Tag Archives: fibromyalgia

Choices… We Always Have Some

When Toxics Drift

we end up with choices.

Sit outside for a little while to get some Vitamin D

or

Be able to think, wash dishes, and/or make something to eat

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Open Letter to the Ontario Minister of Health and the MOHLTC

Dear Minister of Health, we’re ready for action!

According to official statistics:

250,000 Ontarians had been diagnosed with MCS in 2014
and the discrimination is still systemic in 2018

SUBJECT: Accommodation for People with Disabilities

Honourable Helena Jaczek, Minister of Health (at hjaczek.mpp@liberal.ola.org )


On September 29, 2017,
Ontario  quietly released the report “Time for Leadership: Recognizing and Improving Care”  for those with myalgic encephalomyelitis /chronic fatigue syndrome, fibromyalgia, and environmental sensitivities /multiple chemical sensitivity  (ME/CFS, FM and ES/MCS). This report  was produced by the Task Force on Environmental Health for the Ministry of Health and Long Term Care.

The report found that throughout the Ontario health care system and in society at large, there is:

• a lack of recognition of the seriousness and severity of these conditions
• a profound shortage of knowledgeable care providers
• a dearth of clinical tools to support and guide care
• a discouraging shortage of services and supports for people living with these conditions
• an absence of support for family caregivers

The lack of knowledge and appropriate accessible care has devastating effects on Ontarians struggling with ME/CFS, FM and ES/MCS.

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Corporate Gaslighting and Conflicts of Interest at the Women’s College Hospital

I saw something that shocked me, and I don’t know how anyone involved with this could have thought it was a good idea.

This is what I saw

If you are a Canadian, you will probably understand.

.

It’s pretty much the same thing as this (slightly revised) image:

(pretend it’s done all the way)

What would you think if you saw that?

Shoppers Drug Mart is the antithesis of scent or fragrance free!

 

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Province of Ontario Interim Report on ME/CFS, FM, and MCS/ES

The Province of Ontario’s Ministry of Health and Long Term Care’s long awaited Environmental Health Task Force Interim Report has finally been released!

“We found that, throughout the health care system and in society at large, there is:

•a lack of recognition of the seriousness and severity of these conditions
•a profound shortage of knowledgeable care providers
•a dearth of clinical tools to support and guide care
•a discouraging shortage of services and supports for people living with these conditions
•an absence of support for family caregivers.

The lack of knowledge and appropriate accessible care has devastating effects on Ontarians struggling with ME/CFS, FM and ES/MCS.

For those living with ME/CFS, FM and ES/MCS, the lack of recognition of these serious and debilitating conditions is as harmful as the lack of treatments. …

We urge the Minister to act now to raise awareness of these conditions and address the barriers that keep people with ME/CFS, FM and ES/MCS from getting the care and services they need.”

From the press release:

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Published: “Invisible Barriers, Invisible Disabilities, Invisible People”

My article “Invisible Barriers, Invisible Disabilities, Invisible People”   is now available to read in the

Special Issue on Ecopsychology and Environmental Sensitivities:
Chemical, Electrical, and Beyond

All the articles in the entire special issue will be available for free until Sept. 5  2017, which is unprecedented access!

Please check them out and share as widely as possible!

 

Table of Contents:

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Dr Molot Urges Everyone to Support the Canaries

Please take a minute and eleven seconds  to watch this video from Dr.  John Molot where he talks about MCS (multiple chemical sensitivities) and how we (the people who developed MCS) have been stigmatized and that we really are canaries. He speaks about some of the other serious health problems the chemicals that disable us are causing in those who do not have MCS.
 .

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MCS/ES Awareness Day Projects: Request for Submissions

Marie Leblanc, an artist from Winnipeg who is living with MCS/ES herself, is compiling information and statements to put into an MCS awareness project. There are two  ideas  to contribute to.

The easier one is to share  shorter personal statements about your life with MCS/ES and related environmentally linked health conditions,  which will be projected onto walls in a way similar to the photo below.

 

The other project involves answering 6 questions:

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