Man Traveled by 2 Planes and Was in Two Airports Traveling to Boise, Then Found Dead at Home, Anthony Fauci at NIH Seems to Have a Knowledge Defecit About COVID 19, Not Surprised, I have ME/cfs, He's Helped Block Research. We Know About Him Already. For COVID 19 Info Dr. John Campbell, Nurse Educator is A#1.

A couple days ago I called the health department here in Boise because there was an article in the news describing how a man who had been in China got on a plane to fly to the US. He then must have gotten on another plane to fly to Boise. The woman tried to divert my attention away from my concerns by mentioning irrelevant things and telling me the man just stayed at his house. I said, he flew from China, was not quarantined, then got on another plane to fly to Boise, that's two airports and two airplanes. What kind of transport was used to get him from the airport to his home, a taxi or shuttle bus, did someone pick him up?

Hawaii announces its coronavirus tests from the CDC were faulty, and it points to a major gap in treating and stopping the spread of the virus

 

There are other reports of issues with the test here and in China. I was already familiar with the CDC staff who invent tests that do not work, patent them and then make millions based on the science their agency works on, but the tests often do not even work well, corruption at the CDC abounds. The Lyme test is one of those scams. My rheumatologist in Seattle was a professor at U of W and treated me for Lyme Disease based on symptoms stating the test was crap. 

In the past I thought the cover up was due to a cover up of an illness I have, ME/cfs was about vaccines or bioweapons. We know the outbreak of Lyme Disease on the east coast is due to Lyme being used as a bioweapon. In fact the man the pathogen was named for, Willy Burgdorfer was working a a project to put several pathogens at one time into ticks so they could weaponize ticks. The multiple pathogens was to cause people to be ill with several infecting them and massive symptoms making figuring out what they had impossible to spread panic in the population and take out part of those needed to mobilize for war. The ticks were somehow unleashed upon us. Now I believe there are many causes of ME/cfs. There is also a theory that it is really AIDS and the AIDS epidemic was manipulated to demonize gay men while the rest who have it are being treated like shit by their country and the medical community as well. Considering the corruption involved in the HIV research who knows what the truth is.

I am a DES Daughter and that has been massively covered up to the point of the drug companies stopping medical schools from even teaching about it. They only allow the info about the genito-urinary abnormalities it causes in utero, not that it caused genetic alterations of our whole bodies including our immune systems. In the 1970s I was involved in a group lawsuit with Belli, Ashe and Coulos (spelling?) in San Francisco. It was to be the precursor to class action. Melvin Belli's lawfirm fucked us. They suddenly made us our own lawyers sending certified letters the day before hearings we did not even know about. It was

massive malpractice. Then there were fake articles in the newspaper to divert us from thinking we could sue Eli Lily et al due to the massive damage they had done to us for profits. About three months before this I was gang raped at the home of one of the sons of the man who owned the Chinese Wax Museum. It has taken me decades to connect those dots because in the 70s or 80s or even 90s who could have imagined weaponized gang rape designed to traumatize someone. After being a nurse in Nome Alaska I can. But back then I could not have imagined what my government really is or that they would be perpetrating a holocaust upon their own people in the form of organized stalking/harassment, militarized police, directed energy weapons or forced homelessness.  John Kalin were you paid off by Eli Lily or a big pharma group? I believe the DES is what caused the ME/cfs, the problems with my immune system and much more. And all the trauma has contributed to my health issues. Evil runs the United States.

There was no justice for the gang rape, there is never justice for poor people against the wealthy. I was a political science student at San Francisco State also working which I did the whole time I went to college. My plan was law school because people were talking to me about getting into politics because, "You will never lie to the people." That is true, but I was very shy at that time. My plan was Poli Sci, then law school hoping that would cure my shyness. I could stand up and speechify like mad, but working in groups I shut down. Was like that as a child too.

