• 

  Verasak said,

  Thank Lloyd for dedicating his time on this.

• 

  Walter Vohradsky said,

  Thanks LLoyd, loking forwar to the followup video(s).

• 

  Dave said,

  wanted to make sure you had seen two articles on ES I had recently seen–

  one about Brian Clement

  http://marylandsmartmeterawareness.org/general-info/health-concerns/electrosensitivity-symptoms-can-be-eliminated-in-60-of-people-and-significantly-reduced-in-the-rest-dr-brian-clement/

  and one about Prof Belpomme in France

  http://mieuxprevenir.blogspot.com/2012/06/electrosensitivity-es-ehs.html

  A NIS practitioner, a practice that has some reported success with ES, may also be of interest

  http://www.neurolinkglobal.com/Electro_270.aspx

  I have contacted a NIS practitioner in my area, but have yet to have a session with him

  the suggested relationship between heavy metals and ES makes sense in my experience. There is a product called “Metal Magic” available through “Baseline Nutritionals” that may be VERY helpful

  in four years of daily searching for answers on this subject, these are some of the most helpful things I have found–along with your site–

  wishing you well

  Dave Schock

• 

  Lloyd said,

  Hi Dave
  I had not heard of the NIS practitioner but I am familiar with the work of Professor Belpomme and Brian Clement.
  I met Professor Belpomme a few years back, I have written a few articles about his work see http://www.electricsense.com/2672/electrosensitivity-a-physical-illness-that-can-be-diagnosed/
  I am not quite sure what to make of Brian Clement. I read the article you mentioned about a month ago and sent him a message from his Hippocrates website but got no reply. He makes some fairly spectacular claims about curing people from electrical sensitivity which I would like to believe, but the jury is still out for me on this….
  Thanks for sharing.

• 

  Kamele said,

  I very much appreciate all of your efforts, Lloyd, at informing the public on the problem with EMF sensitivity and dangers. One of the hardest things for me to deal with is convincing those who do not suffer from (or are not “feeling” the effects of) EMF that it is REAL and it is painful. I guess that most people will not really believe until it happens to them. I’m sure that everyone has their overload point. I just hate to see folks have to get there just because it’s more convenient to ignore the truth. But keep up the good work. I’m glad we have you to back up those of us who are suffering in this way. Are you familiar with the MEMON devices, and are they really effective? I look forward to Part 2.
  I wish you blessings and continual DE-FUZZING,
  Kamele, Georgia, USA

• 

  Lloyd said,

  Hi Kamele
  I have not tried the particular brand of device you are talking about so it’s unfair to criticize but I have tried all sorts of pendants and neutralizers…many of them are quite expensive and none of them have worked, for me. I believe the solution lies elsewhere…
  As far as convincing the non-believers is concerned, if somebody asks my opinion on this subject then I give it to them if I see a baby or small child using a cell phone then I might say something, but that’s as far as it goes. I gave up a long time ago trying to convince people about the dangers of EMFs and I live better for it. The people that know you, your loved ones, they know about the dangers they can see what it does to you. For the others, unless you see yourself as some sort of EMF crusader, I think you are better leaving it alone and focusing your energies elsewhere.

• 

  Paul Von said,

  Here is a comment from the Brian Clement web site.

  “I do not particularly like jewelry, but I wear a pendant around my neck that acts as an EMF shield. Many of these devices work. I use a Gia computer chip on all our computers and our cell phones.”

  I was with him all the way up to the totally unrealistic, and scientifically invalid statements above.
  I have a thirty-eight year history in electronics design and applications, and it is obvious this man doesn’t know higher math, physics, cellular biology, or how to tell a personal fiction from a scientific fact.

  People like Mr. Clement make a mockery out of science, a practice that makes it all that much easier for governments to pound more nails into the coffins of people like myself.

  Thank you Mr. Clement, you ass.

• 

  Ruth Ruddock said,

  Hi Lloyd,
  Hoping to be able to buy your book soon…would prefer a hard copy over E-book, if possible. I am on a slow dial-up type service right now and can not get the video to play at all (sigh) so would like info to buy the book.
  Also, quick comment on one thing that I know otheres are using (see Planet Thrive website) and that is the Gupta and Annie Hopper Brain Retraining techniques… there are many testimonies from folks on there who have had success ridding themselves of MCS AND EHS, since the two often coexist (as they do with me)and these folks are credible and returning to normal lives again after using these techniques. Please comment on this if you will.
  Right now my EHS symptoms seem to be all centered in one area for me…tinnitus and hearing blockage…I can be a few feet from a person and not hear their words!
  The ringing is so loud and hearing gets blocked incredibly much…otherwise I do not have the symptoms that so many talk about: headaches, pain, etc.

  Ruth/Wisconsin

• 

  Lloyd said,

  Hi Ruth
  For some people ES means tinnitus and hearing problems for others it means headaches and fatigue for others it means something different again. One of the peculiarities of this condition is that no two people have exactly the same symptoms but what everyone who has it does share is a reaction to EMFs.
  Initially my book will be in a downloadable form that you can print out and in audio (mp3) format. But there will be a hard copy version soon to follow. As for the website you mention, I can’t make any specific comments because until you mentioned it I had never heard of them. I did notice what they were selling went with a fairly hefty price tag (several hundred $) my book will not cost anything like this. Not that that makes it better or worse, what matters is what works and for me it has worked.

