Tag Archives: invisible disabilities

Two Tales: Temporary Quarantine or Long-term Segregation

 

There have been several articles in the news lately about the experiences of people who have been forced to endure quarantine or social isolation due to the coronavirus.

Many other people are worried about having to stay at home for a couple of weeks, without access to their regular activities, because they have never had to think about what it’s like, but some of us (indeed millions around the world) have been forced  to stay confined and isolated, sometimes for most of our lives! Our stories are seldom told, and when they are told, they’re often dismissed as anomalies and quickly forgotten.

 

When I saw the following articles, I felt the need to add a different perspective.

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Dear Quarantined and Socially Distanced

I’m sorry you have to experience this, but am glad that it is just a temporary experience for you and your family. I personally know how difficult it is (times  1000 or more).

Hopefully if you actually do become ill, it will pass quickly and there will be no lasting effects.

It is more than likely that most of you will have all the medical assistance, food, toilet paper, and everything else that you will need to have available to deal with basic creature comforts and needs, so it will be just the habitual and a few social comforts that are temporarily disrupted for you.

Did you know that more than a few people are not as fortunate, and experience this kind of segregation full time, with no vacations, with few, if any of the relatively easily accessible (to most) basic amenities? And they aren’t criminals!

Say what?

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Endangered Human in Jasper

If you are in or near Jasper, Alberta  anytime between February 29 and March 7, please check out Marie LeBlanc’s Endangered Human presentation at  Jasper Community Habitat for the Arts. I have seen some of it, and it’s very powerful.

 

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Attitudinal barriers, fragranced products, and invisible disabilities

Having been housebound for far too many years due to having to avoid exposure  to common, everyday products and materials that disable me, has given me time to observe the world (and sometimes even make a little sense of it).

Still, there are some things that make no sense. With over 404,207 Ontario citizens diagnosed with MCS, and 740,370 with one or more diagnoses of MCS, FM, and/or CFS (ME) (in 2016), why hasn’t the Ontario government done anything about the Task Force recommendation to raise

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Find all 25 reasons why I didn’t come (to your party)

There are those who invite us to celebrations, sometimes year after year, but who also refuse to remove the accessibility barriers so that we can attend.

There are 25 barriers in this photo.
Can you find them all?

Click on the image to enlarge it.

Don’t understand?

Learn more here:

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You Don’t Look … Invisibly Ableist?

 

Having an invisible disability isn’t easy.

How many of us have experienced this?

“You don’t look like you’re sick or disabled”

Says here that every human has a heart
even when we can’t see any evidence of that

Does anyone ever say:

You don’t look hungry“?

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How to Show That Your Disability Accommodation is Disability-Related

via How to Show That Your Disability Accommodation is Disability-Related

 

Lots of great tips at the link for how to write your disability related accommodation requests.

There are many other helpful resources on the How to Get On website too!

How to Show That Your Disability Accommodation
is Disability-Related

https://howtogeton.wordpress.com/how-to-make-sure-your-disability-accommodation-is-disability-related/