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Chemical Exposures, Sensitization, Provocation and Symptom Profiles in Adults with Multiple Chemical Sensitivity: A Cross-Sectional Survey

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10 July 2026

Posted:

14 July 2026

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Abstract
Multiple Chemical Sensitivity (MCS) is a chronic condition characterized by adverse reactions on exposure to low-level environmental chemical exposures, often resulting in multisystem symptoms triggered by substances such as volatile organic compounds (VOCs) from fragranced personal and household products. The condition emerges as public health and accessibility issues, as people with MCS may face barriers to accessing workplaces, healthcare settings, educational institutions, and other public environments. This study aims to describe the chemical exposures associated with the onset of the condition (sensitization) and subsequent symptom provocation in MCS, and to characterize symptom patterns and links with known transient receptor potential (TRP) receptor sensitization models. A cross-sectional survey was administered to Canadian residents aged 18 years or older, living with MCS for at least 1 year, with 18 questions assessing exposure history and associations with onset of MCS and symptom provocation. A total of 119 participants completed the survey. Condition onset often occurred at home (35%) and/or in the workplace (55%), following ongoing exposures (61%). Scents, such as perfumes and/or essential oils, including scented air fresheners, cleaning products, construction materials, disinfectants, and laundry products, were associated with both onset and subsequent symptom triggering. Symptoms involved multiple organ systems, with nearly one-third of participants reporting 11 or more symptoms. Cognitive and respiratory symptoms were most prevalent. Third-hand exposure may represent an underrecognized exposure pathway.
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1. Introduction

Multiple chemical sensitivity (MCS), also known as Fragrance Sensitivity, Chemical Intolerance, or Toxicant-Induced Loss of Tolerance [1,2], is a chronic condition characterized by provocation of multisystem symptoms upon exposure to everyday low-level chemical pollutants, including VOCs emitted from fragranced personal care and household products [3]. The health effects include a wide range of symptoms, such as migraines, dizziness, nausea, and breathing difficulties [4], which recur reproducibly following exposure and typically improve or resolve when the trigger is removed from the environment [5,6]. The duration is usually minutes to hours but can last much longer [7]. In this study, the term “trigger” refers to a chemical substance that elicits symptoms upon exposure, at levels previously tolerated prior to the onset of MCS and tolerated by others. Common MCS triggers include VOC-emitting products such as scented laundry products and cleaning supplies, as well as pesticides, smoke, exhaust, renovation materials, and paint.
The ubiquitous presence of VOC sources in built environments (workplaces, healthcare facilities, residences) raises significant public health concerns, as exposure becomes nearly unavoidable. Hence, individuals with MCS frequently report challenges remaining in or re-entering public spaces due to exposure-related symptom exacerbation [8].
With the condition increasing in prevalence in both the United States and Canada [9,10,11], and recent Statistics Canada Canadian Community Health Survey (CCHS) data indicating that Multiple Chemical Sensitivity (MCS) is a significant and growing public health issue, understanding and characterizing its triggers, as well as its mechanisms, is essential for informing prevention, exposure reduction, accommodation strategies, and public policy. Preliminary 2025 Statistics Canada data suggest that approximately 3.1 million Canadian adults (9.4%) reported MCS, while approximately 900,100 adults (2.7%) reported a medical diagnosis [12]. These findings indicate that the population affected by MCS may be substantially larger than diagnosis-based estimates alone suggest and underscore the importance of understanding environmental exposures associated with symptom onset and provocation, as well as the broader implications for healthcare, accessibility, and public health planning.
Recent advances identifying potential mechanisms and biomarkers [13] provide key evidence that MCS onset may be initiated through upregulation and sensitization of chemosensitive transient receptor potential (TRP) receptors following exposures to agonists (such as certain chemicals/VOCs or inflammatory mediators), as well as by oxidative stress. The onset of the condition is often reported to be associated with high-dose chemical exposure of short duration [14]. Symptom expression repeatedly occurs when exposed to a broader range of structurally unrelated chemicals at lower levels, previously tolerated by affected individuals and typically tolerated by the general population [5,6,15].
While current epidemiological studies have focused on prevalence or symptom burden [11], relatively few have examined environmental conditions at onset or the specific chemical exposures associated with subsequent symptom provocation. This study aims to contribute to and extend the growing body of literature by quantifying both direct and indirect chemical exposures and contextualizing findings within TRP receptor sensitization models. From an occupational health and accessibility perspective, these findings will also serve as a baseline for understanding barriers to healthcare access [16] and accommodation needs in home and workplace settings.

2. Materials and Methods

An online cross-sectional survey was conducted. The survey was created by the research team, consisting of specialist physicians, expert scientists, and people with lived experience of MCS. To ensure content validity, the survey was reviewed and pilot-tested before the study began, with input from people experiencing MCS and a panel of clinicians. Participants accessed the survey via an open link on the Qualtrics XM platform (Qualtrics, LLC), a secure web-based data collection survey tool. Those unable to access the online survey were offered to complete it by telephone, conducted by trained staff.
This study was reviewed and approved by the Women’s College Hospital Research Ethics Board (Protocol # 2020-0157-E). Participants were treated in accordance with the principles outlined in the Declaration of Helsinki. All participants provided informed consent electronically. To maintain confidentiality, participant data were de-identified (identified only by an ID number in all databases).
Recruitment and data collection occurred during the COVID-19 pandemic, specifically between January 19 and February 12, 2021. Participants were recruited via 2 websites (Association pour la santé environnementale du Québec—Environmental Health Association of Québec [ASEQ-EHAQ] and the Environmental Health Clinic, at Women’s College Hospital, Toronto, Canada), on social media platforms (Facebook, Twitter, Instagram) and via email through the ASEQ-EHAQ mailing list.
The target population consisted of Canadian residents aged 18 years or over, proficient in either English or French, who had experienced MCS symptoms for at least one year prior to March 11, 2020. If eligible, and upon consent, participants were directed to the main questionnaire, which included 81 questions, of which 18 (relevant to this paper) were analyzed. The extracted questions delve into (i) exposures linked to the onset of the condition, (ii) the symptom profiles linked to subsequent exposures, (iii) indirect exposures through scents transferred on others and items, and (iv) the unsafe housing prevalence. As the study was conducted during the COVID-19 pandemic, selected questions also assessed the effectiveness of masks designed to protect against infection, as protective measures to reduce exposure-related symptoms.
For the purpose of this study, the word “scent” refers to perfumes, fragrances, colognes, and/or essential oils. Third-hand exposure is defined here as exposure to chemical residues left by a previous use of a triggering chemical (e.g., fragrances, smoke, exhaust).
Data analysis was conducted using SPSS v.28. All data were cleaned prior to analysis. Quantitative data from survey responses were summarized using descriptive statistics (frequencies and percentages) to describe participant characteristics, onset environments, initiating exposures, triggering exposures, unsafe housing conditions, and symptom profiles. Some survey items contained missing responses and were treated as N/A. Percentages were hence calculated based on the number of valid responses for each item.

