Elderly Man with EHS Abused by Hospital and Nursing Home
by Lisa Bryngelson (translated from Swedish)
This is a disturbing story about how an
elderly man with electrical hypersensitivity was mistreated by the medical and
social system.
Keywords: |
Aging, senior citizen, elderly, social
services, hospital, assisted living, nursing home, electrical
hypersensitivity, electrical sensitivity, accommodation, abuse |
Elderly people with
electrical hypersensitivity (EHS) who are institutionalized are made to suffer. The personnel is
supposed to listen to people with disabilities and try to accommodate their
needs and wishes, but who listens to someone with electrical
hypersensitivity? Nobody listened
to Kalle.
Kalle fell on the floor
of his home. As far as I know,
this was the first time it had happened in his old age. He was so unfortunate in that he landed
between the sofa and the wall and couldnÕt get up on his own.
He had to lie there for
hours until he was found by his son. The son didnÕt believe in EHS and would
not listen to Kalle; instead he called for an ambulance and Kalle was taken to
the emergency room. From there he
was admitted to the hospital.
Kalle wanted to get home again, but then he heard the words Òforced
hospitalizationÓ.
Kalle was able to move
around the hallways using a walker for the first few days, but then he became
unable to walk. The high radiation
(EMF) level in the hospital paralyzed his legs. He now had to sit in a wheelchair.
The medical tests could
not explain why Kalle had fallen in his home. After a week in the hospital, he was told he would be
allowed to return to his home and receive assistance from the social
services. He met with a social
worker, whom he told he had EHS and that he needed the
social services to accommodate that.
He thought the social worker made a note about the issue.
Kalle was able to walk
again when he returned home. He
walked on his own legs from the car and up the steps to the porch and into his
home. He was overjoyed when he
called me on the phone and told me that now he could walk again. Now he wanted to exercise his legs.
A nurse showed up while
we were talking, so we ended our conversation. What did the nurse do?
Did she listen to Kalle? She
brought along a wireless monitor, which she fastened around his wrist. Kalle protested, explaining he had EHS
and did not tolerate such a wireless device. He had to have it, the nurse replied. Kalle sat in a chair in the kitchen,
and there he continued to sit, as he was not able to walk with the monitor on
his wrist. ÒShe was not nice,Ó
Kalle later said about the nurse.
The next day a man showed
up and started to drill a hole in KalleÕs front door. Kalle was still stuck in his kitchen chair and could not
walk, so he shouted ÒWhat the hell are you doingÓ to
the man.
The man replied that he
was installing a wireless door lock, so the nurse could open the door with her
cell phone. Kalle replied that he
didnÕt want this new lock, as he did not tolerate wireless things. He had to have it, the man replied, and
he installed the lock.
Kalle was stuck in his
chair. He received visits by the
social services morning, noon and evening. He was left alone to eat the meals they brought, even though
it was difficult for him to eat and swallow his food. He used the wireless monitor on his wrist to get help, but
that taxed the social services so much they moved him to a nursing home.
The EMF radiation levels
were higher in the nursing home.
The dining hall was the worst, with all the cell phones, electric
wheelchairs and hearing aids.
Kalle had even more trouble swallowing his food, so it was almost
impossible for him to eat. He
could eat yoghurt. He asked to eat
in his room, but that was denied.
Kalle was plagued by
dizziness, headaches, various pains and simply feeling poorly, due to the
electrical environment in the nursing home. He had problems sleeping, eating and drinking. Nobody cared. Kalle wanted to get home, that was
better than the nursing home.
Kalle was not allowed to move back home.
ÒThat I should end up in
such a bad situation!Ó he said. He
just wanted to die.
Finally, he was allowed
to move back home. Of course, he
had to live with the wireless monitor and door lock, and not enough assistance,
but he came home. His health was
now much worse after living in the nursing home. He died not long after returning home.
KalleÕs obituary says
that gifts to cancer research are welcome. But wait, it was EHS that was the problem! Even in death, his illness is ignored.
There are many like Kalle
— suffering, ignored and finally destroyed by an environment they cannot
live in. You and I are next. How long do we have to be silenced and
ignored? We must raise our voices
to stop these abuses.
This story is written by Lisa Bryngelson, who was KalleÕs friend and next door neighbor. The story was first published in the 2013/3 issue of Ljusglimten, which is a magazine from the Swedish EHS organization. This English translation is made with Lisa BryngelsonÕs permission.
Responses to the story
In the following issue of Ljusglimten (2013/4), the editor reports receiving many responses to the story about Kalle. Two of the responses were printed, including one from Jan Hanes, who visited Kalle a few days before he died. He mentions how weak Kalle was, and generally supports Lisa BryngelsonÕs account of KalleÕs story. He comments that he knows four women with EHS who live in elder-housing and who are treated as poorly as Kalle was. He also knows a woman who had to flee to her uninsulated vacation cabin during winter, and who later died shortly after a 3G cell tower was erected nearby.
TranslatorÕs comments
This story takes place in Sweden, but the problem is global, and likely to become worse as the first generation of people with EHS is aging and more wireless gadgets are introduced.
I inquired about the story and learned that none of KalleÕs friends know the direct cause of death, but it is unlikely to be cancer that killed him.
The wireless monitor they put on KalleÕs wrist allowed him to press a button to call for help. The device transmits continuously, so the social services know it is working properly. It might also inform them of his location.
One naturally wonders why Kalle didnÕt refuse the monitor and didnÕt stand up to the authorities more than he did. In some of the European countries, the culture is that people do what they are told by authority figures. This is a concept that is rather alien to the American culture, though even in America the medical system can exert a lot of control over its patients. If Kalle had lived in the United States, the story would probably not have ended any better.
The article Prescription for Abuse by Jan Goodwin in the July-August 2014 issue of AARP Bulletin describes how nursing homes in the United States routinely drug patients into submission, simply because it is convenient for the staff — a staff which is generally overburdened and undertrained in order to maximize profits. The article quotes Charlene Harrington, professor at UCSF, that this is done to as many as 20% of the nursing home residents in the United States. Being drugged into oblivion probably does not reduce the health effects of EMF.
Also, in America, a person refusing to comply with monitoring devices and other insults may simply be given the choice between going along or be left with no help at all. People there do not have the same rights to social services as is the case in Sweden.
2014