Today’s PIC 10/2/14

Ebola-RCourtesy of Dees Illustrations

EBOLA UPDATE from Jim Stone

ebolaDuring the course of practically any viral infection, vitamin C needs to go WAY UP, and in the case of Ebola, they go SKY HIGH. So high that all conventional wisdom with regard to vitamin C is irrelevant. The dosings I have below are absolute minimums. Remember, that for as long as Ebola is not in your area, do not waste your vitamin C supply by taking more than a tablet per day. If it comes to your area, as a precaution, take 4 or 5 grams per day until you get symptoms, THEN proceed with taking more. This is to preserve your supply until it is really needed

Here are the dosings:

These dosings are based upon extended observation of a puppy with parvo, and how much vitamin C was needed to stop the bleeding in a puppy that had the doggy version of Ebola, (I know, Parvovirus is not even close to being the same structurally but it does the same thing – causes a 90 percent mortality rate in untreated puppies over the course of 3 or 4 days, with death caused by massive hemorrhaging.) It is a hemorrhagic virus. I know there will be a few prudes out there who will say this is meaningless in relation to Ebola, OK, I heard you. Do nothing and die then.

If I dosed the puppy with 125 mg/KG daily of ascorbic acid, there was reduced but still noticeable internal bleeding. If I dosed the puppy with 125 mg/KG ROSE HIP vitamin C daily, it stopped all bleeding. So rose hip vitamin C works better. But if I dosed the puppy with 175 mg/KG daily of ascorbic acid, this also stopped all bleeding, so ascorbic acid is cheaper at that rate. If I discontinued dosing, life threatening bleeding occurred (and obviously the puppy rapidly got a 175mg/KG dose, which again would immediately stop all bleeding.) It was like vitamin C flipped a switch between life and death for that puppy. Now, two weeks into this (a long time for parvo) I can skip dosing and nothing serious happens. During the entire time, as long as the puppy got it’s vitamin C it ate and drank normally, and had only slight symptoms of being a little bit sick. Prior to trying vitamin C, (at the end of day two of the bleeding early on) the puppy was seriously dehydrated and close to death. Vitamin C caused a rapid reversal of this condition.

Vets will say this has to be bogus, because dogs make their own vitamin C. My response? YES, at a rate of 18 mg/KG daily, far below what is needed when a serious illness sets in.

So, now we have two things – a practically assured way to keep any puppy from dying of parvo (a breakthrough by itself), and a possible minimum reference for vitamin C dosing for Ebola.

ABSOLUTE MINIMUM DOSING: 200 mg/KG (91 mg/pound) for people. This means that if you weigh 10 pounds, you need a gram a day. If you weigh 100 pounds, you need 8.2 grams per day. A 50 KG woman will need 10 grams. And these are minimums, it will not hurt at all to go much much higher with the dosings.

I experimented with that puppy to find out right where the threshold was. It is 175 (shot down it’s throat) plus 18 milligrams/KG the dog naturally produced by itself daily so to keep it all simple just go with 200 mg/kg.

How vitamin C works to stop the damage from Ebola (though vitamin C is NOT a cure)

First of all, as anyone who knows about scurvy can state, vitamin C helps blood vessel walls keep their strength. But there is something far more serious at play with Ebola that vitamin C impedes. Something even more sinister than blood vessel weakening happens when Ebola depletes ALL vitamin C, and that is a greatly accelerated release of blood vessel damaging cytokine IL-6. Any medical professional will be able to quickly look up the fact that vitamin C impedes the release of cytokine IL-6, which Ebola causes severe releases of in blood vessel walls. Once released in huge amounts, IL-6 further irritates blood vessel walls to such an extent it can blow holes in them, and this, combined with the already weakened condition from a lack of vitamin C will cause many vessels to rupture.

In short, vitamin C is like a magic Ebola bullet that not only curtails the release of blood vessel damaging cytokine IL-6, it also, at the same time, makes blood vessels return at least to normal strength (and possibly beyond with very high dosings.) These two things working together make vitamin C the probable best first line of defense against Ebola that is possible.

But there is more to this story than that…

Since IL-6 plays a huge role in damaging blood vessels, it is important to stop its release. And there are some very simple foods that can be eaten that facilitate this. The first is green tea. Green tea can curtail cytokine IL-6 release by 21 percent (which pales compared to vitamin C, but would be a bonus). Of similar value are apples, cinnamon, most berries, choke cherries, pomegranates, olive oil, flax seed oil and fish oil.

You should avoid caffeine and chocolate, because though both have the potential to help in some ways, they also have the potential to totally offset all benefit in everything else eaten (but this has not been fully studied out by anyone with regard to Ebola as far as I know of,) it is just that doctors who know this a whole lot better than I do say the chemistry could possibly go very negatively, so to be safe, avoid caffeine and chocolate.

The foods mentioned above pretty much round out the list as far as I know, and further playing around with things like garlic (which is great for practically anything) and hot peppers, ginseng and other blood thinning foods will probably be detrimental with a hemorrhagic fever.

The bottom line is that if Ebola does take off, those in the know do not just have to sit in fear and wait for death to come. Diet and vitamin C can easily make the difference between practically living normally through it all, or dying.

AND A VERY IMPORTANT NOTE: Unscrupulous scammers are EVERYWHERE who will try to sell you this that and hay from an old barn as an Ebola cure, there is a lot of evil out there and I strongly suggest you avoid ALL OF IT, what is here is probably #1 above and beyond any other hope (and I cannot profit from this at all.)

