This Year Has Been Many Things, None of Which Included Slowing Down

It almost seems unfathomable that it’s time to conclude the year. Time has stretched, contracted and twisted in strange ways since March. But the calendar and the empty Christmas tree on Fed Square indicate that indeed, this year is coming to an end. 

What is there left to say that hasn’t been said about 2020, about the global pandemic, bushfires, borders closures, thousands of deaths, the climate crisis? The list of catastrophes is too long to cover. 

During the prolonged lockdowns we have endured, many people have expressed their experience as ‘slowing down’. At first I thought I was just being fashionably late to the party of that reality, but after long weeks it became clear I wasn’t invited. I have not taken up a new hobby, did not catch up on the latest TV series, and certainly did not feel more at ease with myself or the world.

The experience of slowing down is multifaceted, I believe. It often (although not only) comes from childless people who have had stable incomes, healthcare and trust in the systems to keep them safe and well. Even those who relied on the generous Australian government support have attested to a feeling of Netflix & chill amongst the world chaos. (Note: I consider the Australian and/or Victorian government support and healthcare generous as my main comparison points are the Israeli and US systems. None of those two governments could pride themselves on their healthcare, social support systems or handling of the pandemic.)

I remember the moment I knew this year was going to be like no other, and deeply felt my life taking an unpredictable turn. It was a phone call with my mother who told me that her travel agent recommended not to book those tickets to Australia, because of the COVID crisis. Our family plans were shuttered. Since then, with extreme health concerns, lockdowns and border closures, I have been living in the unknown – when would I see my parents and sisters again. Sometimes it feels like an if rather than a when. That uncertainty has been heavy on my chest since last March, to which along the way many more were added. 

Being a parent to a toddler during this time has often left me feeling trapped and exhausted. Long weeks of isolation without childcare and minimal supports (both physical and emotional), has felt like a Sisyphean task rather than any kind of slowing down. Working in mental health – counselling mere centimetres away from my bed, has felt hard and intrusive. Listening to others’ pain and anxiety around this time was harder than usual – with so many fears and agonies shared with my clients. 

Slowing down for me is when my toddler is entertained and I can rest my legs and peacefully chat to another adult. Slowing down is carving out time for self care – whether it’s Pilates, eating out, writing or attending a poetry night. Slowing down is knowing my cleaner comes this week, and using my energy wisely, conserving for the important stuff, like quality time with my family. Slowing down is having my parents visit, spend time with them and enjoy watching them take some educational and caring load off my shoulders. Not being able to access any of those things for long months, almost all year long, hasn’t felt like slowing down. Spending energy I don’t have, parenting non-stop, working from home, dealing with increased physical pain without crucial exercises, coming up with all the educational activities for my child and more, have felt like a race. Missing family, near and far, managing anxiety about everyone’s health and the state of our world, has been exhausting. 

Many people around the world have had much less luck than me, living in countries where social distancing is impossible, healthcare systems are collapsing and/or inaccessible to many, have been forced into poverty and buried their loved ones. Many people did not receive the healthcare they deserved because of their disabilities, skin colour or other discriminatory practices. Many people have been separate from partners and children for long months. Others are still waiting for essential healthcare delayed by the pandemic. 

Slowing down is a privilege many of us haven’t got. For me, this year felt like trying to float in a rough sea – constantly being pushed under, struggling to breathe, with limbs constantly flinging around to keep me afloat. 

To finish this year, I wish all of us a safer 2021 – a year of equality, health, safety and prosperity for all.

Until next time,

Liel K. Bridgford 

A highlight of isolation, when cuddling a bath toy was as much slowing down as it got. [Image description: a portrait of Liel (a white person) sitting in front of a black metal bookcase, cuddling a pink bath toy with her hand and face. She is wearing a grey jumper and brown glasses and is smiling at the camera. Various books are seen in the background.]

How To Give Back This Holiday Season, Without Spending a Cent

Having good intentions isn’t always enough, right? Many people believe accessibility and equality are important, but don’t realise they have a role to play in making those happen – through everyday life choices.

Becoming a better ally to the disability community is something anyone can do. It doesn’t take a huge investment of time, money or effort. It’s not about changing your way of life, dreams or aspirations (unless those involve contributing to the further marginalisation of disabled people). You can give back by carrying some of the weight of an ableist society – through educating yourself, making mindful choices and educating others. It is that simple. 