The San Francisco Police Department laughed when I told them where the rape by 8 or 9 men happened. They refused to file a police report. Is this when the targeting began because I have had police refuse police reports for decades of intentionally caused accidents, harassment, rape and more? Is it a contractor working for Big Pharma? I was told in the 1990s St. Joseph's Hospital had put me on some list for being a trouble making nurse. Considering the psychopathic CEO they had hired to go after the excellent and strong nurses at that hospital nothing would surprise me. Is that when it started, this is when a series of intentionally caused car accidents happened. Oh yea, then there was the known pedophile priest they had on staff, thanks for covering that up and making us all work with the bastard that traumatized girls in Nome Alaska before coming to Tacoma. Strange things have happened for decades, but the organized part started in Nome Alaska, but right around then is when they were organizing the gangstalking out of the fusion centers. Before that the police in Deming NM gangstalked me like Texas did to the witnesses of the JFK assassinations when I reported to the chief cops were dealing drugs and I whistleblew about my employer committing medicaid fraud. I had no idea how bad either situation really was and two good cops warned me my life was in danger. It was years before I found out the whole stories.

This whistleblower was not me as I was not looking to make millions, just like in Nome Alaska I reported the problems to the appropriate agencies many years before it was in the news. I reported it to everyone, legislators, the DA, all appropriate agencies and not a one of them did their damn jobs. Then years later this info below happened. The bastards I was working for still are on my blog every now and then. Why? Wondering what I have figured out so far?

Community Health Systems to pay $75 million in Medicaid fraud whistleblower case

Suit claimed the hospital operator illegally donated money to New Mexico counties in return for higher Medicaid payments. 

This is their latest appearance. It is odd that what they are looking at is about the Palins now isn't it? Is there a connection?

My country fucked me before I was even born with DES, then covered up the truth about it to this day and made sure we could not get compensated. They lie about us our whole lives. We are medically bullied due to medical ignorance by design. People with ME/cfs are medically bullied as lies have been told about the disease for decades and the lives of three scientists were ruined for doing real research and trying to help us. Then year after year I get fucked over again and again. The problem is the corporations are in charge, the oligarchy has taken over everything. It did not recently happen, I was born in 1955. What is going on now is the internet allows people to find the truth about many things.

Through my life experiences I know just how evil those in charge of the government are on every level. I know how incompetents are running everything because the agenda is not skill, education or experience, it's willingness to fuck the public and do evil for the overlords. I learned my first lesson in this from watching Sarah Palin.  

Yesterday Cynthia McKinney posted this. Anthony Fauci at the NIH is very well known to those in the ME/cfs and AIDs communities. He propagandizes the public and manipulates the medical thinking about ME/cfs preventing us from getting appropriate research. He helped demonize us, tried despite thousands upon thousands of research articles to make ME/cfs into a psychiatric problem. Psych problems do not cause the massive physical issues we have, they don't cause immune system dysfunction of the immune system you tool of the oligarchy.

This is the problem, this virus is contagious before anyone even realizes they are ill. Fauci is an idiot. But he isn't in place to protect the public, no, his job is propaganda and subversion of the truth for the NIH.

Then yesterday this. 

 

Coronavirus Updates: Cruise Ship Passengers, Some Infected, Flown Back to U.S.

As passengers were released from a ship in Japan, health officials scrambled to test travelers from another ship, in Cambodia, after one person who had left was found to be infected.



Then today.

Why did US break Diamond Princess coronavirus quarantine? 'Something went awry'

Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases at the National Institutes of Health, said the original idea to keep people safely quarantined on the ship wasn't unreasonable. But even with the quarantine process on the ship, virus transmission still occurred.

No shit Sherlock. Cruise ships are the worst places on the planet for spread of disease. The windows in many of the lower cost cabins do not even open. They use air conditioning instead which spreads the virus. You know like those blowers do in public bathrooms or the air systems in airplanes. How would the NIH not know just exactly what was going to happen? How can they not quarantine people during an outbreak?

They based the decision to transport people on if they had symptoms or not. How the hell could they use that criteria when it is known COVID 19 is contagious when there are no symptoms?  HHS was also involved in this.

88 more coronavirus cases found on Diamond Princess cruise ship

 

 I’d like to sugarcoat it and try to be diplomatic about it, but it failed,” Fauci told USA Today. “People were getting infected on that ship. Something went awry in the process of the quarantining on that ship. I don’t know what it was, but a lot of people got infected on that ship.”