Additionally, it is VERY IMPORTANT to note that the doctor who gave me the lead on Vitamin C and Ebola has told me repeatedly that my recommended dosings above are too low, so make sure you have a LOT of vitamin C laying around just in case you need to go far beyond what I have recommended here, and as I have always said, keep your current dosing down to no more than 1 tablet per day at this time, until there is a very good reason to start taking large amounts of vitamin C (to avoid wasting it).

There have been a few doctors out there who have hopped on this issue, to smash the word that Vitamin C actually may work to prevent death from Ebola. To them I have to say, PROVE ME WRONG. I may not be a doctor, but I am also not medically illiterate and know legitimate work when I see it, and the above came directly from other doctors who were intrigued, and said THE CHEMISTRY SURE FITS.

To the thinking crowd: Is $20 too much to spend on a large amount of cheap vitamin C purchased in advance as a just in case? So what if for some obscure reason no one calculated it ends up not working, WHAT DID IT COST YOU? Remember, the same doctors who will speak out against this will load your baby up with Thimerosal or a brain eating vaccine administered genetically engineered phage just because the package said to do it, what do they really know anyway?

The following report, from honest doctors, helps bulldoze the liars and adds a LOT of detail.

I came up with the above independent of the following report (and therefore what I say above varies slightly but is pretty much the same.) The following report adds a ton of detail to what I said above. If you can handle a long read, what they say here is EXCELLENT. I have linked the following report simply because it is obviously accurate, and gets into the tiny details I cannot write in with the limited time I have. I thank these honest doctors for laying out the details so nicely.

Commentary by Steve Hickey PhD, Hilary Roberts PhD, and Damien Downing MBBS, MSB.

(OMNS Aug 20, 2014)

If there were a drug that worked on Ebola you should use it. There isn’t. There is only vitamin C. But you must be extremely careful what you believe, because, as it ever was, the Internet is full of dangerous loonies. For coming up to a decade now the OMNS has reported on nutritional therapies; we leave the medical politics to one side and work from the facts. Here are the facts about vitamin C and Ebola.

1. Taking a gram or so of day of vitamin C won’t protect you against anything except acute scurvy; it doesn’t matter whether the vitamin is liposomal, nano-particles, or even gold-plated. Beware of websites, companies, and Youtube clips making wild and unsubstantiated claims about the efficacy of vitamin C.

2. Clinical reports suggest that taking vitamin C almost to bowel tolerance every day (in divided doses) will help to protect you against all viruses. Reports by independent physicians have been consistent for decades. However, the doctors also stipulated most emphatically that the dose and the way you take it must be right – or it will not work. There is no direct placebo controlled “evidence” that massive doses of vitamin C will work on Ebola, and nobody would volunteer to take part in that study. But massive doses are reported to have helped against every virus it has been pitched against. This includes Polio, Dengue and AIDS, and it even makes vaccination work better. In the 1980s when no other treatment was available it was reported that full blown AIDS could be reversed and the patient brought back to reasonable health.[i,ii]

At risk or worried about Ebola? This is what you should do.

Vitamin C

Vitamin C is the primary antioxidant in the diet. Most people do not take enough to be healthy. While this is true of many nutrients, vitamin C is a special case. Ignore governments telling you that you only need about 100 mg a day and can get this amount from food. The required amount of vitamin C varies your state of health. A normal adult in perfect health may need only a small intake, say 500 mg per day, but more is needed when someone is even slightly under the weather. Similarly, to prevent illness, the intake needs to be increased.

The intake for an otherwise healthy person to have a reasonable chance of avoiding a common cold is in the region of 8-10 grams (8,000-10,000 mg) a day. This is about ten times what corporate medicine has tested in their trials on vitamin C and the common cold. Ten grams (10,000 mg) is the minimum pharmacological intake; it may help if you have a slight sore throat but more (much more) may be needed. To get rid of a common cold, you may need anything from 20 to 60 grams (60,000 mg) a day. With influenza the need might be for 100 grams (100,000 mg) a day. Since it varies from person to person, and from illness to illness, the only way to find out is to experiment for yourself.

Dynamic flow

The problem with oral intakes is that healthy people do not absorb vitamin C well due to something Dr Robert Cathcart called bowel tolerance. [iii] Take too much of the vitamin in a single dose and it will cause loose stools. In good health, a person might be able to take a couple of grams at a time without this problem. Strangely, when a person becomes sick they can take far more without this side effect: as much as 20-100+ grams a day, in divided doses. [iv]

High dose vitamin C has a short half-life in the body. The half-life is the time for the level in the blood plasma to fall back to half its concentration. Until recently, some people claimed that the half-life of vitamin C was several weeks. We have shown that this long half-life applies only to very low doses.[v] By contrast, the half-life for high blood levels is only half an hour. This short half-life means that for high dose vitamin C the period between doses needs to be short – a few hours at most.

The aim is to achieve dynamic flow, to get vitamin C flowing continuously through the body. Dynamic flow requires multiple high doses taken throughout the day. When separated in time, each dose is absorbed independently. Two doses of 3 grams, taken 12 hours apart, are absorbed better than 6 grams taken all at once. Multiple large doses, say 3 grams four times a day, produce a steady flow of the vitamin from the gut, into the bloodstream and out, via the urine. Some of the intake is not absorbed into the blood and stays in the gut, as a reserve against the early onset of illness. As illness begins, the body pulls in this “excess” to help fight the virus.

