Related to the last post, I’ve been thinking about when my symptoms first appeared.
1994– Amalgams (metal dental fillings with up to 50% mercury content) placed. I think it was four, but I ended up with 9! After my divorce, in 1994, my teeth took a downward spiral. Never had any problems until then. I think this is important when I realized both of my dentists were members of the secret society of my small hometown.
1995–First experienced terrible monthly migraines lasting 3-5 days. They always came with my period, so I assume they were related to my hormones. But that was a part of the puzzle. Mercury is a heavy metal and impacts every organ in the body and causes brain toxicity. That’s why it is also a factor, but perhaps the parasites were the root cause, as cerebral malaria causes migraines, chills, lethargy. All of the symptoms I was experiencing.
1992-2000 — Bill and Hillary Clinton were in the White House. I know by their reactions to my discovery that I am on target about cerebral malaria and they had something to do with it. I also had a vision of the Rothschilds’ anger at my discovery.
Since my symptoms began after the immune devastating mercury poisoning, that it is likely the symptoms I have experienced were malaria. God Bless my Helpers whom have continually helped me to put the puzzle together. Everything happens in its own timeline.
My fatigue was so bad at the worst of it — 2007-2013 — that I could barely walk 20 feet without feeling extreme fatigue. My adrenal glands were exhausted from trying to support my beleaguered system. At one point in time, I had adrenal exhaustion so bad that I nearly collapsed as I was trying to get back to bed after using the restroom. My legs gave out just two feet from the mattress and I literally threw myself into bed before my legs gave out. This was a medical emergency. Your adrenal glands are very important and if your body is besieged with toxins, it is on overload and you can die from adrenal collapse. I found out that I could support my adrenals by using a tiny bit of hydrocortisone to support them. When I say tiny, I mean tip of your little finger. It is a tricky thing, because you can get too much hydrocortisone and then your body is no better off as the adrenals are very, very touchy.
I was a substitute teacher during this period and remember having to lie down at the lunch recess so that I could teach the entire day. I nearly collapsed a few times while teaching and had to teach from a sitting position.
Once I chelated most of the mercury out, I no longer needed the hydrocortisone. I was glad to be off of it because it was costly and I hate taking anything.
Because of the extreme fatigue, I thought perhaps I had chronic fatigue. I knew the mercury was a factor, but with the new revelation of the cerebral malaria, I started looking at the symptoms of chronic fatigue.
From the wiki:
Persons with CFS may recover or improve over time, but some will become severely affected and disabled for an extended period.[
Cognitive dysfunction is one of the most disabling aspects of CFS due to its negative impact on occupational and social functioning. 50–80% of people with CFS are estimated to have serious problems with cognition.[38] Cognitive symptoms are mainly due to deficits in attention, memory, and reaction time.
Many, but not all people with ME/CFS report:[15]
Increased sensitivity to sensory stimuli and pain have also been observed in CFS.[
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Evidence points to abnormalities in the hypothalamic-pituitary-adrenal axis (HPA axis) in some, but not all, persons with CFS, which may include slightly low cortisol levels,[65] a decrease in the variation of cortisol levels throughout the day, decreased responsiveness of the HPA axis, and a high serotonergic state, which can be considered to be a “HPA axis phenotype” that is also present in some other conditions, including post-traumatic stress disorder and some autoimmune conditions.[66] It is unclear whether or not decreased cortisol levels of the HPA axis plays a primary role as a cause of CFS,[67][68][69] or has a secondary role in the continuation or worsening of symptoms later in the illness.[70] In most healthy adults, the cortisol awakening response shows an increase in cortisol levels averaging 50% in the first half-hour after waking. In people with CFS, this increase apparently is significantly less, but methods of measuring cortisol levels vary, so this is not certain.[71]
The symptoms of chills and lethargy associated with CFS are too similar to cerebral malaria to be dismissed.
And this is the timeline:
- From 1934 onwards, outbreaks of a previously unknown illness began to be recorded by doctors.[137][138] Initially considered to be occurrences of poliomyelitis, the illness was subsequently referred to as “epidemic neuromyasthenia”.[138]
- In the 1950s, the term “benign myalgic encephalomyelitis” was used in relation to a comparable outbreak at the Royal Free Hospital in London.[139] The descriptions of each outbreak were varied, but included symptoms of malaise, tender lymph nodes, sore throat, pain, and signs of encephalomyelitis.[140] The cause of the condition was not identified, although it appeared to be infectious, and the term “benign myalgic encephalomyelitis” was chosen to reflect the lack of mortality, the severe muscular pains, symptoms suggesting damage to the nervous system, and to the presumed inflammatory nature of the disorder. Björn Sigurðsson disapproved of the name, stating that the illness is rarely benign, does not always cause muscle pain, and is possibly never encephalomyelitic.[137] The syndrome appeared in sporadic as well as epidemic cases.[141]
- In 1969, benign myalgic encephalomyelitis appeared as an entry to the International Classification of Diseases under Diseases of the nervous system.[142]
- In 1986, Ramsay published the first diagnostic criteria for ME, in which the condition was characterized by: 1) muscle fatiguability in which, even after minimal physical effort, three or more days elapse before full muscle power is restored; 2) extraordinary variability or fluctuation of symptoms, even in the course of one day; and 3) chronicity.[143]
- By 1988, the continued work of Ramsay had demonstrated that, although the disease rarely resulted in mortality, it was often severely disabling.[2]: 28–29 Because of this, Ramsay proposed that the prefix “benign” be dropped.[139][144][145]
Chronic fatigue syndrome[edit]
- In the mid-1980s, two large outbreaks of an illness that resembled mononucleosis drew national attention in the United States. Located in Nevada and New York, the outbreaks involved an illness characterized by “chronic or recurrent debilitating fatigue, and various combinations of other symptoms, including a sore throat, lymph node pain and tenderness, headache, myalgia, and arthralgias“. An initial link to the Epstein–Barr virus had the illness acquire the name “chronic Epstein–Barr virus syndrome”.[2]: 29 [86]
- In 1987, the CDC convened a working group to reach a consensus on the clinical features of the illness. The working group concluded that CFS was not new, and that the many different names given to it previously reflected widely differing concepts of the illness’s cause and epidemiology.[146] The CDC working group chose “chronic fatigue syndrome” as a more neutral and inclusive name for the illness, but noted that “myalgic encephalomyelitis” was widely accepted in other parts of the world.[86]
- In 1988, the first definition of CFS was published. Although the cause of the illness remained unknown, several attempts were made to update this definition, most notably in 1994.[85]
- The most widely referenced diagnostic criteria and definition of CFS for research and clinical purposes were published in 1994 by the CDC.[51]
1934 was the first recorded notes of the affliction. This was post World War I. Important to note that. Remember, the Rothschilds funded every war since the Revolutionary War here, in the United States, and who knows how many worldwide.
Since we know the Third Reich was purposely using malaria as a bioweapon during World War II, it is likely that WWI was the precursor of their evil plans.
Since the Rothschilds are satanists, the likely targets are Good Hearts who are kind, compassionate, generous, honest. But that doesn’t mean those that join them are going to be let alone. If you’re not part of the Dark Nobility, you’re a target, too. But they need humans to do their dirty work so they look like fine people. That is the way of evil ones. They get others to do the killings and such and think that they will not pay for it when Judgment day comes. Oh, I beg to differ. The Creator is very patient, however, and truly wants everyone in Heaven, but the Creator has a limit, as we saw with Noah. People were marrying and partying up until the floods came.
All for now. I’ll keep researching this, however.
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