 Yes, something did go awry, dumbassery. But at least now you have been exposed. 

Through all of this who is the best source of information? That would be Dr. John Campbell, a Phd nurse educator in the UK. His videos have been not just very educational but also designed to dispel conspiracy theories and misinformation. Below is one of the videos he made today.

We still do not know the cause of death of the man who flew from China to LA, then on to Boise and died in his home. 

The ME/CFS Worldwide Patient Alliance Puts a Half-Page Ad In WAPO

Remember, the FDA which is the agency that regulates blood banks has know for decades that many scientists were certain Myalgic Encephalomyelitis/Chronic Fatigue Syndrome or ME/CFS was caused by a retrovirus. When I was a supervisor at a blood bank in the 1990s in Tacoma WA we did not allow people with ME/CFS to donate. Why is it we could get to the information to make that decision yet the FDA couldn't?


-Possible New HIV-like Retrovirus in Blood Supply--



CORAL GABLES, Fla., Dec. 6, 2010 /PRNewswire-USNewswire/ -- In an unprecedented move, chronic fatigue syndrome (CFS) patients published a half-page ad in The Washington Post today. The ad brings attention to new, HIV-like retroviruses, including XMRV, which have been linked to CFS and aggressive prostate cancer, and have been detected in healthy blood donors.


The ad was created through the ME/CFS Worldwide Patient Alliance (MCWPA), a grassroots patient collaboration formed in August 2010 with the support of P.A.N.D.O.R.A., Inc. From their beds and wheelchairs, patients spent decades watching researchers, scientists and physicians debate about the cause or nature of their illness. Now, they are adding their voice through a campaign that calls for biomedical research funding, fast-track treatment options and improved patient quality of life. CFS, also known as myalgic encephalomyelitis or ME/CFS, is a disabling, sometimes fatal NeuroEndocrineImmune disease that afflicts more than one million Americans and an estimated l7 million people worldwide.

ME/CFS first gained national attention amidst the AIDS epidemic in the early 1980s. As early as 1991, a retroviral link to ME/CFS was discovered by Dr. Elaine DeFreitas of the Wistar Institute, but subsequent retroviral research was halted by the government. Although more than 4,000 peer-reviewed articles in medical journals have pointed to system-wide immune, neurological, endocrine, gastro-intestinal and cardiac abnormalities, a biologically-based diagnostic definition has eluded doctors. The result has been a catastrophic lack of care, ineffective (sometimes harmful) treatments and a shorter life span for those who are ill. The leading causes of death among patients are heart disease, cancer and suicide. The disease occurs in people of all ages, from children to seniors, and also has a higher incidence rate in families and has occurred in cluster outbreaks.


"This can happen to anyone," said Sita G. Harrison, spokeswoman for the MCWPA. "ME/CFS is devastating and the lack of care has hurt us all. We ask the government and health care agencies that we put our trust in to help the millions of people who are suffering and to fund more research now."


A major scientific breakthrough occurred in October 2009 when the Whittemore Peterson Institute (WPI) at the University of Nevada, Reno, working with the National Cancer Institute and Cleveland Clinic, published the results of a landmark study. The seminal study, published in the leading scientific journal, Science, discovered the third human retrovirus, XMRV, in the blood of 67% of ME/CFS patients and in 3.7% of healthy controls. This suggests that up to 10 million US citizens could already be infected. This finding was later confirmed by the FDA, NIH and Harvard Medical School in a study published in the Proceedings of the National Academy of Sciences. Their results linked a family of human gamma retroviruses (to which XMRV belongs) to ME/CFS at a rate of 86.5% and 6.8% in the healthy population, bringing the total of Americans who may be infected up to 20 million people.