The idea behind dynamic flow is that the body is kept in a reduced (antioxidant) state, using high doses. There is always vitamin C available, to refresh the body and other antioxidants. Each vitamin C molecule (ascorbic acid) has two antioxidant electrons, which it can donate to protect the body. It then becomes oxidised to dehydroascorbate (DHA). This oxidized molecule is then excreted, so the body has gained two antioxidant electrons. The kidneys reabsorb vitamin C, but not DHA; the vitamin C molecule is absorbed, used up, and then the oxidized form is thrown out with the rubbish.

The effectiveness of vitamin C is not directly proportional to the dose; it is non-linear. There is a threshold above which vitamin C becomes highly effective. Below this level, the effect is small; above it, the effect is dramatic. The problem is that no-one can tell you in advance what intake of vitamin C you need. The solution is to take more – more than you think necessary, more than you consider reasonable. The mantra is dose, dose, dose.

Types of Vitamin C

Straightforward, low cost ascorbic acid is the preferred form of supplement. Vendors may try to sell you “better absorbed” forms with minerals or salts such as sodium, potassium or calcium ascorbate, and so on. These are irrelevant, if not counterproductive, for high intakes.

It is worth noting the following:

Timing is more important than form. Two large doses of ascorbic acid taken a little time apart are better absorbed than a single dose of mineral ascorbate.

Mineral ascorbates are salts and do not carry the same number of antioxidant electrons. Ascorbic acid has two electrons to donate while a salt typically has only one. With high doses, the “improved” forms are thus only about half as effective. This is consistent with reports that mineral forms are correspondingly ineffective in combating illness.

Ascorbic acid is a weak acid, much weaker than the hydrochloric acid in the stomach. Mineral ascorbates may be better tolerated, as they make the stomach more alkaline than ascorbic acid. However, an alkaline stomach is not a good idea – there are reasons the body secretes hydrochloric acid into the stomach, including preventing infection. Furthermore, if you are coming down with a hemorrhagic viral infection, mild discomfort will not be something of great concern.

For high intakes, capsules of ascorbic acid are preferable to tablets. This is because tablets are packed with fillers and it is not wise to take massive doses of these chemicals. Check the ingredients – you want to take ascorbic acid and very little else. Bioflavonoids are alright, and the capsules may be made with gelatine or a vegetarian equivalent.

The cheapest way to take ascorbic acid is as powder, dissolved in water. If you do this, use a straw to avoid it getting on the tooth enamel, as it is slightly acidic. You will need a set of accurate electronic scales to monitor the dose. If you do not weigh it carefully, it will be difficult to keep close to bowel tolerance.

Intravenous Vitamin C

Ideally, infected people would be given a continuous intravenous (IV) infusion of massive doses of vitamin C (sodium ascorbate is preferred as ascorbic acid is irritant to veins).

People who are sufficiently ill will not be able to take vitamin C by mouth.
IV provides the highest possible blood levels
IV means continuous drip, not an injection (short half-life)
Unless you are a medical professional who can treat yourself and your family, or are exceptionally rich, IV ascorbate will not be an option in an Ebola outbreak. (Admin insert – and therefore stocking up on cheap ascorbic acid in tablet or powder form will be the thing to do.)

Rectal Vitamin C

Rectal administration of sodium ascorbate is a method that can be used in emergencies, and in developing world circumstances, when IV is unavailable or unsuitable. Nurses can quickly be trained to mix 15-30 g of sodium ascorbate in 250-500 ml clean water, and give it by enema. It can be safely and effectively used in children. An enema also removes from the bowel material that may be challenging. This has been done successfully with aboriginal people in the Australian outback.

Liposomes

In healthy people, liposomes help the absorption of oral vitamin C; in some circumstances this is also true for sick people. However, we need to dispel some popular myths.

In a healthy person, higher blood levels (about 600 microM/L) can be achieved using liposomal vitamin C compared with standard ascorbic acid (about 250 microM/L). We were the first to demonstrate this fact experimentally.[vi] However, the two absorption methods are different and if both are used together the resultant plasma levels are additive (something like 600 + 250 = 850 microM/L). Since ascorbic acid is much cheaper than liposomal vitamin C, it is cost effective for a healthy person to start with ascorbic acid and top up with liposomes as required.

When a person becomes ill they can absorb massive doses of standard ascorbic acid, using the dynamic flow approach. So if you are sick, taking a gram of liposomal vitamin C instead of a gram of cheap ascorbic acid will provide little extra benefit. Both will be well absorbed , and the liposome contains sodium ascorbate which is less effective. Liposomes only provide added benefit once the sick person has approached bowel tolerance levels, using standard ascorbic acid.

Liposomal vitamin C is NOT more effective than IV for fighting acute infections. This suggestion is unscientific and unsupported by data. We prefer liposomes for chronic infections and cancer, but this does not extend to acute illness. There is also a lot of hype around the fact that liposomes can be absorbed directly into cells. Many liposomes are absorbed from the gut and pass into the liver, where they are stored and the vitamin C released. Liposomes may also float around in the bloodstream, lymph nodes, and so on, waiting to release their contents or be taken up by cells. But the cells that take up the liposomes are not necessarily those that are most in need of vitamin C. Moreover cells may suffer side effects; liposomes are basically nanotechnology and have additional theoretical issues.