3. Results

3.1. Participant Characteristics

Of the 119 respondents, 103 (87%) were female. The largest age group was 55-64 years (n=43, 36%). Most participants held a university degree (n=68, 57%) or a college degree (n=40, 34%) (Table 1).

3.2. Onset of MCS

Most respondents (n = 108, 91%) reported that MCS began in everyday environments. Workplaces were the most frequently reported location of onset (n = 66, 55%), followed by the home (n = 42, 35%) (Table 2).
More than half (n=72, 61%) indicated ongoing multiple exposures over a period of time as the main factor associated with onset of the condition (Table 3). Other participants attributed the onset to a series of significant exposures (n=36, 30%) or a single large exposure event (n=20, 17%).
Among participants who reported workplace onset (N=66) , scented air fresheners were the most frequently reported exposures associated with onset (n=30, 45%) (Table 4). This is followed by exposure to scents (n=29, 44%), and to industrial cleaning products (n=24, 36%). Other workplace exposures reported to have initiated the condition include construction or renovation materials (n=22,33%), mould spores/water-damaged buildings (n=20, 30%), disinfectants or soaps (n=20, 30%), paint (n=17, 26%), furniture or carpeting (n=16, 24%), pesticides or insecticides (n=15, 23%), photocopier emissions (n=15, 23%), and diesel or vehicle exhaust (21%).

3.3. Exposures to Disinfectants/Soaps and Reported Symptoms Despite Wearing Masks

Among the 119 participants, 112 participants (94%) reported experiencing symptoms upon breathing emissions from scented disinfectants, and 64 (54%) upon inhaling unscented disinfectants, despite wearing masks. Similarly, for soaps, 107 participants (90%) reported experiencing symptoms upon inhaling scented soaps, and 23 participants (19%) upon inhaling unscented soaps, despite mask use (Table 6).
On exposure to scented disinfectants, the most commonly reported symptoms were headaches (n=84, 71%), brain fog or concentration difficulties (n=78, 66%), fatigue (n=73, 61%), breathing difficulties (n=75, 63%), irritability (n=72, 61%), and coughing (n=65, 55%). Symptom distribution was similar for scented soaps, with headaches (n=78, 66%), brain fog (n=75, 63%), fatigue (n=65, 55%), breathing difficulties (n=72, 61%), and irritability (n=70, 59%) (Table 7).

3.4. Infiltration of Triggers into the Home Environment

Participants furthermore reported exposure to triggers entering their living environment from external sources. Emissions from laundry products were the most frequently selected triggers (n=85, 71%). This is followed by scents (n=76, 64%), disinfectants/sanitizers (n=70, 59%) and cleaning products (n=67, 56%) (Table 8).
Among the top chemical exposures entering the home environment (laundry products, scents, disinfectants, and cleaning products), scents were identified by 41 participants (37%) as triggering the largest number of symptoms (11-19). This is followed by cleaning products (n=42, 35%), disinfectants/sanitizers (n=37, 31%), and laundry products (n=34, 29%). Most participants (29-37%) reported between 11-19 symptoms, while a smaller proportion (24-33%) reported 6–10 symptoms or 1–5 symptom ranges (18-30%).
Table 9. Number of symptoms experienced per exposure.
Table 9. Number of symptoms experienced per exposure.
Most common exposures entering the lived environment Number of participants reporting 11–19 symptoms
n (%)
Number of participants reporting 6–10 symptoms
n (%)
Number of participants reporting 1–5 symptoms
n (%)
Number of participants who did not answer
n (%)
Scents (perfume, cologne) 41 (37%) 30 (27%) 33 (30%) 7 (6%)
Cleaning products 42 (35%) 39 (33%) 21 (18%) 17 (14%)
Disinfectants/sanitizers 37 (31%) 32 (27%) 31 (26%) 19 (16%)
Laundry products 34 (29%) 29 (24%) 31 (26%) 25 (21%)
Upon exposure to the above triggers, the most commonly reported symptoms included brain fog (59–69%), headaches (56–68%), fatigue (59–68%), breathing difficulties (60–64%), and irritability (50–61%). Other frequently reported symptoms were memory difficulties (45–56%), dizziness (45–54%), and coughing (46–56%) (Table 10).

3.5. Housing

Eighteen participants (15%) reported unstable housing (including being homeless, moving frequently or living in a vehicle, tent, or with friends and family (Table 11). More than half of participants (n=62, 52%) reported living in unsafe housing, defined as residential units contaminated with mould, emissions from materials such as new paint, renovations, fragranced cleaning products, and/or infiltration of triggers from neighbouring units.

3.6. Indirect/Third-Hand Exposures

Third-hand exposure to disinfectants refers to contact with chemical residues that persist on items that were exposed to a pollutant source (e.g., tobacco smoke) or were handled by a person using fragranced products or disinfectants/sanitizers. Among the 110 participants who answered questions on indirect exposures, 74% (n=81) reported experiencing symptoms from scents on people/items during assisted shopping (situations in which participants relied on another person to shop for their essential needs). Among the 81 participants reporting symptoms, 53% (n=43) reported severity as severe and 42% (n=34) reported as moderate.
When asked about the actions taken for items with transferred scents, more than half of participants reported having to remove the packaging of the item (n=61, 68%), place the items outside to off-gas the scent (n=55, 61%), or dispose of them altogether (n=41, 46%) (Table 12).

