Coming out

Recently I run into friends who I became kind of close with. They asked me for my cell phone number, and I told them I do not have a cell phone. They asked me if it was due to my choice. I guess they kind of suspected something, so I told them that I became electromagnetic hypersensitive 3 years ago and I no longer have a cell phone. They did not react as much as I thought they would do. They asked me what else I am affected to and I told them fluorescent light. They were kind enough to point to the positive and told me that sometimes being away from cell phone without distraction is a good thing.
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Recovering in Progress

I have been saying that my condition has been improving, but I am still EHS. The other day, I had to go to attorney’s office in downtown about the accident I had. I was rear ended and the other insurance company is not paying much for it, so the attorney wanted to talk to me in person and explain me my options.

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My New Year’s Resolution

In 2017, I hope to cure emf sensitivity or make a major progress. In order to do that, I have to stick to my regimen and go to bed earlier. I have not been very active on the blog, because my condition has been improved and there is not much new. The EMF sensitivity developed kind of all the sudden almost 3 years ago. It just needed a trigger event and all went down hill very quickly. The recovery is not something that can happen all the sudden. It is slow gradual up hill climbing.

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Two and half years since I became EHS

These days, I do not do much research on EMF hypersensitivity. As some point, I stopped discovering new things because I searched so much, so I just continue with my regimen and hope to be cured eventually. A lot have happened in 2.5 years and my life has been completely changed. I no longer have a cell phone service, use microwave, have WiFi in house. I sleep with circuit breaker off in my room. I have less friends now that I am not the most convenient person to hang out with. I can still be in touch by email, Facebook, home phone. Just not by cell phone or text message.
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Fatigue with electromagnetic hypersensitivity

My condition is improving and I am getting less debilitating headache, I am more aware of other physical conditions. I have been very fatigue when I have EMF exposure and I often drink coffee just to get enough energy. I have good days and bad days and it is constant yo yo like life that never ends.
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Neighbor illness – Lyme Disease and Compadre

I just watched a story of a man (Xiren) who is recovering from Lyme disease on youtube. The video is well made, because he is in the music industry (great music) and shows great editing skills. His health journey is different from mine because of different illness, yet there is some similarity in struggle. He did not have the diagnosis right away, had suicidal thought, experimented with different treatments and supplements. What I really liked him saying was that he said that no one will understand what you are going through. I can totally relate to that and I felt that it is a solo battle and a journey. Even friends and families will not understand what I am going through, and I need not to expect them to understand. I think the reason Lyme disease and EMF Hypersensitivity is kind of similar is because they both mess with one’s nervous system. When nervous system is messed up, you cannot think straight and function correctly. I hope he will be completely cured soon and end his journey. Be well and Get better.

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Update

It helps to write a blog so I can keep track of my progress and it should give the readers my progress. My daughter had enrollment ceremony on Saturday so I attended. People are taking pictures and videos with their cell phones. Also, hall way had fluorescent lights. I was not sure if the class room had fluorescent light or LED. I then had an appointment of teeth cleaning. After I came from, I had plumber come over for water filter replacement. He showed me a picture of his daughter on his cell phone. With all that activities and exposure, I did OK. I still tried to sit away from people and keep a distance as much as possible when people are using cell phones. I had 2 eon lifewave patches on Saturday.
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2 Years EHS Anniversary

I have had 2 year anniversary. When I became ill, I did not know how long I was in it for or if I was going to get any better. I became worse every day for long time. It almost felt like rolling down the hill and there is no sign of recovery in sight.

I have found that there is no single cure like a magic bullet. I am on the healing journey. Although my condition is improving, there is no guarantee that I will one day completely be cured or when I am going to be cured. The recovering is not linear and there is occasional unexpected hick ups.

My sensitivity has gradually decreased over time. I can be in the environment that is not EHS friendly for longer without getting the headache. Most of days, I do not have headache. I get tingling (buzzing) sensation on the head but it does not turn into headache. I do get drained when I have more exposure to EMF/RF. I still have irritability but not as much as before.

I can give gratitude now. During the suffering, I could hardly give gratitude. I could conceptually give gratitude but I could not feel the gratitude, because the life was suffering. I am regaining my confidence back.

I have lost so much in the suffering such as money, time, friendship, fun, connection and etc, but I have gained health knowledge and desire to improve quality of life.

I kept working, held on to a job and supported my family in this difficult tragedy and I am proud of that. No one can understand what I went through even people with EHS can, because everyone’s life is unique. I am just going to continue with my course and see what life takes me to.

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Attended 4 day seminar

I had an opportunity to attend personal development seminar in my home town. The cost was bare minimum although I had to take off work for 2 days.  I had concern about seminar’s fluorescent light if any and cell phones from people who are attending the seminar.  I am happy to say that I have completed the seminar and now I know that I can attend seminars, go to movie theater and etc. My world just has expanded.

The hall way had lower ceiling and compact fluorescent lights. I avoided the hall way by going to a balcony and hang out there. I also avoided going near people who are talking on the cell phone or texting. I tried to sit on the end of the row near the wall. I put 2 lifewave’s eon patch every day.

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Fluorescent lights causing headache

I listened to interview Dr. Richard Conrad and he says that fluorescent lights and computer monitors emit flickers and some people are sensitive to the flicker. It is called “Flicker sensitivity”. I am very sensitive to fluorescent lights myself. I think there is more to fluorescent lights than just flickering. Most likely fluorescent light ballast emit some kind of frequency that cause headache in my case.

I have had few interesting incidents that relate to this:

  1. I was at acupuncture office after developing severe headache. Main office had fluorescent lights. I was in the treatment room that had over head fluorescent lights off. I also closed my eyes entire time I was being treated. I gradually got headache even though my eyes were closed.
  2. When my condition was very bad, I could not go into shops that have over head fluorescent lights. I often parked my car in the parking lot and waited for my wife to finish shopping. When I parked my car in front of the shop, I often got headache even though I was not looking directly into the store.
  3. I had electrician replace in ceiling fluorescent lights with incandescent/LED type in ceiling lights. When the fluorescent lights were removed but ballast still connected, he turned on the switch and I got zapping headache when he did that.
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