Prevention

To have a reasonable chance of avoiding a major viral infection, a daily intake of at least 10 grams of ascorbic acid is needed. The idea is to start low, taking say 500 -1,000 mg four times a day. Build up the intake to close to bowel tolerance; increased wind and large soft stools will occur before diarrhea signals that bowel tolerance has been exceeded. At this stage, back off the dose a little, to a reasonably comfortable level.

Admin insert – this goes along with my initial advice – take ONE tablet per day until Ebola is in your area, when Ebola arrives increase this to 4 or 5 grams per day. If you stop having soft stools from over doing it, it means you have a virus (because your body will start taking in the vitamin C) so THEN start taking large amounts. 

At the first hint of an infection – feeling unwell, itchy throat, fatigue, and so on – take more ascorbic acid. If the hint of impending sickness is mild, take perhaps 5 grams every half hour or even more frequently. Anything more than a hint of infection, take as large a dose as you feel could be tolerated and follow this by taking 5 grams every half hour. The rule is to take as much as you can without going over the tolerated level: you will probably be taking too little, even though you are trying hard to take a massive dose.

If you are already in dynamic flow and want extra protection, then add liposomal vitamin C. Take it at the same intervals as the ascorbic acid; that is several times a day. The limit is once again bowel tolerance – take too much and it will give you loose stools. This will provide the maximum preventive effect, for the lowest cost.

Admin insert – LOOSE STOOLS ARE THE KEY. If you are not getting diarrhea it means you need MORE VITAMIN C. If you are getting diarrhea, CUT BACK because you are wasting it.

Treatment

We assume that you are not a medical professional and do not have access to IV ascorbate. However, if IV sodium ascorbate is available, it should be given slowly and as continuously as possible. For children, enemas may be the most practical method (we hope to publish practical instructions for this soon). Medical professionals can deal with such things with little difficulty, but others may do more harm than good.

The first important thing is to start the treatment early. The longer a person waits after the initial symptoms, the less effective the treatment will be. Also if the illness is allowed to develop the sick person may become unable to take anything orally.

Once again, the idea is to get dynamic flow going with as much ascorbic acid as can be tolerated. In this case, the doses are massive. Five to ten grams every half hour, through the day, will provide 120 to 240 grams a day. Even at this high intake, the blood plasma levels may be low or undetectable; at most 250 microM/L will be achieved. So the question then becomes how much additional liposomal vitamin C the patient can tolerate.

A practical approach would be to start with 5 grams of ascorbic acid and a similar amount of liposomal vitamin C in very frequent doses. Remember the key is dose, dose, dose. More vitamin C!

How it Works

The mechanism of action of high dose vitamin C is known and understood. In normal healthy tissues it acts as an antioxidant. In other tissues, it generates hydrogen peroxide, the chemical that platinum blondes use to bleach their hair. This happens in sick and inflamed tissues, for example in a malignant tumor. The process is typically a form of Fenton reaction, generating free radicals. The oxidation and free radicals arising from the hydrogen peroxide kill bacteria and inactivate viruses. In other words, vitamin C acts as a targeted bleach and antiseptic.

Admin insert – IL-6 Cytokine inhibition via vitamin C with regard to Ebola is Ebola specific, and something these doctors do not know about. But that is largely irrelevant since they at least clearly state here that vitamin C is the key

Vitamin C is unique, because it has low toxicity and can be taken safely in massive amounts. Other antioxidants and supplements will not have a similar effect. Do not be confused and think that Echinacea, for example, will help. Yes, there may be supplements and herbs that provide a little immune system support, but this is Ebola we are talking about – get real!

Note, vitamin C is not some magical antitoxin; this idea is a metaphor. A disease such as Ebola is not caused by toxins that are inactivated by vitamin C. Free radicals are not toxins. Oxidants are not toxins. Vitamin C nearly always acts by transferring electrons, as an oxidant or antioxidant. It is just basic chemistry. Also, it does not matter if you have poor dental hygiene, this will hardly affect how massive intakes of vitamin C tackle an acute viral infection.

Interactions Sugar interferes with the uptake of vitamin C. If you are using vitamin C to combat a viral infection do not eat any sugar or carbohydrates (long chain sugars) or the vitamin C will not be absorbed properly. We stress that this means no sugar and no carbs, at all.

Smoking releases enormous amounts of oxidants and free radicals into the bloodstream. The vitamin C will expend itself, trying to mop up the chemicals from the smoking. We have no moral objections to people smoking: it is a personal choice. However, smoking will hinder even massive doses of vitamin C from preventing infection. Once infected with Ebola, smoking will stop the vitamin C from keeping you alive.

It is sensible also to supplement with a little chelated magnesium, such as magnesium citrate, which helps overcome the (largely theoretical) risk of kidney stones.

The reaction that generates hydrogen peroxide in sick tissues can be enhanced a little by taking selenium with the vitamin C. A little caution is needed as too much selenium will cause diarrhea, fatigue, garlic breath, and hair and nail loss; severe toxicity can have more severe effects but is hard to achieve. Methylselenocysteine is a less toxic form and this would be our choice. The normal intake is perhaps 100-200 micrograms (0.1-0.2 mg) a day; we would take 400 micrograms a day during an epidemic and up this to 1,000 micrograms (one milligram) a day, at the initial onset of symptoms. It is possible to go up to 3 mg for short periods, with medical supervision.

Other supplements may be synergistic with vitamin C. Alpha-lipoic acid can be taken at reasonably high levels reasonably safely. We would take up to a gram or two a day (1,000-2,000 mg) in the short term. Vitamin K also helps with blood clotting and is safe in the recommended amounts – we would get the highest dose vitamin K2 supplement available. Note vitamin K is contraindicated in those with clotting disease or those on blood thinners such as warfarin.