4. Discussion

This study provides an overview of the context and exposure patterns associated with the onset and subsequent triggering of symptoms in MCS.
Survey results revealed several key patterns worth highlighting: (i) MCS onset often occurs in everyday environments associated with ubiquitous chronic or repeated low-level exposures, or from single higher exposure events; (ii) fragranced and cleaning product exposures were frequently identified at both onset of the condition and as subsequent triggers of symptoms; (iii) symptoms involve multiple organ systems, with cognitive and respiratory symptoms most frequently reported, which is consistent with the literature [4,38]; (iv) unsafe housing conditions (exposure to symptom triggers from neighbours, renovation materials, or paint) is a potential compounding factor leading to homelessness; and (v) third-hand exposure may be an underrecognized yet prevalent trigger.

4.1. Initiation Patterns, Onset, and Initial Receptor Sensitization

In this study, the vast majority of participants (91%) attributed the onset of MCS to workplace or home environments, highlighting that MCS is more likely to be initiated in non-industrial, non-catastrophic contexts, consistent with the literature [17]. Furthermore, the observation that 61% of participants reported sensitization from ongoing exposure over time highlights repeated low-level exposure to everyday chemicals in the home or workplace (e.g., the routine use of fragranced cleaners, air fresheners, etc.) as a risk factor for developing MCS [18]. Survey responses also highlighted that fragranced consumer products (such as perfumes, air fresheners, cleaning products, and laundry detergents) in the home were frequently associated with the onset of the condition, followed by exposures to construction/renovation activities and pesticides. This is mirrored in workplace exposures, where respondents identified the presence of air fresheners and industrial cleaning products as the main exposures associated with the onset of MCS.
This trend is observed in several other reviews. In Caress and Steinemann [19], respondents reported that their original hypersensitivity was produced by exposure to pesticides (27.5%), solvents (27.5%), new construction/building materials (17.4%), and gasoline or other petroleum products (15.9%). Miller [1] identified two broad classes of MCS initiators: synthetic organic chemical derivatives (VOCs and pesticides) and biogenic toxicants (e.g., mould). In Masri et al. [14], the category of mixed VOCs and semi-volatile organic compounds (SVOCs) was the most prevalent exposure implicated in potential MCS initiation across exposure events, followed by pesticides and combustion products. In Hojo et al. [20], exposure to indoor air contaminants such as renovations (63.2%) and pesticides (27.4%) was also identified as an onset factor for the condition.
Cumulatively, our findings are consistent with the transient receptor potential vanilloid 1 (TRPV1) and ankyrin 1 (TRPA1) receptor sensitization models [6], whereby initial significant or chronic exposures to everyday pollutant sources are believed to sensitize the individual through TRP sensitization, thereby lowering their chemical tolerance threshold over time. Furthermore, in line with our findings, the models highlight synthetic organic chemicals (e.g., VOCs from fragranced and cleaning products, renovation materials, pesticides) and biogenic toxicants (e.g., mould) as the two broad classes of initiators.
In Claeson and Andersson [21], for example, masked exposure to acrolein, a TRPA1 agonist, elicited symptom responses in individuals with MCS, suggesting TRPA1-mediated sensory sensitization. TRPA1 is the most broadly tuned chemosensory channel known [22], and acrolein is a ubiquitous VOC formed during incomplete combustion of gasoline and oil, tobacco smoke, and reactions between ozone and components of indoor air [23,24,25]. Past animal studies also highlighted behavioural and neurochemical sensitization from repeated exposures to solvents and aldehydes (including toluene and formaldehyde, often emitted from cleaning products, renovation materials, etc.) [26,27,28].

4.2. The Spreading Phenomenon

Receptor sensitization is then followed by a “spreading phenomenon”, whereby the chemical intolerance widens to include a larger range of diverse chemicals and a lower tolerance threshold. This phenomenon refers to the well-documented clinical observation that sensitivity initially confined to one chemical irritant or mixture expands over time to encompass multiple, chemically unrelated exposures. This occurs because, once sensitized, TRPV1 and TRPA1 are more easily sensitized to other agonists [29,30,31], as explained by established sensitization mechanisms [32,33,34,35,36]. In other words, sensitized individuals will react to significantly lower concentrations of a larger set of unrelated chemicals [1].
This is illustrated in participant responses. The same categories of exposures that contributed to the onset of the condition remain primary symptom triggers: scents, cleaning, laundry, and disinfectants. Furthermore, participants also reported reacting to triggers from external sources (e.g., laundry emissions infiltrating their home environment or neighbourhood).
According to Gibson and Vogel [37], once MCS has developed, primary symptom triggers include pesticides, formaldehyde, fresh paint, perfume, and air fresheners. Findings were further supported by Steinemann [9], who found that 67.6% of participants identified air fresheners and deodorizers as triggering health problems, 57.9% identified scented laundry products coming from dryer vents, and 67.6% identified being in a room cleaned with scented products as a trigger.
Additionally, our findings reveal that nearly three-quarters of the participants (74%) identified third-hand exposures as a symptom-triggering factor. This finding, which does not appear to be quantified in the literature, potentially highlights an emerging challenge for individuals with MCS and an under-recognized exposure pathway.
The increased use of disinfectants and sanitizers during the COVID-19 pandemic appears to have introduced a new layer of risk, with 44% of participants reporting disinfectants as symptom-triggering, 96% of whom reported symptoms upon inhalation.

