International MCS Awareness Day/Week/Month

Happy Multiple Chemical Sensitivity Week!


More from AESSRA on the Better Health Channel:

“People with Multiple Chemical Sensitivity (MCS) get symptoms when exposed to low levels of chemicals such as pesticides, car exhaust, diesel fumes, perfume, aftershave, air freshener, fragrances, washing powders, chlorine, polyester, formaldehyde, plastics, rubber, mothballs, disinfectants, paints, gas, cigarette smoke and wood smoke. Symptoms can include fatigue, asthma, rhinitis, headache, migraine, memory problems, nausea, diarrhoea, dry or sore eyes, joint pain and rashes.

In NSW Department of Health studies, 2.1% of children and 2.9% of adults had been diagnosed with chemical sensitivity. In a South Australian Department of Health study, about 1% of adults had been told by a doctor that they had MCS and 16% reported some chemical hypersensitivity.

The week aims to increase awareness of allergies and sensitivities, particularly chemical sensitivities and Multiple Chemical Sensitivity (MCS).”

More from Amelia Hill:

Imagine if you could no longer just do the things you wanted to do … like see your best-friend get married, go to your niece’s school concert, gather around the family table at Christmas, hug your friends tight or even celebrate your own birthday … all because the perfumed products and washing powder residue on other people’s clothes made you sick, really sick.

What if you could no longer go to the places you needed to go … Like your workplace, the doctor’s surgery, the supermarket, chemist, bank, a public toilet, the houses of family & friends or even your own home, because the common chemicals found there in the air fresheners, pest sprays, cleaning products, building materials & furnishings made you really sick as well.

What if the television, computer, telephone, oven, washing machine or even the heating & cooling was off limits too?

What if, your entire life was turned UPSIDE DOWN and STRIPPED BARE of all the joys, experiences & the people you loved?

Well, for me, like many other people around the Globe, this is what it’s like to live with Multiple Chemical Sensitivity or MCS.

All I ever wanted was to live an amazing life … to travel the world, follow my dreams, have a family of my own. Instead, I’m confined to one bare room most of the time … trying to survive in a world chock-full of chemicals.

May 12 is International MCS Awareness Day

As I sit here, separated from a world that I long to be apart of, and a future, I refuse to give up hope for, I make this humble, yet urgent request. On behalf of MCS suffers everywhere, I appeal to ALL governments and health professionals for recognition, research, much needed treatments, community support and access to public places, workplaces and basic health care like everyone else.

 What can YOU do to make a difference?

  • Reduce or eliminate chemicals in your home, workplace & public spaces.
  • Choose natural materials, fragrance free products & certified organic produce.
  • Donate to a charitable organisation that provides important support & community services to people living with MCS … like

AESSRA in Australia,

RESHELTER in the U.S. &

MCS AWARE in the UK.


Adelaide, South Australia: Today. When countless people around the world mark ‘International Multiple Chemical Sensitivity/MCS Awareness Day’ on May 12, (& for the entire month of May), many will be doing so from the forced confinement of their own home, like 39 year old South Australian MCS sufferer, Amelia Hill, who has been isolated from the outside world due to severe Multiple Chemical Sensitivity (MCS) & Chronic Fatigue Syndrome (CFS) for almost 6 years.

People with Multiple Chemical Sensitivity (MCS) are made sick by exposures to low levels of many common chemicals – such as perfume, pesticides, tobacco smoke, air ‘fresheners’, cleaning products, solvents and VOC’s found in paint, new carpets, building materials. Many of these chemicals at high levels, can make anyone sick, but chemically sensitive people can become extremely ill after exposures to even minute amounts of these substances (1). Chemically sensitive people also frequently react to foods, drugs, electromagnetic fields & wifi technology & fabric treatments added to clothing & bedding.

Symptoms include, but are not limited to, respiratory problems & asthma, fatigue, muscle weakness & pain, headaches, eye & skin irritation as well as anaphylaxis, seizures and other neurological symptoms. Reactions can occur after chemicals are inhaled, ingested, or absorbed through the skin.

