Flumist is a Biological weapon! Crosses Blood Brain Barrier and destoys your cells!
"...Overcoming the difficulty of delivering therapeutic agents to specific regions of the brain presents a major challenge". Blood-brain barrier - Wikipedia, the free encyclopedia
*H1N1 Flumist has overcome this obstacle as the "weapon of choice".
The blood-brain barrier (BBB) is a separation of circulatingblood and cerebrospinal fluid (CSF) maintained by the choroid plexus in the central nervous system (CNS). Endothelial cells restrict the diffusion of microscopic objects (e.g. bacteria) and large or hydrophilic molecules into the CSF, while allowing the diffusion of small hydrophobic molecules (O2, hormones, CO2). Cells of the barrier actively transport metabolic products such as glucose across the barrier with specific proteins.
The blood-brain barrier acts very effectively to protect the brain from many common bacterial infections.
Thus, infections of the brain are very rare. However, since antibodies are too large to cross the blood-brain barrier, infections of the brain that do occur are often very serious and difficult to treat.
The blood brain barrier becomes more permeable during inflammation however, meaning some antibiotics can get across.
Viruses easily bypass the blood-brain barrier by attaching themselves to circulating immune cells.
*The H1N1 contains a live virus which attaches itself to circulating immune cells throughout the mucusa membrane using the flu mist.
Transport mechanism *Flumist and injection
Mechanisms for drug targeting in the brain involve going either "through" or "behind" the BBB. One such strategy to go through the BBB may entail the use of endogenous transport systems, including carrier-mediated transporters such as glucose and amino acid carriers, receptor-mediated transcytosis for insulin or transferrin.
Transferrin is a blood plasmaprotein for iron ion delivery.When a transferrin protein loaded with iron encounters a transferrin receptor on the surface of a cell (e.g., to erythroid precursors in the bone marrow), it binds to it and, as a consequence, is transported into the cell in a vesicle.
*That's how viruses, and (mercury)
"Thiomersal" breaks down the cells.
When it comes into contact with a host cell, a virus can insert its genetic material into its host, literally taking over the host's functions. An infected cell produces more viral protein and genetic material instead of its usual products. Some viruses may remain dormant inside host cells for long periods, causing no obvious change in their host cells (a stage known as the lysogenic phase). But when a dormant virus is stimulated, it enters the lytic phase: new viruses are formed, self-assemble, and burst out of the host cell, killing the cell and going on to infect other cells. The diagram below at right shows a virus that attacks bacteria, known as the lambda bacteriophage, which measures roughly 200 nanometers.
Figure 5. Bacteriophage binding to and injecting their DNA into a bacterial cell.
As a doctor explained, “If the colored population becomes aware that accepting free hospital care means a post-mortem, every darky will leave Macon County...” Even the Surgeon General of the United States participated in enticing the men to remain in the experiment, sending them certificates of appreciation after 25 years in the study. Even when penicillin —the first real cure for syphilis— was discovered in the 1940s, the Tuskegee men were deliberately denied the medication.
Dr. J.W. Williams, who was serving his intership at Adrews Hospital at the Tuskegee Ins. in 1932 and assisted in the experiment's clinical work, stated that "neither the interns nor the subjects knew what the study involved." "The people who came in were not told what was being done," Dr. Williams said, " We told them we wanted to test them. They were not told, so far as I know, what they were being treated for or what they were not being treated for." As far as he could tell, the subjects "thought they were being treated for rheumatism or bad stomachs." He did recall administering to the men what he thought were drugs to combat syphilis, and yet he thought back the matter, Dr. Williams conjectured that " some may have been a placebo." He was absoluetly certain of one point: "We didn't tell them we were looking for syphilis. I don't think they would have known what that was." (Jones p.5)
Charles Pollard recalls saying recieving a free examination and being told he had "bad blood" and that the physicians never mentioned syphilis to me, not even once. He thought he had been recieving treatment for "bad blood" since the first meeting. "They been doctoring me off and on ever since then, and they gave me blood tonic. (*At this time in the early 1930's treatment consisted of mercury (*thiomersal) and two arsenic compounds called arsphenamine and neoarsphenamine, known aslo by their generic name, salvarsan). (Jones pg. 5/6)
Thiomersal is very toxic by inhalation *(as seen from above), ingestion, and in contact with skin (* injections) (EC hazard symbol T+), with a danger of cumulative effects. When applied to human nerve cells it changes cell membrane permeability and induces programmed cell death. In the body, it is metabolized or degraded to ethylmercury (C2H5Hg+) and thiosalicylate.