The CDC and NIH have spent thirty years trying to prevent the cause of this disease from being found. I want to know why. They also gave it a silly name in the U.S. so it would not be taken seriously. If anyone knows anything about how the drug companies manipulate physicians they know they are also easily manipulated by government agencies as well as the AMA. Not only do the lies and diverting of research funds need to end, the abuse perpetrated on the people suffering from ME/CFS by physicians needs to end. Some of them will have to be forcefully educated by regulating agencies because many of them choose ignorance. A large part of the suicidal incident which got me arrested and the medical abuse I received in Nome was due to Chronic Fatigue Syndrome. When I got PTSD the cortisol that is released causes the virus to reproduce and be released by cells in the immune system. I became very ill. This causes "brain fog", in other words it is difficult to even think or make appropriate decisions at times. Coupled with the severe PTSD from the workplace bullying I was very disabled. When I tried to get help the doctors refused and were very abusive. Of course this was not just due to prejudice against ME/CFS, this was also due to the lies spread by the two levels of workplace bullies at the hospital in Nome. This disease is very complicated and has a lot of unusual symptoms, many doctors can't comprehend this for some reason. We are all thankful for the ones who do and the ones who even though they did not know what to do for us tried as best they could, being believed is very therapeutic. Being very ill and treated as if you are just imagining it contributes to the suicide of ME/CFS patients.


"The NIAID, the national institute responsible for infectious disease research, has yet to fund XMRV research in ME/CFS or any other disease," explains Annette Whittemore, President of WPI. "WPI has had its last six XMRV-related grant proposals turned down; despite the fact that our researchers have proven XMRV is transmissible and infectious."


MCWPA is advocating for a budget that is in line with other NeuroEndocrineImmune diseases. Currently, only $5 million for ME/CFS research is in the NIH budget, far less than similar diseases such as multiple sclerosis ($l44 million) and lupus ($121 million). Patients also ask for antiretroviral and Ampligen clinical trials that have shown great promise in mitigating the effects of ME/CFS.


For more information, to donate, or for more resources and spokespeople, including leading researchers, scientists, physicians, patients, and historians please visit http://mcwpa.org/.


About MCWPA: Our mission is to create an effective, cutting-edge advertising campaign addressing the poor quality of life of individuals with ME/CFS. By issuing a collective and unified statement, our community will no longer be silent and invisible. The MCWPA ad campaign is supported by P.A.N.D.O.R.A. Inc.™, Vermont CFIDS Association, Inc., R.E.S.C.I.N.D., Rocky Mountain CFS/ME and FM Association and the Wisconsin ME/CFS Association, Inc.
Emphasis added by myself.

Is some drug company wanting the cause kept secret as they develop a drug and don't want competition from other drug companies? Did the government block research, appropriate diagnosis, treatment and prevention to keep people for getting Social Security disability, Medicaid and Medicare? Were these viruses spread through vaccines or some military germ warfare experiments? Somehow somewhere there has to be a reason for intentionally harming a very large number of people while allowing virus to spread that is more logical than cruelty, prejudice and group stupidity for thirty years.

Here is a list of some of the symptoms of ME/CFS from the CFIDS Association (Chronic Fatigue and Immune Dysfunction Syndrome):

Symptoms



Although its name trivializes the illness as little more than mere tiredness, chronic fatigue syndrome (CFS), also known as chronic fatigue and immune dysfunction syndrome (CFIDS), brings with it a constellation of debilitating symptoms.

CFS is characterized by incapacitating fatigue (experienced as profound exhaustion and extremely poor stamina) and problems with concentration and short-term memory. It is also accompanied by flu-like symptoms such as pain in the joints and muscles, unrefreshing sleep, tender lymph nodes, sore throat and headache. A distinctive characteristic of the illness is post-exertional malaise, a worsening of symptoms following physical or mental exertion occurring within 12-48 hours of the exertion and requiring an extended recovery period.

The symptoms of CFS are highly variable and fluctuate in severity, complicating treatment and the ill person’s ability to cope with the illness. Most symptoms are invisible, which makes it difficult for others to understand the vast array of debilitating symptoms with which people with the illness must contend.

Other Common Symptoms

I have highlighted the ones I have had or have now, the symptoms change over time.


