Tag Archives: MCS

So You Think We’re Being Difficult When We ask You to Change Products?

Seriously though:

We are not trying to make your life difficult.

We’re just asking you to choose products that don’t disable us.

“Really? Products we can buy in every store disable you?”

Yes! Everyday products and materials can disable us.

There’s actually a lot of info out there that the things that disable us are harming many other people too, just in different ways.

An info dump of links are included below. Take your time and read through them, as you will learn things that will help you protect yourself and your family in the absence of product and material regulations that should exist to protect us.

In many places, it’s also the law to accommodate us
to the point of undue hardship.

“inconvenience, morale, and preferences are not valid considerations in assessing whether an accommodation would cause undue hardship”

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What’s it Like to Have MCS/ES? Part 3: Toast Chaos

MCS/ES (multiple chemical sensitivities / environmental sensitivities)  is a disability recognized by the Canadian and Ontario Human Rights Codes. There are over a million people with doctor diagnosed MCS in Canada, and so many more all around the world.

In the US, the latest prevalence study found that “among the population, 12.8% report medically diagnosed MCS and 25.9% report chemical sensitivity.”

The term ‘sensitivities’ seems to trivialize the condition in many people’s minds.

You may wonder what’s it really like then, if it’s not trivial?

Here’s how Laura J Mac describes it:

Having MCS means never knowing when you can manage something as simple as making toast.

• Can’t stand up due to pain.

• Can’t figure out all the steps involved to make toast. #execfun

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What’s it Like to Have MCS/ES? Part 2: Curbs

MCS/ES (multiple chemical sensitivities / environmental sensitivities)  is a disability recognized by the Canadian and Ontario Human Rights Codes. There are over a million people with doctor diagnosed MCS in Canada, and so many more all around the world.

In the US, the latest prevalence study found that “among the population, 12.8% report medically diagnosed MCS and 25.9% report chemical sensitivity.”

The term ‘sensitivities’ seems to trivialize the condition in many people’s minds.

You may wonder what’s it really like then, if it’s not trivial?

 

 

From Amy RW Marsh:

I just wrote this analogy for a person who needed one in order to understand EI/MCS:

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What’s it Like to Have MCS/ES? Part 1: Arms, Brains, and Legs

MCS/ES (multiple chemical sensitivities / environmental sensitivities)  is a disability recognized by the Canadian and Ontario Human Rights Codes. There are over a million people with doctor diagnosed MCS in Canada, and so many more all around the world.

The term ‘sensitivities’ seems to trivialize the condition in many people’s minds.

You may wonder what’s it really like then, if it’s not trivial?

‘have legs or brain some days but not others’

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What Are Your Wishes for 2019?

Dream big! What would you wish for? Continue reading

Return to Vendor

Get something stinky
as a gift?
Don’t toss it
on the street
or in the trash.
Don’t regift it
to a friend
or enemy.
Don’t donate it
to a charity.
Do send a message
loud and clear!

Now’s the time Continue reading

CBC News Hi-lights Accessibility Barriers to Housing for People With MCS/ES

Severe sensitivity to household chemicals leaves GTA man
homeless for the holidays

Environmental sensitivities have forced Oliver Zhang to move 70 times in 3 years


I hope that someone can offer or help create a safe place for Oliver Zhang to live.

I also hope that something is done soon to ensure safe, affordable, accessible,  non-toxic, mold-free, housing is available for all  the other people who have  MCS/ES (a condition, not disorder) who need safe and accessible housing.

Since finding a safe place to rest one’s head and body is so challenging, even in the best of current circumstances, Oliver Zhang should not be forced to leave the shelter where he is currently residing if it is physically safe enough for him to be there.  He is in crisis.

Forcing people onto the streets creates preventable trauma and mental health problems in addition to the serious challenges that already exist when trying to survive with MCS/ES in a society full of systemic accessibility barriers.

I know of many people who have had to move numerous (even countless) times  in their quest to find housing that doesn’t hurt and disable them. I hear from too many who are in crisis,  seeking accessible housing. I know people who no longer have the energy to keep looking for a needle in a haystack, because each toxic haystack leaves them more and more incapacitated. I know people with MCS/ES who are sleeping in cars and tents, and I have also known more than a few people who weren’t able to find safe housing and are no longer with us.

This is a preventable crisis.

Oliver Zhang and all the other people who are homeless due to the lack of accessible housing for people with MCS/ES, have been put into this position due to systemic neglect (if not deliberate discrimination) and bad policies, not through any fault of their own.

The City of Toronto has known about the critical need for accessible housing for people with MCS/ES since at least 2007, and most likely long before.

In 2008:

“The City of Toronto has launched a consultation process on the development of the City’s ten-year affordable housing plan, known as Housing Opportunities Toronto (“HOT”); and

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