• 

  rere said,

  Thank Lloyd for this .

• 

  Virginia Houck said,

  Hi,

  When will your book be available for purchase?

• 

  Lloyd said,

  Hi
  I hope to have it out within 7 to 10 days – maximum. It will only be available for purchase through my website initially.

• 

  Virginia Houck said,

  Wonderful! I want 5 copies and look forward to the announcement that we can order. Thank you so much for such a contribution to our health!

• 

  Cassandra said,

  Dear Lloyd,

  Thank you so much for the most helpful information you are sending me since a couple of months. On this last day of the year I would like to wish you all the best for 2013; I do hope that the coming year more and more people will become aware of the poisoning health effects of EMF’s and will take actions.

  I am a Belgian (Flemish) woman of 64 years old and started making the link between my ever increasing health problems and over-exposure to EMF’s about 3-4 years ago. At that time I was still living in the centre of the historic city of Mechelen, after having organised and guided garden tours for 15 years (mainly to the UK, but also to Ireland, France, Italy, Azores,… ) In 2010 I decided to sell my house and went on search for a radiation free zone (!?) in Wallonie (the French speaking part of Belgium). I bought a plot of land in Cens (Tenneville), a tiny village in the Province of Luxemburg, the greenest and less populated region of Belgium. I will soon start with building a new house. In the meantime I am renting the first floor of a barn transformed into two apartments in 2005; I knew from the beginning that it was not what one would call a healthy place to live (electrical heating, poor insulation, a lot of synthetic material, ..) but it was affordable and only 2 km from my new land. In summertime when I can garden most of the day I am quite OK. But living here in wintertime is very hard for me. The last 5 years I spent 3/4 weeks in January/February on La Gomera, one of the least touristic Canary Islands. Unfortunately I saw the number of masts in the mountains increasing every year, the beach restaurants having Free WIFI, … But last year I discovered a tiny hamlet in an idyllic valley well protected from masts and no WIFI around and I could there for 3 weeks after explaining my EHS problem to a German man who lives there. I have the opportunity to go back there from January 17 until February 12. The only problem is getting there without harming my health too much; there is the Ryan Air flight to Tenerife and than the ferry (Wifi !) to La Gomera. I bought already a protective hat and shirt, but my osteopath who tested them on my body (with kinesiology) says they are even weakening me. I know staying at home would be the safest, but I desperately need the sun !

  Do you have any travelling suggestions for people with EHS ?

  Do you know if there exists a list with radiation free accomodation in other countries ?

  Thank you so much for your efforts to help EHS people.

  Best regards and have a nice new year’s eve and day.

  PS : I have a particular reason for choosing Cassandra as a nickname.
  Why I will tell you another time.

• 

  Lloyd said,

  Hi (Cassandra)
  I still like to travel by plane, I recount my story of a recent flight I made and give travel tips in this article http://www.electricsense.com/958/flying-and-electromagnetic-radiation/
  What I didn’t talk about in this article was the accommodation side of things. The main thing I look out for is WiFi. I research on the Internet first, but then I always telephone to the hotel because WiFi may have been installed since the website was last updated. I ask for a room away from lift shafts and electricity power boxes, again this I do by telephone…I explain my ‘problem’ and people are generally very taken aback by my request but they are usually very accommodating. Sometimes they don’t have the answers to my questions in which case it boils down to making a decision. Its usually a family decision to go somewhere so if that place really fits for everyone else but not quite for me, I usually end up by taking a risk and then asking to change on arrival if the room is not suitable.
  Unfortunately I don’t have a list of accommodation suitable for people with ES, but if anyone else knows of such accommodation I will be happy to post it on this website.
  Happy New Year to you!

• 

  Jana said,

  Hallo Lloyd,
  I would like to ask you about static electricity – my partner is having serious pain in the body because of that. As soon as he would touch something what is producing statics his hands turn red. When he grounded himself for first time, he could literally feel how that static electricity is going out. But he has to repeat this grounding. Have you got any experience with this static electricity problem? My partner is saying that he can feel that static electricity in him, no just on the skin.

• 

  Lloyd said,

  Hi Jana
  Static electricity is an electric charge generally caused by friction….some people seem to be more affected by it than others. Things your partner can do; try going barefoot more often (in safe environments-), wearing shoes with leather soles, raising the air humidity in rooms where he spends time – plants can help with this or even just standing a dish of water in the room.

• 

  Kelly Miller said,

  Hi Lloyd
  I started posting earlier and got to a point, I couldn’t function at all. When I tried, everything seemed to be scrambled and confused. I had an electrical stim pain blocker implant taken out, and the following day, with 60 staples in my back and in pain, my thoughts became clearer, sensations, food cravings I thought were lost, returned overnight and continue to. A judge ruled me 100% permanent total disabled. I’d expected an appeal from insurance, after all they’ve put me thru, but it never happened. I’m still regaining my composure, but I think I have to thank you. The meter I have and use stays fairly steady, in safe areas and nothing like before. What I learned on your site may have saved my life.
  Thank You very much Lloyd Burrel!

• 

  Lloyd said,

  Hi Kelly
  Thank you! for your support, and good luck.

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