Contraindications

The only established side effects of ascorbate therapy are wind, loose bowels and chronic good health. There are some contraindications; people with kidney disease, iron overload disease, or glucose-6-phosphatase deficiency should not immediately take high doses of vitamin C. In the setting of an epidemic they can start as we recommend but should increase more cautiously, with appropriate medical monitoring.

Why Put This Out?

People need to know that vitamin C is an option for fighting Ebola, and how it works. There is a great deal of misinformation, particularly on the internet, both from vested interests and from “loonies”. Moreover, in an Ebola epidemic vitamin C supplements may be hard to source.

This account is intended for intelligent adults, who can make their own rational decisions and take responsibility for their health. We strongly promote the idea that medicine should be based on rational patients, rather than authoritarian doctors. Doctors are there to provide the information for patients, to help them choose between available options. This is information only – what you decide to do with it is up to you.

In our opinion the use of vitamin C in Ebola is a no-brainer. Get the illness and, it is said, you have at best a 50-50 chance of surviving without vitamin C-based therapy. Corporate medicine has no effective treatment. Furthermore, if a drug were available, it would be untested and almost certainly unavailable to you, dear reader. Vitamin C is considered safe and should do no harm. The cost of treatment is low. The clinical reports of vitamin C in viral infection are that if you get the dose right, you will survive. Vitamin C is known experimentally to inactivate viruses. In the event, we hope people make rational decisions.

If you hate this web site (but hit it anyway because you have a web site and get tips from here like Gordon Duff) and you do not want to link this site, AT LEAST link to the report by these doctors, it is so close to what I said anyway that it can be considered at least as good.

Related:

Complete confirmation Vitamin C recommendation for ebola is not sabotage

Today I got final confirmation that washes with my medical knowledge, here goes:

The actual way ebola kills is by causing a severe cytokine release in blood vessel walls, which if already irritated by a viral assault, will rupture from the irritation caused by a strong cytokine release. With regard to ebola, the exact cytokine is called IL-6, which is inhibited by 41 percent with adequate vitamin C present. This means, that from this mode of action alone, vitamin C will reduce the impact of ebola by 41 percent. If you combine this with the fact that vitamin C will strengthen the blood vessel walls as well, the two ways vitamin C helps will work in combination to prevent death from ebola, especially if ebola, which removes all vitamin C weakens the blood vessel walls by removing vitamin C to begin with. But there is more to this than that, diet can play a huge role and this will be tomorrow’s main report, I am still digging and pulling stuff together.

The bottom line is that it really appears ebola can be beaten just by eating the correct foods and getting enough vitamin C (and absent correct foods, vitamin C is pretty much a magic bullet) but diet can also help a LOT.

Source: http://jimstonefreelance.com/finalebolavitc.html

BREAKING NEWS: Anonymous Doctor Releases Treatment for the Ebola Virus

breakingnewstarapour20101209014526233The treatment for Ebola, along with accompanying MOA (Method Of Action) has been sent to this web site.

Jim Stone, August 1, 2014
Permalink

This is a lengthy article, DO NOT SURFACE READ. The actual treatment for ebola which will virtually eliminate fatalities, as revealed by a doctor who has worked with ebola, is below.

Consider this: The elite would never release a plague without an easy cure, and along with this ebola outbreak an American biowarfare firm has been working in Sierra Leon for the last five years. Google that. Sierra Leon has actually identified them as the perpetrators of this outbreak and kicked them out of the country. There is absolutely no doubt this outbreak was intentionally caused by the U.S. war department.

And if it is intentional, a cure is known. There would simply be no other way to do business.

Here is the treatment, complete with MOA. This is a treatment and not a cure, your immune system wipes out the virus, and the treatment gives your immune system time to do it. Here is what Ebola does that is fatal: It causes the complete removal of all vitamin C from the body. No one actually knows what mechanism is involved in doing this, other than a malfunction that is not permanently destructive to whatever is triggered to remove all vitamin C. All the researchers know is that vitamin C drops to zero and all the symptoms of ebola are consistent with a complete loss of vitamin C.

How do I know this? A doctor who has remained anonymous and has worked with ebola victims has discovered this and sent it to this web site, at last check this cannot be googled which confirms this doctor did not just copy paste, SO POST IT EVERYWHERE; GET THIS OUT THERE, THE TREATMENT FOR EBOLA WHICH WILL PREVENT DEATH IS KNOWN AND THIS IS AN EMERGENCY REQUEST FOR MY READERS TO SPREAD THIS INFO AND STOP THIS EBOLA ATTACK IN ITS TRACKS.

From an anonymous doctor:

Summary:

“The very first symptoms of ebola are exactly the same as scurvy, which is caused by inadequate vitamin C. Though scurvy is seldom fatal as a primary condition, scurvy also represents only a partial deficiency of vitamin C, the body still has a LOT of vitamin C compared to zero, which ebola causes. Absent ANY vitamin C, blood vessels become very weak and start to lose blood, and platelets become ineffective and unable to trigger clots. So death by ebola is caused by massive internal bleeding and loss of blood, which can be stopped simply by taking enormous doses of vitamin C until the immune system succeeds in killing off the virus.”