Additional symptoms are reported by people with CFS (PWCs) such as word-finding difficulties, inability to comprehend/retain what is read, inability to calculate numbers and impairment of speech and/or reasoning. PWCs may also have visual disturbances (blurring, sensitivity to light, eye pain, need for frequent prescription changes); psychological problems (depression, irritability, anxiety, panic attacks (only after the PTSD), personality changes, mood swings); chills and night sweats; shortness of breath; dizziness and balance problems; sensitivity to heat and/or cold; alcohol intolerance;  (abdominal pain, irregular heartbeat; irritable boweldominal pain, diarrhea, constipation, intestinal gas); low-grade fever or low body temperature; numbness, tingling and/or burning sensations in the face or extremities; dryness of the mouth and eyes (sicca syndrome); gynecological problems including PMS and endometriosis; chest pains; rashes; ringing in the ears (tinnitus); allergies and sensitivities to noise/sound, odors, chemicals and medications; weight changes without changes in diet; light-headedness; mental fogginess; fainting; muscle twitching; and seizures.

There are many other symptoms, some of them are strange like temporary loss of fingerprints. For years I had excrutiating pain everytime I took a breathe, my feet hurt so bad I had a hard time walking, I had severe diarrhea, severe headaches, crazy shifting sleep patterns, restless leg syndrome (and restless whole body sometimes) swelling of my legs and I was very dizzy, but I did everything I could to continue to work. Sometimes I had to cut back to part time or rest a few weeks, going back to full time as soon as I could. I would have episodes of vomiting/diarrhea that would last for hours until I tore my esophagus and ended up in the hosptial. Many of the medications they gave made the dizziness worse. They did not know then we are almost a pint low on blood, so gave meds that exacerbated the problem. The doctors would tell me it was something insignificant and my coworkers would tell me they were wrong because I looked like crap and had weird symptoms. I had a low grade fever for years. We had a rule that if a patient in the ICU had a fever that was not higher than mine we did not call the doctor because there I was working with a higher fever. The running joke was that I was sicker than a lot of the patients. The PTSD from the workplace bullying did me in, otherwise I would have kept working. Of course being a nurse put me in danger due to the immune system problems, but doctors told me this was not true, so I caught one virus after another and had severe constant pulmonary/sinus infections. It was the antibiotics that caused the severe diarrhea.

Now even though my sleep is still crazy I can sleep when I can. I am eating an extraordinarily healthy diet and taking lots of supplements. XMRV and the other mouse retroviruses associated with CFS cause cancers, especially lymphoma and prostate, this is one reason for the diet change and supplements, giving my body what it needs to mount a defense against cancer. I have taken supplements for years for this reason and was unable to take them while homeless and struggling to find a way to survive on social security, that put me in a lot of danger. I take no meds except an OTC allergy pill. I have researched what foods cause pain and which prevent it and this has helped my comfort level immensely. I have been able to figure a way to get exercise by doing it periodically while I am awake. It took years for me to even be able to read much after what happened in Nome as well as the wrongful imprisonment, harm to my cat, theft of my property (No justice for any of it) severe abuse in the prison system and homelessness (BTW, they told me CFS isn't a real disease at Hiland Mountain, so they refused to treat it). I normally read and did research all the time, so it was very depressing to have my brain not work for years. Now I am generally reading tons of articles on line every day and several books at a time.

I feel much better and my brain functions on a higher level. I look very different now and have lost weight. I did this by myself, every doctor I have seen in Alaska knows nothing about ME/CFS or is abusive to me because they don't think it is real. I had an MRI in Homer only because I insisted due to neurological symptoms so bad I looked like I had MS. It showed brain lesions which is exactly what I suspected. The doctor told me the MRI was normal and tried to block me from reading the report. After reading the report I made an appointment with a neurologist who after testing told me she could not say I don't have MS. Now, she knew I have CFS which can look identical to MS and CFS brains can have lesions. Her diagnosis was the brain lesions were caused by my headaches. I told her I was not buying the headache theory. This was after she insisted I have a sleep study to rule out sleep apnea when CFS and Aspergers both carry erratic sleep problems. I am on my own completely with this. I am thankful to all the scientists, physicians, organizations and patients who post information I have been able to use to get healthier. The PTSD has gotten better, but incidents coming up in the future could trigger the retrovirus. It is my hope that my body will be stronger and I will tolerate the flare up better. Now that I can get enough sleep by just sleeping when I can my immune system should function better.