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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If you don’t know who Dr Molot is, you can read a bio  here and check out the SStP blog post here.
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You can register for the video seminars he speaks of here:
It’s free – you will be sent the link to watch the seminar videos and be informed of upcoming workshops and resources too, but you can unsubscribe at any time.
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Please share this and do look into the work that Dr Molot and EHA Quebec are doing on everyone’s behalf!
Thank you all!

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

Profile Pictures for Awareness Month

These images are available on facebook. Feel free to download the appropriate one and use for Awareness Month, or at least for May 12th Awareness Day!

Profile pics for MCS/ES Awareness Month Support – Choose from the #MCSchallenge profile pic or do the #MaskChallenge OR do both!

Posted by Seriously "Sensitive" to Pollution on Tuesday, May 2, 2017

 

Please join us in letting the world know we exist!
We have important wisdom to share with everyone!

 “Delegitimizing those with ES-MCS, who may be warning us all of the need for toxics reduction, also tends to impede development of practical, precautionary, potentially preventive and cost-saving public health strategies.”

http://www.womenscollegehospital.ca/assets/legacy/wch/pdfs/ESMCSStatusReportJune22011.pdf

MCS Mask Challenge for Family, Friends, and You!

Here’s an easy way for everyone to show some support!

And maybe, just maybe, wearing a mask for an hour or a day will spread some understanding of  why the people who fought for smoke free policies did that instead of expecting all non-smokers to just wear masks always and everywhere.

The Mask Challenge is brought to you by

Memes For Inconvenient Disabilities

Help us make May 2017 the last time that we ever hear or read the words:

“MCS? #NeverHeardOfIt!!”

#MaskChallenge! Do it! Grow #MCSAwareness!

Watch the video and read the transcript below:

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MCS/ES Awareness Month 2017

Here we go again!

MCS Awareness days, weeks, and months, along with government proclamations have been going on since at least 1998!

It has taken a lot of effort from a lot of people over a lot of years, and for some of us, it doesn’t seem to have made a great deal of difference in our daily lives.

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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:

Continue reading

Amelia Needs Us

 

Many of you are familiar with Amelia Hill, either via  my blog,  her blog, from her facebook group,  or from the several articles she has written or appeared in, where you can read about her most challenging circumstances and how she has worked so hard to not only survive them, but to overcome them and to help others who are hidden away going through similar challenges.

Amelia Hill

Amelia’s awesome mom Danija has contacted me to say that Amelia’s health has taken a real turn for the worse, and that she and her family have run out of funds to get her the very limited, specific foods and medical care Amelia urgently needs now.

A friend has started up a fundraiser where there are more details about what has happened and what is needed.

Please contribute if you can. Every little bit will help.

Amelia Hill’s Medical Fund

https://www.gofundme.com/amazingameliahill

If you can’t donate, then please keep Amelia in your hearts and prayers.

We LOVE you Amelia!
♥ ♥ ♥

P.S. I will keep you updated in the comments when I have more news to share.