom, and asks if she’ll be ordering for me. There was a split second of stunned silence while my Mom and I processed what just happened before I could say “Excuse me?!”.

The young waitress quickly apologized, and handed me a menu. Later after we ordered our meals, my Mom called the waitress over, and asked her to apologize to her daughter. As inherited as this trait might be, it’s still embarrassing for me when my Mom calls someone out on my behalf, though perhaps not nearly as embarrassing as it was for the waitress.

She did apologize, and explained that she hadn’t interacted with disabled people before. I felt a little empathy towards her at this point, perhaps because I too have been on the receiving end of a Mom Rant, and left her with some disability pointers that I hope she’ll remember. Someone else will be getting an email with the Accessible Customer Service Standard.

If this seems at all shocking for 2016, know that it will likely continue into 2017 as well. Today is the International Day of Persons with Disabilities #IDPD. Disabled people across the world have been bringing attention to issues like this all day, and for decades. I’m protected with a certain amount of privilege that keeps situations like this away from me most of the time, but many people are not.

Fellow blogger Dave Hingsburger recently posted about a disabled man who was finally given agency and the power to make a major decision about his own life at the age of sixty. This is a must read, beautiful post, bring tissue.

As a disabled person, sometimes it seems like this loss of agency is something we have to live with, but it’s not. Loss of agency has much more to do with the system we live in then it does with us as disabled people. I think this is particularly important when we talk about employment, which happens to be part of the theme for this year’s #IDPD.

Let’s face facts, employers would still prefer to hire an able-bodied, neuro-normative person most of the time, especially when that potential employee is white. These are hard times to find jobs for many people, but white, educated, non-disabled people seem a little more entitled to those jobs, and we need to start talking about that with them.

Like this waitress, when you’re just doing your job, sometimes it’s hard to see the people who’ve become invisible in the process. Not unlike the indigenous peoples in Canada whose rights and traditions suddenly become invisible so our Prime Minister can approve a pipeline, create some temporary work for other people, and leave progressing our economy and environment to somebody else.

The bottom line: if we don’t talk about our agency and our rights, and making those things visible, they will be lost to someone else who is louder and more visible then we are.

So please speak out when you can, if not for you, then do it for the many of us who are still not in the conversation today. Start with writing to your MP. Talk about accessibility, talk about a Canadians with Disabilities Act, talk about pipelines. It’s time the conversation shifted.

Accessible Apartment elevators down 3 times this week in Etobicoke

I’ve lived in the same co-op apartment building since the spring of 2010. There have been times over the years when I’ve been frustrated with where I live, but nothing quite like this past week.

I live in a co-op in Ward 6 in Toronto. I’m fortunate to live in a wheelchair accessible apartment that I can afford, although I think the idea that someone should feel fortunate to live in a space that they can afford and access contributes to the kind of complacency leading to the situation that I’m now in.

As I write this, both elevators in my building are down for the third time this week. I live on the eleventh floor, and I have no idea when they’ll be up and running again. To clarify that, one elevator has been down for the entire week, and within this week the other elevator has broken down three times.

The first time was Tuesday, November 22nd, at around 10:30pm. I had just come into the building after visiting my friend in hospital on the other side of the city, so it was already a long day. I was just about to enter the elevator when the fire alarm went off. I waited downstairs for the fire department, and the fire situation was quickly resolved, someone was smoking in the stairwell. That should’ve been the end of it, but it wasn’t.

The firemen couldn’t get the elevator to go back in service. They couldn’t even get inside. They tried everything they could think of to get the elevator running again, even setting the alarm off to try to get it to reset, but it wouldn’t.

At this point I should explain that the building has some security, but they check on a range of building in the area. There is paid maintenance during the weekday, and the rest of the time we rely on volunteer maintenance. It’s well known in my building that the volunteer rarely answers his phone, and you have better luck banging on his door, but he was on vacation. My building manager was also on vacation.

There are a lot of seniors, and people with disabilities living in my building, thankfully I was the only one stuck downstairs. Security contacted my building manager, who contacted the daytime maintenance and the elevator repair company. It was about 11:30-12am when the maintenance guy came, he was not able to fix the elevator. He and security stayed with me until 1 am when my partner could get there. My partner and I decided to leave for an accessible hotel, the closest an hour away. My power chair was nearly dead, my cell phone was dead, and I had just the clothes on my back and my purse.

At 2 am, the fire department, thankfully nearby, saw us waiting for the night bus, and told us elevator repair company had shown up, and we went home. They knew because one of my neighbours got fed up and called 911. My local fire department is actually pretty great.

Since then, it was down Friday November 25th from before 6:30am to 10:30am, and again today, which is Sunday November 27th, I do not expect the elevator to work until Monday. I only found out about this because the person who came to assist me in the morning climbed 11 flights of stairs to get to me.

For me, I work full-time, and this impact my job and well-being. I’m trapped in my own home today, but it’s also a major safety concern for the seniors and people with disabilities that live here. What if an ambulance was called?

I recognize that sometimes things happen, but what really is most upsetting is the lack of preventative measures or concern.

When I called the building office on Friday, they acknowledged the problem, but offered no solutions or preventative measures. She offered to call me when the elevators were up, but I was already downstairs by the time she thought to call.

At the very least, we need full-time maintenance staff, and someone to check on vulnerable people when the elevators are down for more than an hour. Co-op members should be informed of expected repair times, and be given the option to switch companies if that’s what’s needed. This cannot be allowed to continue.