4.3. Symptom Profiles

Survey results reveal a significant symptom load, involving multiple organ systems, with cognitive and respiratory symptoms dominating.
A notable first trend is indeed the high proportion of participants reporting 11–19 symptoms upon exposure to triggers (e.g., 35% of participants reported 11–19 symptoms upon exposure to cleaning products). This is also the case for scents and fragrances, where 37% of participants reported 11–19 symptoms, and for laundry products, where 29% of participants reported 11–19 symptoms. The wide range of reported symptoms (from respiratory to dermatologic and gastrointestinal) furthermore highlights the involvement of multiple organ systems and is consistent with the most commonly used case criteria for the diagnosis of MCS [39,40,41]. This high and diverse symptom load is similarly observed in Saito et al. [42], where nearly 17 symptoms were identified, and in Fares-Medina et al. [41], where more than half of female participants (59%) reported two or more symptoms (from musculoskeletal to genitourinary). In Hausteiner et al. [43], more than a third of participants reported five or more symptoms.
Reported symptoms fell into two main categories: cognitive and respiratory. Cognitive impairments included brain fog, memory difficulties, and irritability (affecting 45–69% of participants across various triggers). Respiratory symptoms included breathing difficulties and coughing (46–64%). The prevalence of cognitive and respiratory symptoms has also been well documented in recent studies. In a study by Fares-Medina et al. [42], airway and mucous membrane alterations were often the first symptoms that manifested (68.9% of participants). Del Casale et al. [4] reported similar trends with a high prevalence of respiratory and neurocognitive symptoms. In a case study by Guerrero et al. [44], symptoms were similarly categorized into two main groups: respiratory (52% of cases) and neurological (29%). These trends were similarly observed in a study by Steinemann [9], in which the most commonly reported symptoms were respiratory difficulties (50.3% of respondents) and migraine or headaches (46.9%).

4.4. Limitations and Future Research

This study contains some limitations worth noting. First, the findings rely on self-reported data, which often requires recalling the context and nature of exposures that led to the onset of their condition. Self-reporting can be subject to recall bias and inaccuracies. Secondly, voluntary participation may have additionally introduced self-selection bias into the sample. Furthermore, although the inclusion criteria ensured that participants had lived with MCS for at least a year, the study did not require clinical confirmation of diagnosis. However, due to documented difficulties in obtaining a formal diagnosis [16], reliance on self-identification appeared as the most feasible option. Finally, the findings are specific to the Canadian context; therefore, although similarities were found in other studies, our findings may not be directly generalizable to populations in other countries with different exposure types.. Despite these limitations, this paper adds to an under-researched area on MCS, by quantifying exposure patterns (locations, sources) involved in the onset and subsequent triggering of symptoms. Future research expanding the body of knowledge on third-hand exposures is recommended (e.g., quantifying chemical residues or assessing the economic burden of disposing of contaminated items). Furthermore, as data collection occurred during the COVID-19 pandemic, a repeated cross-sectional survey would allow comparison of exposure patterns and symptom profiles during and after the pandemic. Finally, given that the next epidemic cannot be predicted, it is recommended that research be conducted proactively to ensure that disinfectant products are fragrance-free, have the lowest VOC emissions, and are tested for human and environmental health.

5. Conclusions

This study provides a detailed description of environmental exposures at the onset of MCS and during subsequent triggering of symptoms. Delving into the circumstances of sensitization and symptom triggers, the survey findings are consistent with TRPV1 and TRPA1 receptor sensitization models, highlighting repeated low-level exposure to everyday chemicals (particularly those in fragrances and cleaning products) as key drivers of both sensitization and triggering stages. Notably, the results highlight indirect or third-hand exposures as an under-recognized exposure pathway leading to real-life consequences, such as the disposal of recently purchased contaminated household items (including food), thereby adding an additional economic burden.
The findings furthermore underscore the breadth and severity of symptom burden, with more than a third of participants experiencing 11 or more symptoms on exposure to triggers. Although cognitive and respiratory symptoms were most common, the extent of symptom categories highlights the involvement of multiple organ systems, which vary significantly from one individual to another.
This heterogeneity (in trigger source, symptom type, and severity) creates several significant barriers in healthcare, including obtaining a formal diagnosis, further compounded by limited medical training. Whereas a formal medical diagnosis is required for accommodation, limited knowledge among medical providers of the condition results in a lack of support for accommodation and inclusion in all spheres of accessibility (including workplace, housing, and healthcare). Addressing this challenge, therefore, necessitates targeted responses. Though tools and guidelines already exist, integrating them with enhanced and continuous training of healthcare providers, in parallel with appropriate workplace accommodation measures to reduce chemical exposures (such as fragrance-free practices and the selection of least-toxic products in terms of VOC emissions), is essential to ensure adequate and equitable access to public, occupational, and healthcare settings.

Supplementary Materials

The following supporting information can be downloaded at the website of this paper posted on Preprints.org, Table S1: Survey questions.

Author Contributions

Conceptualization, R.P.; methodology, R.P., J.M., and R.B.; validation, R.P., J.M., and R.B.; formal analysis, N.A.D.; investigation, R.P., J.M., and R.B.; data curation, N.A.D.; writing—original draft preparation, N.A.D.; writing—review and editing, R.P., J.M., R.B., and A.T.; visualization, N.A.D.; supervision, R.P.; project administration, R.P.; funding acquisition, R.P. All authors have read and agreed to the published version of the manuscript.

Funding

Funding for this study was provided by the Association pour la santé environnementale du Québec—Environmental Health Association of Quebec (ASEQ-EHAQ).

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki, and approved by the Institutional Review Board (or Ethics Committee) of Women’s College Hospital Research Ethics Board (Protocol #2020-0157-E).

Data Availability Statement

The data sets generated and analyzed during this study are available from the corresponding author upon reasonable request.

Acknowledgments

The authors thank all the participants experiencing multiple chemical sensitivity (MCS) who took the time and the effort to contribute to the study.

Conflicts of Interest

Some authors received remuneration from (ASEQ-EHAQ) for conducting data analysis and manuscript preparation. However, this did not influence the study design, analysis, or interpretation of results.