Despite recent research showing physiological similarities in those with MCS (2), there is currently no universal diagnostic test or treatment protocol for MCS. Many sufferers report that doctors are still unfamiliar with the condition, describing unmet medical needs, delays in correct diagnosis or treatment for the wrong condition (3, 4).

The isolation imposed by chemical barriers and the lack of community understanding about MCS contribute to the often devastating nature of this illness.

One time fashion designer, magazine stylist & writer, Amelia Hill first became sick with MCS after living in a house treated with termite sprays at age 15 (5). After years of misdiagnosis, her condition deteriorated and she was forced to live in a single ‘Safe Room’, stripped bare of possessions and comforts of everyday life like floor coverings, bedding, heating/cooling, photographs & books etc. She once spent almost 9 months without television, telephone or lighting. Housebound, she has struggled to locate health practitioners willing to consult with her. Last year, in her kitchen, she had a tooth extracted without anaesthetic.

In addition to isolation, discrimination issues for MCS sufferers are also evident. Due to the vast amount of chemicals, air fresheners, perfumed candies, fragrances/aromas released into air conditioner, pesticide sprays & chemical cleaning products found in most public places & the fragranced products like perfume, aftershave, deodorant & hairspray worn by people found there … MCS sufferers are often unable to access basic community resources that most people take for granted .. e.g access to workplaces, places of worship, shopping centres, public libraries, transport, public toilets, movie theatres, parks, schools, offices of doctors, dentists & safe housing.

The Australian Human Rights & Equal Opportunities Commission (HREOC) acknowledges MCS as a disability covered in the Disability Discrimination Act 1992 & clearly includes chemical sensitivity in its document ‘Access to Buildings & Services- Guidelines & Information'(6) .. however, these strategies are rarely implemented & other government recommendations (4) have largely gone unanswered (7, 8).

A national survey of MCS sufferers (9) corroborates this with the following grim statistics:

·Nearly half the respondents were totally disabled, with two thirds unable to access disability and social services.

·61% were unable to access health services.

·96% were unable to access aged care services.

·89% were unable to access allied and respite care.

.Of those who could access health care, 63% said MCS Hospital Guidelines were not implemented.

·Nearly 90% of patients reported living in either a high or medium degree of isolation.

“It is no longer sustainable for the medical community to keep ignoring the size and sweep of this (MCS) epidemic.” says Dr. Martin Pall, a molecular bioscience researcher at Washington State University and author of the book “Explaining ‘Unexplained Illnesses.’ “(10).

“Reports from around the world indicate that chemical sensitivity is a global problem and the numbers seem to be growing.” Dr Ann McCampbell (1).

“Today we are witnessing a unique pattern of illness involving chemically exposed groups in more than a dozen countries” Dr Claudia Miller, Immunologist, Allergist & author of ‘Chemical Exposure: Low Levels High Stakes.’ (11).

“The problem of Multiple Chemical Sensitivities is, in my opinion, a toxic problem which will, over the next decade, affect almost everyone in some way.” Dr Mark Donohoe, Australian Environmental Medicine & MCS specialist.

“It (MCS) emerged with the advent of the chemical industry post World War 2 & appears to be afflicting more & more people. The most effect way to manage the condition, is to create a chemical-free living space and restrict or avoid chemicals in all ways in every day life.” Nicole Bijlsma, Founder of ‘The Australian College of Environmental Studies’ & author of ‘Healthy Homes, Healthy Families.’ (12)

Respondents in government health surveys in both South Australia (16) & New South Wales (17) 16.4 % & 24.6 % respectively, reporting chemical sensitivity and/or adverse health reactions to chemical exposures, highlights not only the urgent need for widespread recognition, but also fragrance-free & VOC- free policies in public places across Australia, like hospitals, nursing homes, schools, public toilets, housing & workplaces etc much like policies implemented in Canada & the US, (18, 19, 20, 21) allowing MCS sufferers to not only continue employment, but to also access essential health care & resources like everyone else in the community.