Begin text:

Ebola is probably the best known of a class of viruses known as hemorrhagic fever viruses. In fact, Ebola virus was initially recognized in 1976. Other less known but related viral syndromes include yellow fever, dengue hemorrhagic fever, Rift Valley fever, Crimean-Congo hemorrhagic fever, Kyasanur Forest disease, Omsk hemorrhagic fever, hemorrhagic fever with renal syndrome, Hantavirus pulmonary syndrome, Venezuelan hemorrhagic fever, Brazilian hemorrhagic fever, Argentine hemorrhagic fever, Bolivian hemorrhagic fever, and Lassa fever. The Ebola virus infection, also known as African hemorrhagic fever, has the distinction of having the highest case-fatality rate of the viral infections noted above, ranging from 53% to 88%.

These viral hemorrhagic fever syndromes share certain clinical features. The Cecil Textbook of Medicine notes that these diseases are characterized by capillary fragility, which translates to easy bleeding, that can frequently lead to severe shock and death. These diseases also tend to consume and/or destroy the platelets, which play an integral role in blood clotting. The clinical presentation of these viral diseases is similar to scurvy, which is also characterized by capillary fragility and a tendency to bleed easily. Characteristic skin lesions develop, which are actually multiple tiny areas of bleeding into the skin that surround the hair follicles. some cases even include bleeding into already healed scars.

In the classic form of scurvy that evolves very slowly from the gradual depletion of vitamin C body stores, the immune system will be sufficiently compromised for infection to claim the patient’s life before the extensive hemorrhage that occurs after all vitamin C stores have been completely exhausted. Ebola virus and the other viral hemorrhagic fevers are much more likely to cause hemorrhaging before any other fatal infection has a chance to become established. This is because the virus so rapidly and totally metabolizes and consumes all available vitamin C in the bodies of the victims that an advanced stage of scurvy is literally produced after only a few days of the disease.

The scurvy is so complete that the blood vessels generally cannot keep from hemorrhaging long enough to allow an infective complication to develop. Also, the viral hemorrhagic fevers typically only take hold and reach epidemic proportions in those populations that would already be expected to have low body stores of vitamin C, such as is found in many of the severely malnourished Africans. In such individuals, an infecting hemorrhagic virus will often wipe out any remaining vitamin C stores before the immune systems can get the upper hand and initiate recovery. When the vitamin C stores are rapidly depleted by large infecting doses of an aggressive virus, the immune system gets similarly depleted and compromised. However, this point is largely academic after hemorrhaging throughout the body has begun.

To date, no viral infection has been demonstrated to be resistant to the proper dosing of vitamin C as classically demonstrated by Klenner. However, not all viruses have been treated with Klenner-sized vitamin C doses, or at least the results have not been published. Ebola viral infection and the other acute viral hemorrhagic fevers appear to be diseases that fall into this category. Because of the seemingly exceptional ability of these viruses to rapidly deplete vitamin C stores, even larger doses of vitamin C would likely be required in order to effectively reverse and eventually cure infections caused by these viruses.

Cathcart (1981), who introduced the concept of bowel tolerance to vitamin C discussed earlier, hypothesized that Ebola and the other acute viral hemorrhagic fevers may well require 500,000 mg of vitamin C daily to reach bowel tolerance! Whether this estimate is accurate, it seems clear as evidenced by the scurvy-like clinical manifestations of these infections that vitamin C dosing must be vigorous and given in extremely high doses. If the disease seems to be winning, then even more vitamin C should be given until symptoms begin to lessen. Obviously, these are viral diseases that would absolutely require high doses of vitamin C intravenously as the initial therapy. The oral administration should begin simultaneously, but the intravenous route should not be abandoned until the clinical response is complete. Death occurs too quickly with the hemorrhagic fevers to be conservative when dosing the vitamin C. (from Vitamin C, Infectious Diseases, and Toxins:Curing the Incurable by Thomas E. Levy MD JD)

MY COMMENT: I may not be a doctor, but I am awful good with medical topics, and this rings 100 percent true, IT IS THE MOA which if combined with some of my medical knowledge, such as the fact that Broccoli is absolutely excellent for assisting the clotting of blood, that the active component of Noni (which is in pineapple juice) is strongly anti viral, and that cures such as colloidal silver, while good for bacterial infections does nothing for viruses, combine some real knowledge with what this doctor says and it is highly probable that Ebola can be shrugged off as a mild case of scurvy.

Beware the current Colloidal Silver psy op, the actual cure for Ebola has been given to this web site.

Colloidal silver is great stuff, and I have made gallons from a 1 ounce silver bar myself. It works great for curing BACTERIAL infections and making water safe to drink without the nasty taste of iodine. HOWEVER, COLLOIDAL SILVER WILL DO NOTHING AGAINST VIRUSES, AND HUGE LIES ARE BEING HATCHED RIGHT NOW TO MISGUIDE PEOPLE TO A FALSE EBOLA CURE AND THE ALTERNATIVE MEDIA IS LAPPING IT UP

All curative agents have a mode of action, or MOA. And if anyone posting medical cures does not know the MOA, they have no idea what they are talking about. Colloidal silver has an MOA that has been known for many decades, yet recently Google has been rigged to bury it with only articles stating “the MOA is being explored and we think it is ___(then disinfo)” and there has to be a reason why this is being done right now, at this point in time with Ebola running amok.

Here is how colloidal silver actually works (its MOA), with first an example: Colloidal silver is to bacteria what cyanide is for all red blooded organisms. In red blooded organisms, cyanide binds with hemoglobin in place of oxygen, and makes it impossible for blood to carry oxygen. With enough cyanide, oxygen starvation via cyanide bonded hemoglobin causes death.

