people with disabilities during the pandemic

Photo Credit: Disability:IN


“They gave me a pamphlet,” she said, one that was 15 years out of date, and offered no advice on what we were supposed to do next.


I have since met people who share my diagnosis, and I’ve witnessed firsthand how these social connections can help overcome stigma, build friendships, and increase access to support services.

When the COVID-19 pandemic swept the world, people with disabilities told me their support networks stopped meeting in-person, and moved completely online. Despite the constraints of social distancing, they said these virtual communities have been critical sources of comfort and resiliency over the past year.

Learning to thrive

I was diagnosed with dyspraxia when I was four years old.

Also known as developmental coordination disorder, dyspraxia is “a disorganization of information from your body to your brain and back again,” according tooccupational therapist Susan Madigan. It affects your spatial awareness, your sense of time, and your response to your environment. Dyspraxics find it challenging to tie knots, catch a ball, and multitask. They have poor short-term memory, and are hypersensitive to their surroundings.

My only sources of information about this were doctors who often didn’t fully understand my disability. Most of the information I found was either outdated or too negative about people with disabilities.



What I learned in both school and the workplace is that focusing on my strengths enhanced my confidence, and my willingness to talk about my weaknesses.

As a volunteer for disability-community initiatives, I discovered that this is a common issue. Those who were thriving were accepted for who they are. Those who were struggling were not yet adequately supported by their peers, co-workers, and friends.

Care, comfort — and inequality

Community helps build knowledge and a meaningful social network that supports its members through every challenge and accomplishment, and provides comfort in times of need.

Don’t underestimate the power of comfort, which can help address the community’shigh rates of mental-health conditions.

这些条件往往摆脱耻辱d toxic stereotypes.

Public figures with disabilities, for example, may seem carefree, successful and wealthy, which can lead well-intended people to ask: “Why can’t you be more like them?”

These are stereotypes that mask real inequalities: Access to care, an urgent priority for all people with disabilities, is not always available to those who need it most.

A stark example of this is Nick Jonas of the Jonas Brothers. Jonas has type 1 diabetes, and is the spokesperson for an organization calledBeyond Type Onewhich advocates that “anything is possible” with type 1 diabetes.

Yet this attitude is seen by people with the disease as out of touch with reality. As a wealthy individual, Jonas has access to expensive and high-quality diabetes supplies and care.

Meeting a mother whose son died in his mid-twenties from insulin rationing — because he couldn’t afford his insulin — reaffirmed my belief that “anything is possible” is not actually that simple.

Making the connections

我在一个缩放社交聚会上遇到了比利·斯坦利(Billy Stanley),为患有障碍的人遇到了社交聚会。他是英国东南部的居民,创立了支持网络Dyspraxic Help 4 U在2019年。

“I wanted to highlight the help and entitlements people with dyspraxia could access,” he says. “It was something I felt that the community was lacking and needed.”


People with type 1 diabetes also have a strong online presence with#insulin4all. Chapter members advocate regionally for access to insulin and other essential diabetes needs.

Joanne West, a therapist in Canada and a member of anOntario #insulin4all chapter, lives in Toronto,where insulin was first discovered.

At chapter events, she says, locals with type 1 diabetes “discuss challenges with accessing insulin and diabetes supplies,” advocate for easier access and lower costs, plan activities, and share campaign updates.

Stanley and West both said their communities fill the gaps in existing support services.

“Too many diabetes organizations emphasize children and families,” West said, which wasn’t helpful when she was diagnosed as an adult. Gaining a peer group meant she had new social connections, and was also able to connect with people working to lower the costs of insulin and make access easier.

For Stanley, his immersion in dyspraxia social media was a lifeline.

“Meeting people from across the planet who have dyspraxia and need help was important,” he said. “The feedback on social media helped me focus on what made a difference to the lives of dyspraxics.”

While social distancing and the pandemic shift to online community has been painful, it has, ironically, had a number of positive effects on accessibility.

Chloe Alice, known online asDeviant Dyspraxic,runs theDyspraxic Women’s Network并创建神经多样性 - 意识在线内容。她说,数字平台对于残疾人来说是无价的。

“Skype has a live-caption feature which is pretty accurate,” she said. ”It improves accessibility for deaf and hard-of-hearing people.”

With video conferencing, respecting a variety of accommodation needs is a lot easier. In-person meetups limit whom you can reach. According to West of #insulin4all, switching from in-person to virtual was a valuable collaboration opportunity.

“We are now able to meet more easily,” she said. “We have attendance from people from across the province of Ontario and Canada as a whole. Our meetings have expanded our understanding of issues diabetics face across Canada.”


In disability groups, people can be quite shy about admitting they’re going through a tough time. We all need each other’s support, but our memories of not being accepted for who we are never go away.

Anonymity is a lot harder to do in person — but in virtual meetups, you can turn off your camera without judgement.

克里斯塔尔·肖ofDyspraxia AllianceandDyspraxia杂志主持这两个计划的虚拟事件。她认真对待机密性和匿名性。未经您的同意,分享您所说的或从未发生过的事情。随着相机和麦克风的整个时间出现,就像出现在房间里最响亮的人一样有价值。

Trolls and bullies remain an issue, but the best support groups make sure these people are not welcome. The majority of participants and organizers genuinely care about helping people, and they don’t have time or energy for this sort of behaviour.

It’s also important to keep in mind that these groups aren’t one-size-fits-all solutions. Some people with disabilities find online platforms a difficult place to access and get their point across.

然而,比利·斯坦利(Billy Stanley)找到了一个不仅理想的平台,而且比他想象的要舒适得多。

“Before switching to virtual, the idea of video calling would have sent me into cold sweats,” he said, but it turned out online platforms only opened doors. “The conversation changed. We were pooling together to succeed rather than on an individual basis. Followers needed podcasts and fitness workouts to help them through the pandemic.”

Joining a disability meetup may seem intimidating. If that’s the case, Stanley and West are perfect examples of whom you’ll meet.

They both want people who live with their disabilities to have a better quality of life.

Online matters

People with disabilities have a long history of beingtreated inhumanely,改变这种情况的政策是善意的,但并非总是成功。

Employment and education statistics vary worldwide, but on a global scale theunemployment ratefor people with disabilities is high, and残疾学生are more likely to drop out of secondary school.


Online disability communities are safe places where participants help each other find proper accommodations and support, while fighting against societal barriers. These communities have flourished during the pandemic, and will continue to provide hope and support in a world that can often be indifferent to disabled peoples’ rights and best interests.

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Rosemary Richings||

Rosemary Richings是一个自由撰稿人和编辑曾with organizations such as Spot App, Uptimize, E-bay, and Saatva Mattress Company. Rosemary’s writing has been featured on