I’m writing to my Councillor Mark Grimes and my building manager Gary McMayo. I welcome other suggestions.

Toronto Area Community Consultations on Electoral Reform

Let’s make sure disabled voices are heard on this important issue!

  • The following is a list of community consultations on electoral reform happening in the Toronto area, please find the consultation closest to you if you wish to attend.
  • There are consultations happening across Canada. Please contact your MP for more information on these consultations.
  • Please Note: Some locations require RSVP.
  • Please also note: At time of writing, no accessibility information is readily available regarding these consultations. I will update as more information is available (all the more reason to make sure disabled people are heard on this issue).

Tuesday, September 6th, 2016 – Electoral Reform Town Hall, Hosted by the Hon. Kirsty Duncan and MP James Maloney. 7 – 9 pm, Etobicoke Civic Centre, 399 The West Mall, Etobicoke, ON

Tuesday, September 6th, 2016 – Willowdale Electoral Reform Town Hall with MP Ali Ehsassi, 7pm – 9pm, North York Civic Centre Council Chambers, North York, ON RSVP

Wednesday, September 7th, 2016 – Electoral Reform Townhall with MP Salma Zahid, 6:00 – 8:00 pm, Scarborough Centre Scarborough Civic Centre, Committee Rooms 1-2, 150 Borough Drive, Scarborough, ON

Thursday, September 8th, 2016 – Electoral Reform Townhall with MP Bill Blair, 6 – 8pm, Warden Hilltop Community Centre 25 Mendelssohn St, Toronto, ON

Sunday September 11th, 2016 – Electoral Reform Townhall with Hon. Carolyn Bennett, 3 – 5 pm, Christ Church Deer Park, 1570 Yonge Street, Toronto, ON

Wednesday September 14th, 2016 – Federal electoral reform community dialogue tour with Minister of Democratic Institutions Maryam Monsef, time and location to be confirmed, Toronto, ON

Wednesday September 14th, 2016 – Electoral Reform Townhall with MPs Jane Philpott and John McCallum, 7:30 pm – 9:00 pm, Markham Village Library Fireside Lounge, 6031 Highway 7, Markham, ON

Wednesday September 14th, 2016 – Community Consultation at 6:30pm at the Calvary Church to discuss and share ideas about the future of Canada’s democratic principles, and to identify and study other voting systems to replace the first-past-the-post. Toronto-Danforth, ON

Sunday September 18th, 2016 – Electoral Reform Town Hall with MP Rob Oliphant, (Special Guest to be announced), 2 – 4 pm, Don Valley West at Temple Emanu-El, 120 Old Colony Rd., Toronto, ON, RSVP

Sunday September 25th, 2016 – Electoral Reform Townhall with MP Francesco Sorbara, 3 – 6 pm, Vellore Village Community Center, Open to all residents of Vaughan-Woodbridge, Woodbridge, ON

Come out for TTC Accessibility for All!

Wednesday, August 31, 2016 at 4:00pm
Please join us at Yonge and Bloor Station, Toronto, Ontario


D!ONNE Renée is the organizer behind this event. If you have any questions, want to throw your virtual support behind her, or have comments, reach out to her via email or on Twitter at @OnElectionDay.

Click to listen to audio announcement.

The announcement reads:

Accessibility is a Right — Not an Option

On Wednesday, August 31, 2016 – Between 4pm – 8pm, on behalf of community and Public interests, an #AccessibilityNow! TTC campaign/protest will take place starting in the Yonge and Bloor area to raise issues concerning discrimination based on disability, barriers, and ableism in transit and its services.

The Accessibility for Ontarians with Disabilities Act sets out the interpretation for “barriers.” Too many barriers exist within the TTC. It is not acceptable to take a “minimum/at least” approach in improving access for all. The standard should be a model that reflects an equal to or greater than the access that is currently available, model. The equal to or greater than the access that is currently available model is a model of equity and equality.

People have a right to access public systems; in this right, people should feel that they have the option to be free to choose whether they access those systems or not. We are all not free just to be.

Approximately 35 out of 65 subway stations are “partially accessible,” on good days. Functioning equipment = good days. “Partially accessible” means that all patrons don’t have the option to access the system for lack of elevators, Braille information and helps, proper signage (large print, clear, large-enough digital boards), functional escalators, inaccessible entrances/exits (now including Presto Card gates and readers) to subway stations, buses, streetcars, and extraordinary Wheel Trans wait/scheduling. Plus the TTC worsened accessibility when they began replacing the names of Toronto’s subway lines with confusing numbers.

TTC (and transit across Ontario and Canada) must be proactive in its operations and provide equality in its services and not discriminate against anyone, including people with disabilities and/or people requiring accessible access in order to use its systems. TTC was able to find money to implement Presto Card systems into its subway, bus, and streetcar services even though the gate systems being used at subway and bus stations are all not accessible; but TTC seems to be unable to be actively proactive in ensuring that all areas of TTC are fully accessible.

While this event will take place in downtown Toronto, the issues and concerns being raised affect all of Ontario and Canada. We want everyone to have the ability to travel independently, or in group, as we so choose.

We want a barrier-free Canada.

Will you help?

Will you join the protest and invite others to do so too? Will you gather with community in accessibility advocacy? #AccessibilityNow #GetItRight #AODA #AODAFail