Article: What Does Disability Justice Mean to Me?

This article was written by Harmony Bongat, and originally appeared in DABC’s Transition magazine on Disability Justice (Spring 2022). Read the issue here.

If you’re interested in contributing to Transition as an individual or an organization, please email transition@disabilityalliancebc.org.  _________________________________________________________

image of the author, harmony bongatI was introduced to Disability Justice through a friend a few years ago. I had just received a diagnosis of fibromyalgia and my visual impairments were worsening, as were my mental health issues.

I was stuck in a medical system that left me feeling hopeless. My circle of non-disabled friends didn’t understand what I was going through. My family minimized my anguish, inundating me with toxic positivity, telling me “I’d get through it” or “I’ll get better.” Everyone around me offered unsolicited advice. I felt confused, scared and lonely — I wasn’t being comforted or supported.

One day, I started attending a group support meeting called Chronically Queer and was introduced to the Disability Justice movement. To me, Disability Justice means: compassion, kindness, resilience and community.

An ableist society says, “You are not welcome.” Disability Justice says, “We want you here.”

Disability Justice understands that, as a disabled, queer, Filipino, solo parent, living in poverty, my experience as a person with a disability is different from the experiences of many other people with disabilities.

Within the medical system, for example, female, queer, people of colour are just not given the same standard of care as white, straight, cisgender men.

I minimize my emotions and mask or hide my queerness. I‘m often asked inappropriate questions or not taken seriously.

And, worst of all, I have no choice but to be entangled within this system. It’s disheartening and exhausting, and wears away at my dignity and self-worth.

But, within the Disability Justice movement, I am given back what the health system and other systems of care have taken away. It sees my lived experience as a wealth of knowledge that I can share knowing it will be valued.

Furthermore, people with disabilities who are not able to “sustain gainful employment” (their words), like myself, must undergo scrutiny in applying for financial assistance. I must show just how disabled I am by divulging details I know will be scrutinized without the compassion and empathy I need–all this, despite having doctors’ diagnoses of chronic conditions I will have for the rest of my life.

People with disabilities know that disability labels come with negative stigma, perpetuated by systems of oppression that all of us are living under. But in a room of people with disabilities, there is joy and comfort and excitement! Other people with disabilities just get it (get US), understand and sympathize. There is an air of excitement and community. We can work together for social change, and, at the same time, talk about everyday life.

We talk about movies where a character with a disability is a well-rounded person, not one that exists for the benefit of someone else. We play board games where everyone can participate, regardless of their level of functioning.

We try to meet everyone’s lighting, seating, scent and sound needs. We offer food or go to restaurants where everyone can eat, regardless of dietary restrictions, paying attention to how much meals cost. We know a lot of us have been through trauma, so we use content and trigger warnings before talking about difficult subjects.

Creating inclusion can be as easy as asking someone if they have what they need and, if they don’t, working with them to see how you can help — and giving that help in a way that doesn’t infantilize, shame or “other” them.

Within the Disability Justice movement, we purposefully engage with others and share what we learn about our conditions, symptom management techniques, self-care treatments, mental health resources and self-advocacy measures.

Disability Justice reminds us to take care of ourselves first. I am reminded that I don’t need to be at the front lines to be part of the movement. I want to know that I can make a difference and that I contribute whatever I can to fight ableism. Just existing each day as a person with a disability means that I’m doing enough.

Right now, one of my contributions is my story. I share it in the hope that it will be listened to and — right now — that is enough.

Chronically Queer is a support group for anyone who is 2SLGBTQIA+?; and who has a disability, chronic condition and/or mental health issue. Come and join us: https://www.canbc.org/queer/chronically-queer/.

Harmony Bongat is a disability justice advocate and educator through Creating Accessible Neighbourhoods (CAN), as well as a researcher of 2SLGBTQIA+ history.

EI Benefits Should Be Exempted from PWD Income

DABC has submitted an advocacy letter addressed to Hon. Nicholas Simons, Minister of Social Development and Poverty Reduction regarding the treatment of EI benefits on PWD income. The Ministry had provided a temporary exemption on EI benefits starting in April 2020 and which ended in November 2021, We feel strongly that EI benefits should be considered earned income that can be treated under the annualized earnings exemption limit rather than clawing back monthly PWD income dollar for dollar as is currently the case. Please read our full advocacy letter here:

https://disabilityalliancebc.org/wp-content/uploads/2022/03/Minister-Simons-DABC-Letter-on-EI-Exemption-for-PWD-Clients.pdf 

Minister Simons - DABC Letter on EI Exemption for PWD Clients

Want to volunteer with DABC? Apply to be a volunteer receptionist!

Graphic that says "We're seeking volunteer receptionists!" in black font, over a watercolour blue rectangle. There is a graphic of a landline phone and the DABC logo is at the top of the page. Disability Alliance BC (DABC) is seeking passionate and motivated volunteers to support our front-desk reception as we work to bring back our advocacy work in-person at our office in downtown Vancouver. DABC is a provincial, cross-disability non-profit, charitable organization that champions issues impacting the lives of people with disabilities through our direct services, community partnerships, advocacy, research and publications. 

Our reception volunteers are often the first face or voice that a client interacts with when connecting with DABC. They exhibit an empathetic and professional attitude and respond to inquiries about our services. DABC provides a variety of services that assist clients with applying for provincial and federal disability benefits, Disability Tax Credit, Registered Disability Savings Plan, tax filings and tax credits, legal aid, and wheelchair accessible housing. Reception volunteers will be trained and mentored on an ongoing basis through regular supervision from the Advocacy Access Administrative Assistant, Advocacy Access Program Manager and the Access RDSP Program Manager. All of our current reception volunteers have lived experience with a disability.  

Our Reception Volunteers: 

  • Respond to client inquiries over the phone, email and in-person 
  • Screen clients for eligibility of our services and conduct intake of client contact information for our waitlists 
  • Keep detailed and accurate records of visitor requests/calls 

Reception Volunteers should have the following skills and qualifications: 

  • Be computer literate and proficient with Microsoft Office software, specifically Excel, Word and Outlook  
  • Have strong verbal and written communication skills and the ability to communicate complex concepts in plain language 
  • Have excellent interpersonal skills and the ability to work effectively with clients and staff across many diverse backgrounds 
  • Be self-motivated, adaptable, and able to work effectively with a team as well as independently 
  • Maintain a professional, respectful and empathetic demeanor with clients and have the ability to manage client expectations as it relates to the capacity and scope of DABC’s services 

The following are strong assets for this position: 

  • Lived experience with disability 
  • Lived experience with provincial disability benefits (PWD/PPMB) 
  • Experience in the non-profit sector 
  • Experience supporting people with disabilities 
  • Knowledge and understanding of community resources available to people with disabilities 

Volunteers will receive a small monthly honourarium for their contribution to DABC’s advocacy work.  

Hours Per Week: 1-2 shifts per week (each shift is 4 hours) 

100% of DABC’s staff and volunteers are fully vaccinated against COVID-19. Many of the clients that DABC serves have medical conditions which make them vulnerable and more susceptible to severe symptoms of COVID-19, and so it is vital that DABC strives to protect our clients from risk of transmission. It is DABC’s policy to request that all volunteers be fully vaccinated.  

 DABC is an open and diverse organization that promotes inclusive hiring practices. We encourage applications from qualified applicants who identify as visible minorities, Indigenous persons, and of all sexual orientations, gender expressions and identities. People with disabilities are especially encouraged to apply. 

To Apply: Please send an email expressing your interest with the subject line “Volunteer Application”, along with a resume to advocacy@disabilityalliancebc.org. No phone calls or faxes please.