Colloidal silver does the same for bacteria, it binds with the oxygen carriers in bacteria permanently, causing bacteria to quickly die from oxygen starvation. This is the MOA for colloidal silver, which has been clearly known practically forever.
VIRUSES HAVE NO METABOLIC PROCESSES WHICH REQUIRE AN OXYGEN CARRIER, AND THEREFORE COLLOIDAL SILVER WILL BE COMPLETELY INEFFECTIVE AGAINST EBOLA, do not let the misinformed in the alternative media fool you by saying colloidal silver is effective against viruses in any way, colloidal silver is only useful for treating secondary bacterial infections that move in after a preceeding viral infection and in the case of ebola, there is not enough time for that to make a difference.

It is extremely important to note that a HUGE psy op is underway to fake colloidal silver as a cure for viruses and there HAS TO BE A REASON, DO NOT FALL FOR IT.

WW~Notes: FORWARD THIS TO EVERYONE!!!!!!!!!!!!!!!!

The Ebola Outbreak: The “Pandemic” that isn’t.

WW~Notes: Thanks to B’Man’s comments we now have some real information on the Ebola psy-op scare.  I want to thank him for contributing his knowledge and skepticism to put us all at ease, especially me.  Below is the article from Removing the Shackles.

 

There have been many many moments over the past few years that have made me ponder my past and the experiences and knowledge that I have gathered along the way.  I cannot tell you how many times in the last two years alone that I have had major personal revelations about things that I have gone through or learned in the past that are suddenly so relevant in the NOW.  Last night was one of those moments.

For almost 20 years I have had an almost morbid fascination with the Ebola virus, and haemorrhagic fevers  such as Marlburg and Lassa, in general.  It started when I read the book “The Hot Zone” in 1996, and continued when I worked with a former US Special Forces Military doctor in Thailand who had a vast amount of knowledge on the Ebola virus.  Ever since then I have read possibly hundreds of medical reports and studies on the topic….  reports and studies that were written before this so called “outbreak” and the very blatant editing that has been perpetrated across the media.

….. obviously to prepare myself for this article today.

…. Very interesting that the Wikipedia listing for Ebola Zaire doesn’t specify how the virus is transmitted, don’t you think?

If you’ve read any main stream media news outlet or alternative news site, you’ve heard all the panicked fear mongering about the purported “Ebola” outbreak in west/central Africa.  These reports started appearing in the main stream media news in February 2014 while I was in Malta.  I immediately started following the news and kept abreast of the latest developments.  I also immediately started to smell a rat.  The Media banged on the fear porn drum for a few weeks and then it all just sorta disappeared (they couldn’t seem to keep people’s attention on “world war III” starting in the Ukraine AND the “pandemic of Ebola”  at the same time).   Then in the past few weeks they’ve ramped up the Ebola fear porn drama again…..

…. Distract Distract Distract.

Ukraine didn’t work out the way they wanted so they needed another distraction.  Enter the insanity of Netanyahu  and the debacle being played out in the Gaza strip.  But now that is not working out for them either as the world is standing up and shining the light of outrage on Gaza.  So another distraction is necessary.  Enter: Ebola panicked “pandemic” in africa.

I am not going to get into all the main stream media Ebola circus- open any news website and you can read it all- but I will discuss several glaring pieces of obvious bullshit, and “facts” that the so called medical professional associations have invented to perpetuate this travesty.

“Their” goal is only one thing: FEAR & DISTRACTION.   They need to keep the public distracted from the fact that their entire financial world empire has crumbled to the ground and they have lost everything they have. …. I’ll be going into details on this subject in my next article.   For this moment I will focus on the fear porn campaign that “they” are currently pushing onto the public.

Before I start posting the links and my commentary, I will post this note that I wrote in one of my Skype rooms as an intro to the topic:

 D.breakingthesilence:  “they’ve” been trying to weaponize ebola for over 40 years.  they can’t do it because the Mayinga strain of ebola (the only known strain to be contagious through aerosol transmission) kills people too quickly for it to work as a broad spread bio weapon.  they’ve been playing with the Marlburg/ebola crosses to create a virus with a longer gestational period so that cross infection/contamination will spread farther.  but Marlburg cancels out the aerosol transmission factors of the Mayinga strain of ebola, which leaves them with oral/mucous membrane transmission, which isn’t effective as the virus dies very quickly unless it’s in a very hot humid climate (hence the fact that they do their testing in western Africa in jungle climates).  Air conditioning kills the virus almost instantly.”

The first article I will post here is to show the vast amount of disinfo that is being spread by official “government” agencies about the Ebola virus.  This article by Mike from Natural News shows the dangers of assuming that these “official” agencies are telling the truth.  (Which I find strange as I know that Mike is usually not fooled by these type of things).


 

Ebola transmission by aerosols confirmed: virus survives for days outside infected hosts

Learn more: http://www.naturalnews.com/046276_Ebola_aerosol_transmission_infectious_disease.html#ixzz39FOxeNiE
|
(NaturalNews) Today Kurt Nimmo from Infowars.com is incorrectly reporting that “aerosol transmission is not possible” with Ebola. (2) That statement is part of an article entitled, “Don’t Fear Ebola, Fear the State” which is, overall, a very compelling article.