Appendix A. Survey Questions

Item Responses possible
General Information – Screening Questions
Q1. What is your age? Less than 18 [end of survey if selected]
13 categories of 10-year intervals from age 18 to age 79
80+
Q2. Country of residence Canada
Other [end of survey if selected]
Q3. When did you start experiencing symptoms of multiple chemical sensitivity MCS? Before March 11, 2019
Between March 11, 2019 and present [end of survey if selected]
Not applicable, I do not suffer from MCS [end of survey if selected]
Demographics
Q4. What is your sex? Female
Male
Other
Prefer not to answer
Q5. What is the highest level of education that you have completed? Less than secondary school
Secondary school graduation
Post-secondary education
Undergraduate degree
Post-graduate certificate
Master’s degree
Doctorate or Postdoctoral degree
Prefer not to answer
MCS Onset and Triggers
Q6. Do you know where your chemical sensitivity/MCS was initiated/started? (Select all that apply) Home
Workplace
Other
Unsure
Q7. Which of the following household exposures do you think initiated your condition? (Select all that apply) Construction or renovation materials
Cooking odors
Cleaning products
Engine exhaust
Disinfectants
Foods
Furnishings
Laundry products
Mould
Scents
Air fresheners
Pesticides
Woodstove emissions
Unknown source
Other
Q8. Which of the following workplace exposures do you think initiated your condition? (Select all that apply) Chemicals from laboratory
Construction or renovation materials
Cooking odors
Diesel or vehicle exhaust
Disinfectants or soaps
Foods
Furniture or carpeting
Industrial cleaning products
Lacquer/varnish
Mould spores/water-damaged building
Paint
Scented air fresheners
Pesticides or insecticides
Photocopier emissions
Printing ink
Scents
Solvents
Textiles or fabrics
Tobacco smoke
Unknown source
Other
Q9. Was your MCS health condition initiated by A single large exposure event
Ongoing exposure/s over a period of time
A series of significant exposures
Unsure
Other
Q10. Do you experience symptoms when inhaling the following despite wearing a mask? Each with: Yes/No/Not applicable
Unscented
disinfectant/Sanitizer
Scented
disinfectant/sanitizer
Unscented soap
Scented soap
Q11. Please indicate your symptom(s) upon exposure, if any, to the following when inhaled: Dropdown list includes (for each of the above triggers)
Brain fog or concentration difficulties
Memory difficulties
Fatigue
Dizziness
Coordination or balance difficulties
Headaches
Irritability
Ear problems
Eye problems
Breathing difficulties
Coughing
Joint and muscle pain
Muscle weakness
Itching
Other skin problems
Cardiovascular problems
Gastrointestinal problems
Urinary problems
Other symptoms
Housing Conditions
Q12. Do you live in safe housing suitable for your MCS health condition?(Safe housing is as follows and should be free of the following: mould, materials that trigger your symptoms (such as paint, new construction/renovation materials), exposures to triggers from neighbours or nearby emissions from traffic or industry, etc. Yes
No
Q13. What is your current housing situation? (Select all that apply) Affordable/social housing
homeless
owner
moving frequently
renting
shelter
tent
vehicle
with family/friends
other
Exposure to Odours & Symptoms
Q14. Were you/are you exposed to the following odours from external sources? Each with: Yes/No/Not applicable
Cleaning products
Cooking odours
Disinfectants/sanitizers
Scents
Home renovation
Incense
Laundry products
Second/third-hand tobacco smoke
Second/third-hand marijuana
Q15. Please indicate symptoms experienced upon exposure to these odours: Dropdown list includes (for each of the above odours):
Brain fog
Memory issues
Fatigue
Dizziness
Breathing difficulties
Coughing
Headaches
Skin problems
Cardiovascular issues
Gastrointestinal problems
Other
Indirect Exposure Through Others
Q16. If you are dependent on others for shopping and they use scented products, do you experience symptoms from the scents on the person or items? Yes
No
Not applicable
Q17. Rate the severity of your symptoms on exposure to these scents Severe
Moderate
Mild
Q18. What do you do with the items that have scents transferred to them during handling? Clean them vigorously
Remove the packaging
Put them outside to off-gas the odour of the scent
Dispose of them in the garbage
Not applicable

