Written by our acting Trustee, Sarah Scotts Open Access write up on Electrosmog and EMF exposure highlights everyday exposures, current research and health concerns, as well as steps governments and individuals can take to support protection. It was first published on the Open Access Government website and later featured in their October digital...
Note that this is summary that we've gathered from being part of an MCS taskforce - (not intended as clinical guidance). Early Immune System Research in Multiple Chemical Sensitivity (MCS) What past studies found — and what it may mean today In the 1980s and 1990s, several research groups investigated whether the immune...
The 'La Presse' has published a response from The Environmental Health Association of Canada, defending fragrance-free environments and the rights of people living with Multiple Chemical Sensitivity. This is great news and a significant breakthrough for our MCS community. 'Le Presse' a French- language digital news outlet, with content available...
MCS Aware welcomes the release of the initial findings from the DecodeME DNA study, the largest genetic study in the world focused on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). These landmark results offer powerful, science-backed evidence that ME/CFS is not just “all in the mind”, but has a biological and genetic...
Recent developments in government welfare reforms have caused confusion and concern, particularly for people living with long-term health conditions like Multiple Chemical Sensitivity (MCS), ME/CFS, and related disorders. Many of our members rely on Personal Independence Payment (PIP) and Universal Credit (UC), so here’s what you need to know. PIP 4-Point...
Hello Let me introduce myself. I am MaLou, I live in Warwickshire and I have been living with Chemical Sensitivities for over thirty years. Whilst it is a heavy burden on my life it has gifted me an awareness of the impact that chemicals have in our garden. The natural ecosystem...
My name is Cathy and I am 63, single and have lived alone since the death of my mother in 2020. I was a carer for my mother in her final nine years when she developed Alzheimer's. I live in Sheffield in the UK. I have been unwell since childhood but...
We are taking the opportunity this May for international MCS Awareness month, to raise awareness of this misunderstood illness and promote how to raise funds for MCS Aware. Below you can read a heartfelt poem from one of our longstanding members who has been severely impacted by the symptoms of Multiple...
Through the Looking Glass As I gaze into the looking glass-what do I see? A WHOLE WORLD on the other side beckoning me! Family meals, warm log fires, a fun-filled holiday All the things that freedom brings, a mere hairs breadth away. As I reach out my hand, I touch cold glass And I wonder what...
Name: Marie Age: 44 Gender: Female Relationship status: Single Family Situation: no children Employment: Unemployed since August 2024 (due to illness including MCS) Residential Status: Living with family Geographical residence; Belfast I have been living with difficulties around exposure to some chemicals and fragrances for approximately 18 years. This became worse in work since July 2023 when...