Transferrin is also associated with the innate immune system. Transferrin is found in the mucosa and binds iron, thus creating an environment low in free iron, where few bacteria are able to survive.
* (sic) That's only if your not introducing a live, attenuated virus, which also contains mercury.
The mucous membranes (or mucosae; singular mucosa) are linings of mostly endodermal origin, covered in epithelium, which are involved in absorption and secretion. It is at several places continuous with skin: at the nostrils, the lips, the ears, the genital area, and the anus.
Transferrin imbalance can have serious health effects for those with low or high serum transferrin levels. A patient with an increased serum transferrin level often suffers fromiron deficiencyanemia.
A patient with decreased plasma transferrin can suffer from iron overload diseases and protein malnutrition. An absence of transferrin in the body creates a rare genetic disorder known as atransferrinemia; a condition characterized by anemia and hemosiderosis in the heart and liver that leads to many complications including heart failure.
Flu Mist Nasal Spray H1N1 Vaccine
The swine flu nasal spray formulation is a live, attenuated form of the virus that is sprayed into the nose. "Attenuated" means "weakened." The nasal spray does contain thimerosal *mercury. People who should not get the flu mist vaccine include:
But if mercury didn't work during Tuskegee, how is going to work now?
- Pregnant women
- Children under two years old
- People with asthma
- People with a compromised immune system
From: A. True Ott, PhD, ND
V.I.C. (Vaccine Injury Coalition)
1260 S. 1200 W. #3
Ogden, UT 84404
Contact Phone Number: 801-392-1635
Today, October 6, 2009, the Weber/Morgan Health Department began dispensing 'H1N1' "Swine Flu" nasal "flu-mist" vaccines to the general public, with the public announcement that all county "health departments" in the State of Utah would soon follow.
These vaccines are said to be "free" to the public - which is a false statement. The manufacturer of the "vaccine" - MedImmune Inc., has been paid handsomely for this serum by the federal government - thus the "vaccine" is not free at all. It has been paid for by our tax dollars. With the federal government, there is no such thing as a truly "free" benefit!
The news media has been blindly promoting this vaccine without mentioning the following risks:
1. The vaccine is composed of "live" viruses. The vaccine circular, page 21, section 17.2 warns under the heading "Vaccination with a Live Virus Vaccine": "Vaccine recipients or their parents/guardians should be informed by the health care provider that Influenza A (H1N1) 2009 Monovalent Vaccine Live, Intranasal is an attenuated live virus vaccine AND HAS THE POTENTIAL FOR TRANSMISSION TO IMMUNOCOMPROMISED HOUSEHOLD CONTACTS". (Emphasis added). In layman's terms, the "live viruses" can be "shed" and cause other people to become infected.
2. The virus included in the FluMist vaccine is NOT a naturally-occurring virus, but is a laboratory-created "Influenza Hemagglutinin and Neuraminidase VARIANT" that is protected by MedImmune U.S. Patent # 2008/0069821 A1.
3. According to the vaccine circular, this "live-virus" vaccine has not been tested, and is clearly experimental. The FDA has allowed it to be licensed solely under new "emergency" licensing provisions.
4. The vaccine dose contains 0.188 mg. of monosodium glutamate - a well-known brain excito-toxic compound. Placing this amount of MSG directly into the nasal passages can cause neurological adverse reactions.
I personally believe that providing this "live virus" spray to citizens will actually CAUSE the feared pandemic to occur. Based on the summer's events in the Southern Hemisphere, the W.H.O.'s "pandemic" has disappeared. The projected "2nd wave" in Australia and South America did not materialize. Therefore, there is no further justification for "pandemic level 6" status - and thus, no need for H1N1 live-virus vaccines to be given away "free".
Adsorption or DOCKING with the host receptor protein.
Entry or PENETRATION of the viral nucleic acid into the host cytoplasm.
BIOSYNTHESIS of the viral components.
Assembly (MATURATION) of the viral components into complete viral units.
RELEASE of the completed virus from the host cell.
Peace be upon you
Thiomersal - Wikipedia, the free encyclopedia
Read more: Types of H1N1 Influenza Vaccines: Live Virus Nasal Spray or Inactivated Virus Flu Shot | Suite101.com
Atransferrinemia - Wikipedia, the free encyclopedia
INTRODUCTION TO VIRUSES
Bad Blood: The Tuskegee Syphilis Experiment, Revised Edition (Paperback)
Peace be upon you