References

  1. Miller, C.S.; Palmer, R.F.; Kattari, D.; et al. What initiates chemical intolerance? Findings from a large population-based survey of U.S. adults. Environ. Sci. Eur. 2023, 35, 65. [CrossRef]
  2. American Medical Association. AMA House of Delegates Handbook: 2025 Annual Meeting. Available online: https://www.ama-assn.org/system/files/a25-handbook-combined.pdf.
  3. Zucco, G.; Doty, R. Multiple Chemical Sensitivity. Brain Sci. 2022, 12, 46. [CrossRef]
  4. Del Casale, A.; Ferracuti, S.; Mosca, A.; Pomes, L.M.; Fiaschè, F.; Bonanni, L.; Borro, M.; Gentile, G.; Martelletti, P.; Simmaco, M. Multiple Chemical Sensitivity Syndrome: A Principal Component Analysis of Symptoms. Int. J. Environ. Res. Public Health 2020, 17, 6551. [CrossRef]
  5. Rossi, S.; Pitidis, A. Multiple Chemical Sensitivity: Review of the State of the Art in Epidemiology, Diagnosis, and Future Perspectives. J. Occup. Environ. Med. 2018, 60, 138–146. [CrossRef]
  6. Molot, J.; Sears, M.; Anisman, H. Multiple Chemical Sensitivity: It's Time to Catch Up to the Science. Neurosci. Biobehav. Rev. 2023, 151, 105227. [CrossRef]
  7. Miller, C.S. Toxicant-Induced Loss of Tolerance—An Emerging Theory of Disease? Environ. Health Perspect. 1997, 105 (Suppl. 2), 445–453. [CrossRef]
  8. Steinemann, A. Fragranced Consumer Products: Exposures and Effects from Emissions. Air Qual. Atmos. Health 2016, 9, 861–866. [CrossRef]
  9. Steinemann, A. National Prevalence and Effects of Multiple Chemical Sensitivities. J. Occup. Environ. Med. 2018, 60, e152–e156. [CrossRef]
  10. Bray, R.; Wang, Y.; Argiropoulos, N.; Robins, S.; Molot, J.; Pigeon, M.-A.; Gaudet, M.; Auger, P.; Bélanger, É.; Peris, R. The Impact of COVID-19 Health Measures on Adults with Multiple Chemical Sensitivity: Cross-Sectional Study. JMIR Form. Res. 2024, 8, e48434. [CrossRef]
  11. Robins, S.; Molot, J.; Peris, R. Prevalence of Multiple Chemical Sensitivity in Canada Between 2000 and 2020. Int. J. Environ. Res. Public Health 2026, 23, 236. [CrossRef]
  12. Statistics Canada. Canadian Community Health Survey—Annual Component (CCHS), Survey No. 3226; Government of Canada: Ottawa, ON, Canada, 2025. Available online: https://www23.statcan.gc.ca/imdb/p2SV.pl?Function=getSurvey&SDDS=3226.
  13. Lavric, C.E.; Migueres, N.; de Blay, F. Multiple Chemical Sensitivity: A Review of Its Pathophysiology. Explor. Asthma Allergy 2024, 2, 350–362. [CrossRef]
  14. Masri, S.; Miller, C.S.; Palmer, R.F.; et al. Toxicant-Induced Loss of Tolerance for Chemicals, Foods, and Drugs: Assessing Patterns of Exposure Behind a Global Phenomenon. Environ. Sci. Eur. 2021, 33, 65. [CrossRef]
  15. Alberta Health. Multiple Chemical Sensitivity: Literature Review and State of the Science; Government of Alberta: Edmonton, AB, Canada, 2021. Available online: https://open.alberta.ca/publications/multiple-chemical-sensitivity-literature-review-state-of-science.
  16. Yousufzai, S.J.; Psaradellis, E.; Peris, R.; Barakat, C. A Qualitative Exploration of Policy, Institutional, and Social Misconceptions Faced by Individuals with Multiple Chemical Sensitivity. Int. J. Environ. Res. Public Health 2025, 22, 1383. [CrossRef]
  17. Molot, J.; Sears, M.; Marshall, L.M.; Bray, R.I. Neurological Susceptibility to Environmental Exposures: Pathophysiological Mechanisms in Neurodegeneration and Multiple Chemical Sensitivity. Rev. Environ. Health 2022, 37, 509–530. [CrossRef]
  18. Suzuki, T.; Bai, Y.; Ohno, Y. Prevalence and Factors Related to High Risk of Multiple Chemical Sensitivity Among Japanese High School Students. Int. J. Environ. Res. Public Health 2024, 21, 934.
  19. Caress, S.M.; Steinemann, A.C. A Review of a Two-Phase Population Study of Multiple Chemical Sensitivities. Environ. Health Perspect. 2003, 111, 1490–1497.
  20. Hojo, S.; Ishikawa, S.; Kumano, H.; Miyata, M.; Sakabe, K. Clinical Characteristics of Physician-Diagnosed Patients with Multiple Chemical Sensitivity in Japan. Int. J. Hyg. Environ. Health 2008, 211, 682–689. [CrossRef]
  21. Claeson, A.S.; Andersson, L. Symptoms from Masked Acrolein Exposure Suggest Altered Trigeminal Reactivity in Chemical Intolerance. Neurotoxicology 2017, 60, 92–98. [CrossRef]
  22. Talavera, K.; Startek, J.B.; Alvarez-Collazo, J.; Boonen, B.; Alpizar, Y.A.; Sanchez, A.; et al. Mammalian Transient Receptor Potential TRPA1 Channels: From Structure to Disease. Physiol. Rev. 2020, 100, 725–803.
  23. Stevens, J.F.; Maier, C.S. Acrolein: Sources, Metabolism, and Biomolecular Interactions Relevant to Human Health and Disease. Mol. Nutr. Food Res. 2008, 52, 7–25.
  24. Weschler, C.J. Ozone's Impact on Public Health: Contributions from Indoor Exposures to Ozone and Products of Ozone-Initiated Chemistry. Environ. Health Perspect. 2006, 114, 1489–1496.
  25. Agency for Toxic Substances and Disease Registry (ATSDR). Toxicological Profile for Acrolein; U.S. Department of Health and Human Services: Atlanta, GA, USA, 2025. Available online: https://www.atsdr.cdc.gov/toxprofiles/tp124.pdf.
  26. Berenguer, P.; Soulage, C.; Perrin, D.; Pequignot, J.M.; Abraini, J.H. Behavioral and Neurochemical Effects Induced by Subchronic Exposure to 40 ppm Toluene in Rats. Pharmacol. Biochem. Behav. 2003, 74, 997–1003. [CrossRef]