Despite living in one room for almost 6 years due to MCS, Amelia shares her story in the media (13), on her own website (14), & on social media (15), to raise much needed awareness for this devastating & often misunderstood illness.

Most people who develop MCS were once healthy individuals who tolerated chemical exposures like everyone else, until they had an exposure from which they did not recover (1). “It can happen to anyone,” Amelia says.


(1) Dr Ann McCampbell

(2) ‘Academic & Clinical Perspectives Ontario Centre for Excellence in Environmental Health’ Ontario Ministry of Health, 2013

(3) Canadian Committee Health Survey, 2010
(4) ‘A Scientific Review of Multiple Chemical Sensitivity: Identifying Key Research Needs’ NICNAS, OCSEH, 2010.

(5) “More than 40 studies on MCS across 5 countries including Australia, have shown one of the most common initiators of MCS is exposure to pesticides.” MCS America
(7) ‘Multiple Chemical Sensitivity in the Australian Workplace’ University of Adelaide, 2011.
(8) South Australian Greens Member, Tammy Franks, 2012.

(9) Allergy, Sensitivity and Environmental Health Association of Queensland, in cooperation with the MCS reference group.
(10) Denver Post

(11) Dr Claudia Miller ‘The Compelling Anomaly of Chemical Intolerance’ Pub Med, 2001.
(16) Fitzgerald 2008
(17) Centre for Epidemiology & Research, NSW Dept of Health 2003
(18) Harvard Teaching Hospital

(19) American Lung Association
(20) Canadian Human Rights Commission

(21) MCS America-Fragrance Free Places.

You can visit Amelia’s blog/site here

More from Miriam over at NaturalMamaRamblings:

Thanks to I now know it is because the date was the birthday of Florence Nightingale.

Originally it started out as Awareness Day for Chronic Fatigue Syndrome but it is now an awareness campaign day and week for several inter-related Chronic Immunological and Neurological Diseases (CIND). The diseases included in CIND include Myalgic Encephalomyelitis(ME) Chronic Fatigue Syndrome (CFS), Fibromyalgia (FM), Gulf War Syndrome(GWS), Lyme and Multiple Chemical Sensitivity (MCS).

Different colours are used to represent the different conditions.
Blue – Myalgic Encephalomyelitis (ME) or Chronic Fatigue Syndrome (CFS) sometimes shown as ME/CFS
Purple – Fibromyalgia (FM)
Green – Multiple Chemical Sensitivity (MCS) or Lyme

For links to all the different online happenings in relation to the 23rd annual International CIND Day see the google doc here

Please check out all the relevant happenings and links. Pass them on to family and friends. There is still way too much stigma attached to the conditions and the people that suffer from them. Sadly, we are often treated like the lepers were and often still are treated.

And more from Linda Sepp over at Seriously Sensitive to Pollution:

People all over the industrialized world have been developing Multiple Chemical Sensitivities and Environmental Sensitivities, or Environmental Illnesses. We are exposed to so many petrochemical pollutants, in our air, water, foods, clothes, furnishings, homes, and elsewhere in daily life, substances which are now known to cause many kinds of adverse health effects, and some of us just have the epigenetic disposition to feel the effects faster and more extremely than others who may develop cancer or some other condition many years later.

I know, this is a long post. I hope you’ve enjoyed it.

(Canary Image by Linda Sepp.)

Michellina Van Loder is a Professional Writer, Journalist and Blogger. This is where she shares her tales about trail blazing her way out of the Labyrinth of Chemical Sensitivities and Mould. This is also where you will find the latest Research on related topics.

Interview with Author, Kathryn Treat: Part I

Hi guys, I’m happy to share with you my first published interview: ‘New Beginnings—No Turning Back’, an interview with Kathryn Treat, author of Allergic to Life: My Battle for Survival, Courage and Hope. It appeared in the December issue of  AESSRA’s Sensitivity Matters Magazine. Sadly, as some of you may already know (and I’m sorry to tell you this if you don’t know already), Treat passed away last December from a stroke. I don’t know if it was related to her illness but I do know she courageously battled and came out on top of a chronic health condition that caused her to be chemically sensitive to moulds and other known chemical irritants. And she managed it all exceedingly well. Her life, and the way she lived it, is an inspiration for us all.