Let’s start with the basics, in case you’ve missed it. What is ableism? Ableism is the discrimination and marginalisation of people based on incorrect and oppressive systems that abnormalises bodies and minds. Bodies and/or minds that are deemed abnormal are excluded, mistreated, even killed in our societies. From my experience of living in two countries, travelling, connecting and reading – ableism is universal. Ableism is many-years-old and crosses many cultures, although it has distinct characters in differing parts of the world, different classes, races and genders.

As a disability advocate, I carry an advocacy burden. The advocacy burden is the accumulation of time, effort, physical, mental, spiritual, and social energy, as well as financial commitment and risks that I take in order to improve the lives of disabled people. This include everything from running this website, to writing social media posts, to calling out ableist slurs in my social groups, to calling out discriminatory practices at my workplace, and much more. Facing backlash from calling out is also a part of the burden experienced by many advocates I know. It often involves bullying, hate, harassment and gaslighting.

This advocacy burden is heavy on our shoulders. On top of navigating inaccessible spaces, attitudes, advocating for our needs, and dealing with trauma, we also carry the responsibility for change. This should not be the case though. Just like all humans are responsible for gender and race equality, we are all responsible for carrying the burden of an ableist society, and to dismantle ableist systems and ideas.

This holiday season I invite you to carry at least a tiny bit of the advocacy burden, so that we can start the new year a little more equal. Here are a few things you can try this holiday season (and beyond).

Start by educating yourself from disabled people themselves. There are many great resources out there. If you need somewhere to start, go to my socials for ideas. Educate yourself about what it means to live with a disability, what kind of barriers we face every day – in attitudes, physical spaces, the medical system, in our social groups. You can do this through reading own voices books, blogs, articles, essays and social media content. Listen to music written and performed by disabled musicians. Watch movies and series written and/or produced by disabled people. Listen to a podcast hosted by disabled people. Search for disability stories wherever you get entertained.

Think of disability as a regular, common, normal experience, and commit to thinking from this lens when you live, love and work. A tip to remember and priorities this is filling your social media feed with disabled, cool people (like me) who will remind you that accessibility and acceptance are critical. Ask yourself how accessible is your workplace. Advocate for change as needed.

Call out ableism in physical spaces – Think of access when you visit public places. Consider asking about accessibility before your visit any venue – and put your money into accessible venues. When you visit the next coffee shop, restaurant, hotel, caravan park, etc, consider its accessibility. Does it have wide, step-free access? Can a disabled person reach the toilet and open its door easily? Is there a step to get in to the premises or the bathrooms? These are just examples (not an exhaustive list). When you visit obviously-inaccessible spaces, challenge this and invite the owners to make access a priority. You can do this with any of the options below:

I’m wondering why you have a step here rather than a ramp? | I’m curious to know why your toilet is upstairs? | Did you notice you have a step at the entry? Do you know that there are 1 in 5 people in Australia living with disabilities? Making your shop accessible will help you get more customers.

Talk to your family and friends about ableist slurs. Show them my post about ableist slurs if you need a starting point. You can start the conversation with “I read something interesting recently about ableist slurs, do you know what that is? Just like there are racist slurs we know are inappropriate, there are ableist slurs we should think about. I’ll send you a link to read about it.”

Call out ableism in everyday language – calling out slurs is a great start, and you can do this using the following suggestions:

“Did you know that’s actually an ableist slur? I’d appreciate if we can avoid those in respect to the many people living with disabilities.” |“The word ***** is actually a slur. Do you mind using something else instead? You can try ludicrous, unpredictable, ridiculous, absurd, unreal, unbelievable”. |“Did you know the word ****** is actually a slur? Instead you can say silly, ignorant, impulsive, risky, dipshit.”

Make your holiday social media posts accessible – start with an image descriptions for your pics, captions for your video, and high colour contrasts for your text. 

If you have a useful strategy to carry the advocacy burden, feel free to comment below or on my socials (@Lielkbridgford). 

May we all have a happy, accessible and welcoming holiday season. 

Until next time, 

Liel K. Bridgford