  27. Sorg, B.A.; Tschirgi, M.L.; Swindell, S.; Chen, L.; Fang, J. Repeated Formaldehyde Effects in an Animal Model for Multiple Chemical Sensitivity. Ann. N. Y. Acad. Sci. 2001, 933, 57–67. [CrossRef]
  28. Bowen, S.E.; Balster, R.L. Tolerance and Sensitization to Inhaled 1,1,1-Trichloroethane in Mice: Results from Open-Field Behavior and a Functional Observational Battery. Psychopharmacology 2006, 185, 405–415. [CrossRef]
  29. Ho, C.Y.; Lee, L.Y. Ozone Enhances Excitabilities of Pulmonary C Fibers to Chemical and Mechanical Stimuli in Anesthetized Rats. J. Appl. Physiol. 1998, 85, 1509–1515.
  30. Alpizar, Y.A.; Boonen, B.; Gees, M.; Sanchez, A.; Nilius, B.; Voets, T.; Talavera, K. Allyl Isothiocyanate Sensitizes TRPV1 to Heat Stimulation. Pflugers Arch. 2014, 466, 507–515.
  31. Mo, X.; Liu, Q.; Gao, L.; Xie, C.; Wei, X.; Pang, P.; Tian, Q.; Gao, Y.; Zhang, Y.; Wang, Y.; Xiong, T.; Zhong, B.; Li, D.; Yao, J. The Industrial Solvent 1,4-Dioxane Causes Hyperalgesia by Targeting Capsaicin Receptor TRPV1. BMC Biol. 2022, 20, 10.
  32. Bhave, G.; Zhu, W.; Wang, H.; Brasier, D.J.; Oxford, G.S.; Gereau, R.W. IV. Protein Kinase C Phosphorylation Sensitizes but Does Not Activate the Capsaicin Receptor TRPV1. J. Neurosci. 2002, 22, 3027–3035.
  33. Mohapatra, D.P.; Nau, C. Desensitization of Capsaicin-Activated Currents in the Vanilloid Receptor TRPV1 Is Decreased by PKC-Mediated Phosphorylation. J. Biol. Chem. 2003, 278, 5008–5016.
  34. Bautista, D.M.; Jordt, S.E.; Nikai, T.; Tsuruda, P.R.; Read, A.J.; Poblete, J.; Yamoah, E.N.; Basbaum, A.I.; Julius, D. TRPA1 Mediates the Inflammatory Actions of Environmental Irritants and Proalgesic Agents. Cell 2006, 124, 1269–1282. [CrossRef]
  35. Hinman, A.; Chuang, H.H.; Bautista, D.M.; Julius, D. TRP Channel Activation by Reversible Covalent Modification. Proc. Natl. Acad. Sci. USA 2006, 103, 19564–19568. [CrossRef]
  36. Woolf, C.J. Central Sensitization: Implications for the Diagnosis and Treatment of Pain. Pain 2011, 152 (Suppl. 3), S2–S15.
  37. Gibson, P.R.; Vogel, V.M. Sickness-Related Dysfunction in Persons with Self-Reported Multiple Chemical Sensitivity at Four Levels of Severity. J. Clin. Nurs. 2009, 18, 72–81. [CrossRef]
  38. Lacour, M.; Zunder, T.; Schmidtke, K.; Vaith, P.; Scheidt, C. Multiple Chemical Sensitivity Syndrome (MCS)—Suggestions for an Extension of the U.S. MCS Case Definition. Int. J. Hyg. Environ. Health 2005, 208, 141–151. [CrossRef]
  39. Cullen, M.R. The Worker with Multiple Chemical Sensitivities: An Overview. Occup. Med. 1987, 2, 655–661.
  40. Multiple Chemical Sensitivity: A 1999 Consensus. Arch. Environ. Health 1999, 54, 147–149. [CrossRef]
  41. Saito, M.; Kumano, H.; Yoshiuchi, K.; Kokubo, N.; Ohashi, K.; Yamamoto, Y.; Shinohara, N.; Yanagisawa, Y.; Sakabe, K.; Miyata, M.; Ishikawa, S.; Kuboki, T. Symptom Profile of Multiple Chemical Sensitivity in Actual Life. Psychosom. Med. 2005, 67, 318–325. [CrossRef]
  42. Fares-Medina, S.; Díaz-Caro, I.; García-Montes, R.; Corral-Liria, I.; García-Gómez-Heras, S. Multiple Chemical Sensitivity Syndrome: First Symptoms and Evolution of the Clinical Picture. Int. J. Environ. Res. Public Health 2022, 19, 15891. [CrossRef]
  43. Hausteiner, C.; Bornschein, S.; Hansen, J.; Zilker, T.; Förstl, H. Self-Reported Chemical Sensitivity in Germany: A Population-Based Survey. Int. J. Hyg. Environ. Health 2005, 208, 271–278. [CrossRef]
  44. Guerrero, A.; Ramírez, L.; Orpella, X.; et al. Multiple Chemical Sensitivity Syndrome: Analysis of Cases Visited in Our Occupational Health Unit from 2011 to 2015. Occup. Environ. Med. 2016, 73, A218.
Table 1. Sociodemographic characteristics.
Table 1. Sociodemographic characteristics.
Sample Characteristics n (N=119) %
Sex
Male 16 13%
Female 103 87%
Age group (years)
25-34 9 8%
35-44 23 19%
45-54 19 16%
55-64 43 36%
65-74 19 16%
75 and over 6 5%
Education
Secondary school 9 7%
College 40 34%
University 68 57%
Prefer not to answer 2 2%
Table 2. Location of MCS onset.
Table 2. Location of MCS onset.
Location n (N=119) %
Workplace 66 55
Home 42 35
Other 30 25
Unsure 4 3
*Totals may exceed 100% because participants could select multiple responses.
Table 3. Exposure events associated with onset of MCS.
Table 3. Exposure events associated with onset of MCS.
Event n (N= 119) %
Ongoing exposure/s over a period of time 72 61
A series of significant exposures 36 30
Other** 24 20
Unsure 21 18
A single large exposure 20 17
*Totals may exceed 100% because participants could select multiple responses. ** ‘Other’ responses include: ‘mould, bleach, urea-formaldehyde over a period of months’, ‘two (exposure) events’ and ‘35 years working as a hairdresser’.
Table 4. Workplace exposures associated with onset of MCS.
Table 4. Workplace exposures associated with onset of MCS.
Trigger n (N= 66) %
Scented air fresheners 30 45%
Scents 29 44%
Industrial cleaning products 24 36%
Construction or renovation materials 22 33%
Disinfectants or soaps 20 30%
Mould spores/water-damaged building 20 30%
Paint 17 26%
Furniture or carpeting 16 24%
Pesticides or insecticides 15 23%
Photocopier emissions 15 23%
Diesel or vehicle exhaust 14 21%
Printing ink 14 21%
Solvents 11 17%
Chemicals from laboratory 10 15%
Lacquer/varnish 10 15%
Other** 9 14%
Unknown source 8 12%
Tobacco smoke 6 9%
Foods 3 5%
Cooking odours 2 3%
Textiles or fabrics 2 3%