Please enjoy (Click on the link to download, or double click the ‘pop out’ arrow on the top right of the image below)!

Download (PDF, 1.05MB)

Stay tuned for part II

Looking to embed a PDF? Try Google Doc Embedder

Michellina Van Loder is a Professional Writer, Journalist and Blogger. This is where she shares her tales about trail blazing her way out of the Labyrinth of Chemical Sensitivities and Mould. This is also where you will find the latest Research on related topics.

My Reviews Are Back (as am I!)

Due to being under the weather for most of this year, I’ve not been reviewing products that I find useful for people living a life sensitive to chemicals. However, I aim to get right back into the sunshine; now that I’ve wiped away my tears. It’s not like I’ve been grateful for much at all, let alone thinking about how I can help others. But that really has changed. Not sure if it was looking at life through the lens of a camera (it’s still a thing, y’all), or the new found confidence I’m experiencing after completing and publishing my first book project, but I do feel mahoosivly grateful for so much lately. So without further verbosity, here, just in case you missed it, is something I’m most enamoured with lately: My Lilla Rose collection of Hair Jewellery.

My Lilla Rose Dragonfly Flexi Clip

My Lilla Rose Dragonfly Flexi Clip

I already did a post on Lilla Rose, and how I think these products are mighty useful for those of us who have problems with hair elastics; besides, they are so gorgeous and pretty that I want this post to link from my blog page too! And, because I’ve not been blogging since January, this year, 2014, it’s not like peeps are going to expect my product reviews to be back up. But just so you know, I’ve got a review coming up on a Dehumidifier that I’ve been using, as well. And an Australian brand of Mutalfor (as apposed to the type that comes from overseas) that I’ve had great success in using!

Other posts coming up:

The Day I Fell in Love with a Font

Losing Someone to MCS (and how to cope)

The new treatment I’ve been doing for the last year

A post on the Amazing Amelia Hill

Probably some more rabbit tails tales

Housing (mine)

My Latest Trip to the Dentist

And some other topics not usually spoken about…

And, here is something I am mahoosivly excited about: my interview that I spoke about, here, has just been accepted by  AESSRA‘s (AESSRA stands for the Allergy and Environmental Sensitivity Support and Research Association Inc), editor of Sensitivity Matters. Woot woot! In that last post, I asked people to guess who I had interviewed, no one did, but I guess it was kind of obvious anyway because that’s who I was talking about when I alluded to my interviewee; well, it’s our own Kathryn Treat, author of Allergic To Life: My Battle for Survival, Courage and Hope. She’s so amazing, and a beacon of hope to us all! I can’t wait to see this interview come out in print, and I’ll be sure to put a copy of it up here.

And, in case you are wondering if I’ve lost my mind and started to invent my own English language, no (well, maybe I have lost my mind), but I’m not making up new words: Mahoosvie is just one of the latest additions to the Oxford Dictionary.

More from the Sydney Morning Herald:

“The addition this week of ‘mahoosive’ to the Oxford Dictionaries – among a record crop of 1000 other words or terms – flags that it’s considered a perfectly fine descriptor by the boffins who shape the English language.

Once, huge was entirely adequate. But in this age of exaggeration and who-can-shout-loudest, even superlatives such as gigantic, enormous and massive clearly no longer cut it. So we now have a portmanteau (two words thrust together) that combines ‘massive’ with ‘huge’.”

Michellina Van Loder is a Professional Writer, Journalist and Blogger. This is where she shares her tales about trail blazing her way out of the Labyrinth of Chemical Sensitivities and Mould. This is also where you will find the latest Research on related topics.

Information, products and views presented by guest bloggers @The Labyrinth are not necessarily the same as those held by this blog's author, Michellina van Loder. Reviews are my own personal opinions (unless stated otherwise); and satire is used throughout personal posts. Any health topics discussed are not to be taken as medical advice. Seek out medical attention if needed and do your own research; however, you're welcome to use mine as a start.
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