Tag Archives: Housing

Endangered Human Art Project: Bringing Awareness to Chemical Sensitivity

WHO Says We Need Fresh Air?!

Guest Post from Marie LeBlanc

Bringing awareness to chemical sensitivity
Marie LeBlanc at the Centennial Concert Hall in Winnipeg. May 12th 2017.

I am an artist  in Winnipeg who lives with multiple chemical sensitivity (MCS) and environmental illness caused by mold exposure. My art has been in relation to multiple chemical sensitivity (MCS)/Environmental Illness (EI) and toxic environments.

“WHO says we need fresh air?!” is a series of quotes from sufferers of Multiple Chemical Sensitivity, Environmental Illness, Mold Exposure, Electrohypersensitivity Syndrome, Lyme Disease and other conditions related to Chronic/Complex Immunological Neurological Diseases.

The art installation was on display during the evening of Fri. May 12, on Multiple Chemical Sensitivity (MCS)/Environmental Sensitivities Awareness Day,  outside the Centennial Concert Hall (with a few quotes displayed on the indoor screens), and is dedicated to my friend Eliana from Mexico.

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An MCS Awareness Visualization

May 12th is International MCS Awareness Day, and May is MCS Awareness Month.  Many people who have MCS also have  MCAS – Mast Cell Activation Syndrome, where chemical and other exposures cause anaphylaxis.

Guest Post from Raven Galarza de Gold

My request for you to visualize:

I’d like to ask each of my friends to sit in a quiet space for just 15 minutes and close your eyes. Breathe and get calm and relaxed.

Now I want you to think of yourself only. Visualize yourself in your body. Once you see or feel you, I want you to see yourself  Continue reading

Why I LOVE Having Environmental “Sensitivities”

Guest post

In all of this I don’t have a permanent place to stay and paid rent to a landlord who won’t fix anything, my apartment insurance cut me off and won’t help with my possessions, my medicare health insurance is not covering the health aspect and my one doctor wants me to see a doctor out of province which is not covered, and my social assistance did not pay me my disability this month, and family does not understand any of this….At this point I have nothing to lose and everything to gain….I AM MOVING FORWARD!

~ Marie LeBlanc, Manitoba, Canada

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Imagine Being Disabled, Confined, and Invisible

Imagine being disabled (as if drugged, dysfunctional, and definitely disbelieved more often than not) from exposures to legally allowed toxic chemicals in everyday products and materials…. or from wireless signals coming from  neighbourhood wifi networks and cell towers…

Now imagine that some of us don’t have to imagine this scenario, because we can feel our brains and bodies being harmed by the exposures just like canaries in the mines did.

Imagine being confined to a safe bubble of a home to avoid disabling exposures, Continue reading

What I Wear In Bad Air :: E.P.

 

2016 E.P.

“I wear this whenever I leave the house, like when taking my child to the park, or walking by people and homes. I had to wear it indoors as well when I lived in an apartment building, because I get sick from exposure to wafting perfume, and dryer vent laundry scents in the air. Even outside it is impossible to avoid these scents blowing in the air and from people walking by.”

~ E.P.

For more info on masks see:

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For Me, MCS Means …

mcs es invisible disability framed“For me, MCS means having to wear a mask when I go out”

MCS Awareness Month Guest Post from Laura J Mac

Multiple Chemical Sensitivity or MCS (also known as Environmental Sensitivities) is a chronic and disabling condition characterized by symptoms from low-level exposures to common chemicals. To put it simply, really common chemical exposures are disabling to some people, even in very small amounts.

ES has been recognized as a disability in Ontario since 2000, and federally (in Canada) since 2007, yet most people, and in fact many medical professionals, have never heard of it.

May is MCS Awareness Month, though I promise you, we are aware of it all year!

Instead of asking others to imagine something so unimaginable, we asked 1500 people with MCS to share what life is like with MCS. These memes are some of the responses.*

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What I Wear In Bad Air :: Lisa M.

 

2016 Lisa M

“At one point I had to sleep in the mask when in a rental unit. There was smoke coming from a surrounding unit and toxicity from finish that was used on the floor. I typically use avoidance, but for situations where that is not completely possible the mask is used to help with some symptoms. One of the biggest issues I deal with is the impact of environmental triggers causing instant inflammation of my eyes. Since the mask does not help with that it has been necessary to wear it with glasses when avoidance is not possible.”

~ Lisa M.

For more info on masks see:

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