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Meet The Team: England - UK

Andy Croft: Country Coordinator

Andy Croft, MCS International Country Coordinator for England, UK. The Chemical Connection:  I was diagnosed with M.E. and hypothyroidism several months after moving into a newly renovated home in 2005, I was largely unaware of any chemical connection at that time. My discovery only came about when my symptoms got much better whilst staying with family. On returning to my house the symptoms soon got worse again. These included aching muscles and joints, headaches, nausea, eye/nose/throat irritation, swollen lymph glands, insomnia, unexplained allergic skin reactions, fatigue and the inevitable depression as work became untenable and life ground to a halt. Anyone unfortunate enough to relate to these kind of symptoms from experience will know how debilitating they can be, especially since they tend to be present all at once. I count myself very lucky not to be suffering as acutely as some and lucky also to have managed to hang onto my home and sanity!

At the time of the house move I was in pretty good health although I was already intolerant to alcohol and various pharmaceutical medications as well as milk and wheat. I also began instinctively avoiding the use of perfumed and chemical-laden aftershaves, deodorants, toiletries and household cleaning fluids many years ago; they all seemed palpably noxious as well as irritating my skin. These signs all add up to a classic picture of someone with a weakened immune system and are common amongst those diagnosed with M.E. They also all point to the fact that a chemical connection (if not the foundation in at least some cases) to M.E. is quite obvious. Certainly the more I learn about my condition and the more people I have met with M.E., the more compelling that idea has become.

Background Information:  I'm 38 years old and living in Norfolk, England. I was running my own business as a graphic designer but my health problems have meant that my career has been sidelined for the time being. One of the greatest problems I have had to face (aside from having to curtail most social aspects of my life in order to avoid inevitable poisoning and resultant illness) is a lack of understanding and even disbelief amongst family, friends and work colleagues - it's isolating and frustrating. Communications with Gordon McHendry and others at MCS-International and working with my local M.E. Support Group have been an enormous help in this regard.

I've managed to detoxify my previously 'sick' house (as much as possible, still something of a work in progress!!) by removal of synthetic carpets, MDF, and painting walls with special paints (which were particularly troublesome since they had all been recently replastered). I'm now able to live in the property but continue to be dogged by M.E. symptoms and a high degree of chemical sensitivity that I had not experienced before renovating the house, most noticeably to perfumes/after shaves which trigger instant headaches and to traffic fumes. I wear a carbon filter mask when I venture out in the car on longer journeys or in heavy traffic and, yes, I get some pretty curious looks from other drivers!

The Wider Context:  Before my discovery of MCS, I was already a convert to the benefits of nutritional therapy, which helped me to conquer depression and unexplained fatigue in the past when I found I was intolerant to pharmaceutical treatments. I have a great interest in this area (now becoming known as ecological or functional medicine) and see diet, nutrition and toxic avoidance as the logical panacea for treatment, not just of MCS but of a great many common diseases and illnesses. Furthermore I believe the current Western pharmaceutical approach to medicine is almost as harmful and dangerous as the global proliferation of toxic chemicals. They're a terrifying prospect in combination and if we don't make some fundamental changes we genuinely risk becoming an endangered species within a few generations.

Although official medical recognition of MCS is of the greatest importance, I believe that success in changing the climate of public opinion regarding toxic chemicals will rely on amassing the support of sufferers of all forms of chemical (and EM radiation) related illness and those concerned with their care. The scope of chemical related illness does not stop with MCS, ME and CFIDS but encompasses a vast assortment of recognised medical complaints, syndromes and diseases that have become commonplace in Western industrialised nations where the use and prevalence of synthetic and petro chemicals in our food, our air and our water is now ubiquitous. There is surely enough evidence to support the fact that the burden of toxic chemicals is linked to the rising incidence of asthma which now affects an alarming proportion of children worldwide. Asthma is the very tip of the chemical related illness iceberg: chemical toxicity has also been linked to aspergers syndrome, autism, ADHD, bipolar disorder, birth defects, cancer, clinical depression, criminal delinquency... that's just a few things beginning with a,b and c that I can think of. The list is potentially massive. With this in mind, I believe that there is already a critical mass of sufferers of chemical related illness of one sort or another who can facilitate real change if united in their cause. The first step in this is communicating a critical awareness of the toxic chemical connection to all groups and communities concerned with the care and rights of the chemically injured.

I'm pleased to offer my services as the MCS International rep for England and join a team of people who care enough to want to try and make a positive change to public perception and policy making in order to lead us into a less toxic future. It's an enormous task but I believe that truth will prevail. My only hope is that we don't have to reach pandemic proportions of illness and suffering before the tide is ready to turn.

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