Guest guest Posted July 23, 2011 Report Share Posted July 23, 2011 Hello, I am sorry, but I do not see any advantage by such an initiative. There are already thousands of such personal stories, but they do not presnt any solutions. The symptoms are the same, but every person reacts differently. I do know ALL the symptoms of electrosensitivity. So what? If you do not look at the problemacy with an *open mind*, you will never find a solution. I have written a piece how a serious test for electrosensitivity should be done. And how electrosensitivitry should be looked at. And why all those studies so far are rubbish. Real trash. Most scientists do not have the faintest idea what it is all about. It is in dutch. When I have time, I will translate it, and place it here. Greetings, Claessens member Verband Baubiologie www.milieuziektes.nl www.milieuziektes.be www.hetbitje.nl checked by Norton Stories from ES-ers for book >From mast-victims.org: I would like to invite your help for a book I'm currently writing on electromagnetic hypersensitivity. I am looking for people who will share their stories about how they are affected by EMR and how they are dealing with this. I am particularly interested in stories of people who have recovered from the condition and the methods they have used. I would be grateful if you could let any of your members know about this opportunity to share their story in print. Here's the message I have put on my facebook page: Do you experience any discomfort when you use a mobile or cordless phone, when you use a computer or when you spend time near other equipment that emits electromagnetic signals? If you do, would you be willing to share your story with me? My new book is about these sorts of symptoms and what people can do about them. I'd love to hear your story, too. Many thanks indeed Lyn McLean (Author 'The Force - living safely in a world of electromagnetic pollution', 2011, and 'Watt's the Buzz? Understanding and avoiding the risks of electromagnetic radiation', 2002.) LM76543@... Source: http://www.mast-victims.org/index.php?content=news & action=view & type=newsitem & id=\ 5314 ------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2011 Report Share Posted July 23, 2011 ,  I think it's good to spread awareness of this insidious impairment. I also think that methods used by others to reduce sensitivities may not work for all because we are all different; agreed! However, it may give some help to those who try what is suggested. So it is for those two reasons I think another book is great!  Well there is another. I think that other's stories may give comfort to those who have been ostricized socially by the stigma of EHS.  Loni  From: charles <charles@...> Subject: Re: Stories from ES-ers for book Date: Saturday, July 23, 2011, 5:33 AM  Hello, I am sorry, but I do not see any advantage by such an initiative. There are already thousands of such personal stories, but they do not presnt any solutions. The symptoms are the same, but every person reacts differently. I do know ALL the symptoms of electrosensitivity. So what? If you do not look at the problemacy with an *open mind*, you will never find a solution. I have written a piece how a serious test for electrosensitivity should be done. And how electrosensitivitry should be looked at. And why all those studies so far are rubbish. Real trash. Most scientists do not have the faintest idea what it is all about. It is in dutch. When I have time, I will translate it, and place it here. Greetings, Claessens member Verband Baubiologie www.milieuziektes.nl www.milieuziektes.be www.hetbitje.nl checked by Norton Stories from ES-ers for book >From mast-victims.org: I would like to invite your help for a book I'm currently writing on electromagnetic hypersensitivity. I am looking for people who will share their stories about how they are affected by EMR and how they are dealing with this. I am particularly interested in stories of people who have recovered from the condition and the methods they have used. I would be grateful if you could let any of your members know about this opportunity to share their story in print. Here's the message I have put on my facebook page: Do you experience any discomfort when you use a mobile or cordless phone, when you use a computer or when you spend time near other equipment that emits electromagnetic signals? If you do, would you be willing to share your story with me? My new book is about these sorts of symptoms and what people can do about them. I'd love to hear your story, too. Many thanks indeed Lyn McLean (Author 'The Force - living safely in a world of electromagnetic pollution', 2011, and 'Watt's the Buzz? Understanding and avoiding the risks of electromagnetic radiation', 2002.) LM76543@... Source: http://www.mast-victims.org/index.php?content=news & action=view & type=newsitem & id=\ 5314 ------------------------------------ Quote Link to comment Share on other sites More sharing options...
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