* Totals may exceed 100% because participants could select multiple responses. ** ‘Other’ responses included ‘Tobacco, marijuana, smoked street drugs, incense’, ‘Art supplies’, ‘H1N1 influenza’, and ‘house renovations, i.e., paints, cleaners, solvents’.
Table 6. Self-reported symptoms despite mask use.
Table 6. Self-reported symptoms despite mask use.
Trigger n (N = 119) %
Unscented disinfectant/sanitizer
Yes 64 54%
No 55 46%
Scented disinfectant/sanitizer
Yes 112 94%
No 7 6%
Unscented soap
Yes 23 19%
No 96 81%
Scented soap
Yes 107 90%
No 12 10%
Table 7. Symptoms by trigger type (N=119).
Table 7. Symptoms by trigger type (N=119).
Symptoms Scented disinfectant/sanitizer
n (%)
Unscented disinfectant/sanitizer
n (%)
Scented soap
n (%)
Unscented soap
n (%)
Brain fog or concentration difficulties 78 (66%) 37 (31%) 75 (63%) 10 (8%)
Memory difficulties 64 (54%) 29 (24%) 58 (49%) 10 (8%)
Fatigue 73 (61%) 36 (30%) 65 (55%) 13 (11%)
Dizziness 66 (56%) 25 (21%) 58 (49%) 7 (6%)
Coordination or balance difficulties 52 (44%) 22 (18%) 48 (40%) 5 (4%)
Headaches 84 (71%) 44 (37%) 78 (66%) 14 (12%)
Irritability 72 (61%) 29 (24%) 70 (59%) 11 (9%)
Ear problems 30 (25%) 16 (13%) 28 (24%) 6 (5%)
Eye problems 44 (37%) 23 (19%) 43 (36%) 7 (6%)
Breathing difficulties 75 (63%) 42 (35%) 72 (61%) 13 (11%)
Coughing 65 (55%) 38 (32%) 59 (50%) 11 (9%)
Joint and muscle pain 43 (36%) 22 (19%) 42 (35%) 12 (10%)
Muscle weakness 40 (34%) 17 (14%) 40 (34%) 9 (8%)
Itching 47 (40%) 24 (20%) 48 (40%) 14 (12%)
Other skin problems 34 (29%) 20 (17%) 34 (29%) 11 (9%)
Cardiovascular problems 28 (24%) 13 (11%) 26 (22%) 5 (4%)
Gastrointestinal problems 39 (34%) 15 (13%) 37 (31%) 8 (7%)
Urinary problems 20 (17%) 9 (8%) 20 (17%) 5 (4%)
Other symptoms† 22 (19%) 13 (11%) 23 (19%) 10 (8%)
* Totals may exceed 100% because participants could select multiple responses. ** ‘Other’ responses included ‘Burning and pain in lungs’, ‘Voice changes’, ‘Burning and irritation in the sinus’, ‘Lip swelling, face and throat swelling’, ‘Difficulty walking’, ‘Rashes, eczema’, ‘Nausea’.
Table 8. Triggers entering the home environment.
Table 8. Triggers entering the home environment.
Trigger n (N=119) %
Laundry products 85 71%
Scents 76 64%
Disinfectants/sanitizers 70 59%
Cleaning products 67 56%
Cooking odours 65 55%
Second/third-hand tobacco smoke 45 38%
Second/third-hand marijuana 37 31%
Home renovation 31 26%
Incense 21 18%
*Totals may exceed 100% because participants could select multiple responses.
Table 10. Symptoms triggered by specific exposures (N=119).
Table 10. Symptoms triggered by specific exposures (N=119).
Symptom Cleaning products Disinfectants/sanitizers Scents (perfume, cologne) Laundry products
Brain fog 82 (69%) 74 (62%) 79 (66%) 70 (59%)
Headaches 81 (68%) 76 (64%) 81 (68%) 67 (56%)
Fatigue 81 (68%) 71 (60%) 75 (63%) 70 (59%)
Breathing difficulties 73 (61%) 71 (60%) 76 (64%) 73 (61%)
Irritability 71 (60%) 67 (56%) 73 (61%) 60 (50%)
Memory difficulties 67 (56%) 63 (53%) 65 (55%) 54 (45%)
Dizziness 61 (51%) 55 (46%) 64 (54%) 54 (45%)
Coughing 63 (53%) 58 (49%) 67 (56%) 55 (46%)
Coordination or balance problems 48 (40%) 49 (41%) 52 (44%) 42 (35%)
Eye problems 44 (37%) 45 (38%) 48 (40%) 40 (34%)
Joint and muscle pain 55 (46%) 48 (40%) 48 (40%) 42 (35%)
Gastrointestinal problems 48 (40%) 38 (32%) 44 (37%) 42 (35%)
Muscle weakness 42 (35%) 35 (29%) 43 (36%) 39 (33%)
Itching 48 (40%) 37 (31%) 39 (33%) 37 (31%)
Ear problems 31 (26%) 29 (24%) 31 (26%) 23 (19%)
Other skin problems 35 (29%) 32 (27%) 29 (24%) 31 (26%)
Cardiovascular problems 30 (25%) 27 (23%) 32 (27%) 25 (21%)
Urinary problems 23 (19%) 15 (13%) 18 (15%) 18 (15%)
Other symptoms† 29 (24%) 24 (20%) 23 (19%) 24 (20%)
* Totals exceed 100% because participants could select multiple symptoms for each source. ** ‘Other’ responses included ‘Muscle spasms, arthritis, sore throat, difficulty swallowing’, ‘Face feels swollen, changes in body odour’, ‘Burning and pain in lungs, pain in trunk of body, in head and in liver’.
Table 11. Housing characteristics of participants.
Table 11. Housing characteristics of participants.
Housing characteristic n (N=119) %
Access to safe housing suitable for MCS
Yes 57 48
No 62 52
Current housing situation
Affordable/social housing 6 5
Unstable housing (homeless, moving frequently, shelter, tent, vehicle, with family/friends, etc.) 18 15
Owner 51 43
Renting 42 35
Other 2 2
*Percentages may not total 100 due to rounding.
Table 12. Indirect exposures (third-hand) and severity of symptoms.
Table 12. Indirect exposures (third-hand) and severity of symptoms.
Variable n (N=110) %
Symptoms from scents on people/items during assisted shopping* n (N=110) %
Yes 81 74
Not applicable 29 26
Severity of symptoms reported on indirect exposure to these scents %
Severe 43 53
Moderate 34 42
Mild 4 5
Did not answer 29 36
Actions taken for items with scent transfer during handling n (N=90) %
Put them outside to off-gas the odour of the scent 55 61
Dispose of them in the garbage 41 46
Clean them vigorously 49 54
Remove the packaging 61 68
*Assisted shopping refers to situations in which participants relied on another person to shop for their essential needs. ** Totals may exceed 100% because participants could select multiple responses.
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