Nimmo is a fantastic writer and a great researcher, but in this case his statement is factually incorrect and probably needs to be addressed. As clearly explained by the Public Health Agency of Canada: (3)

“INFECTIOUS DOSE: 1 – 10 aerosolized organisms are sufficient to cause infection in humans.”

Ebola, you see, can “ride” on aerosolized particles of blood, mucous and other body fluids. Someone sneezing, for example, can cause Ebola viruses to be aerosolized where they land on other people’s hands or faces. It only takes one virus entering the corner of your eye (or the corner of your mouth) to set off a full-blown infection……\

…..Even worse, Ebola is a strong survivor outside a host. Here’s what the Public Health Agency of Canada says:

SURVIVAL OUTSIDE HOST: The virus can survive in liquid or dried material for a number of days. Infectivity is found to be stable at room temperature or at 4 C for several days, and indefinitely stable at -70 C. Infectivity can be preserved by lyophilisation.

http://www.naturalnews.com/046276_Ebola_aerosol_transmission_infectious_disease.html#ixzz39FPV3ASc


 

Both of these statements by the Canadian “government” are incorrect and appallingly shine a light on the fact that the real FACTS about Ebola is being covered up, changed and re-written.

Let me give you some hard core facts about Ebola:

Ebola has only ONE strain that is suspected to of been transmitted by aerosol exposure to the live virus.  This is an absolute FACT.   The Ebola Zaire strain called “Mayinga”, named after the nurse, Mayinga, who died after being infected with the virus without any known method of transmission meaning that they suspect that she died through an aerosol transmission (as in: micro particles that are actually in the air, and transmitted through contact with the virus ONLY by air, ie: inhaling it), but it has never been proven that she contracted the virus though aerosol contamination.  The Zaire Mayinga strain is the ONLY Ebola strain that has ever been even suspected of being transmitted through aerosol contamination, and it is extremely rare.  To the best of my knowledge, the Mayinga strain hasn’t been seen in an outbreak since 1978.

ALL the strains of Ebola, and Marburg viruses are very very contagious through membrane transmission ie: through direct contact with liquid particles (blood, mucous, semen, sweat, urine) onto mucous membranes or through open wounds.  This means that if you physically come into contact with liquid particles infected with an Ebola virus through your mouth, eyes, nose, genitalia or an open wound, then you have a very large probability of being infected with the virus.   Hence: it is highly contagious though PHYSICAL contact with the infected bodily liquids of someone who has the virus.  ie: though touching the body/body fluids, contact with the sheets, bandages, needles, medical instruments etc of an infected person.

BUT….. the virus doesn’t not live very long outside of a human or animal host.   ALL Hemorrhagic fever viruses (all strains of Ebola, Marburgs etc…) are actually very fragile virus particles that need a very specific environment to survive for even a short time.  THIS is why all cases of Ebola always happen in the same place, in Central/West African jungles:  HOT HOT HOT and WET WET WET.  ALL Hemorrhagic viruses require extreme heat and humidity to survive, and as I said above, they literally die very quickly when they are exposed to air conditioning.

These are two of the main reasons that “they” were not able to weaponize Ebola before: because it requires direct contact with infected bodily fluids AND it dies very quickly when it comes in contact with drier, cooler air.

One of the other reasons that they were not able to weaponize Ebola is because it kills too quickly and the gestational period is too short for it to spread very far.  Ebola Zaire has the highest mortality rate- close to 90% of those infected die from the virus, but it also has the shortest gestational period and it can be symptomatic as quickly as 2-6 days after contamination.  As the onset of symptoms is so severe immediately, infected people are not likely to be boarding airplanes, going to night clubs or partaking in unprotected sex.

Marlburg virus is another form of Hemorrhagic fever that “they” have played with, but while it has a longer gestational period- close to 2-3 weeks- it also has a much lower mortality rate that varies wildly between 20-80%…..

The tampering of these viruses needed to make them a viable bio weapon is something they’ve been “working on” for at least 40 years.

….. And here is the proof of “their” work:

http://www.google.com/patents/US20120251502

Human Ebola Virus Species and Compositions and Methods Thereof

US 20120251502 A1\

Publication number US20120251502 A1
Publication type Application
Application number US 13/125,890
PCT number PCT/US2009/062079
Publication date Oct 4, 2012
Filing date Oct 26, 2009
Priority date Oct 24, 2008
Also published as CA2741523A1, EP2350270A2, EP2350270A4, WO2010048615A2, WO2010048615A3
Inventors Jonathan S. Towner, Stuart T. Nichol, James A. Comer, Thomas G. Ksiazek, Pierre E. Rollin
Original Assignee The Government of the US as Represented by the Secretary of the Dept. of health
Export Citation BiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet

All of the information that is contained in this patent is important and worth reading, even though the information is difficult to wade though unless you have some understanding of medical terminology that is used in these type of documents.  It’s also a lesson on reading what they are actually saying in amongst the mumbo jumbo.  I’ve highlighted a few sentences that are very telling from a small excerpt of the document.

In another aspect, the invention provides vaccine preparations, comprising the inventive hEbola virus, including recombinant and chimeric forms of the virus, nucleic acid molecules comprised by the virus, or protein subunits of the virus. The invention also provides a vaccine formulation comprising a therapeutically or prophylactically effective amount of the inventive hEbola virus described above, and a pharmaceutically acceptable carrier. In one embodiment, the invention provides a vaccine formulation comprising a therapeutically or prophylactically effective amount of a protein extract of the inventive hEbola virus described above, or a subunit thereof; and a pharmaceutically acceptable carrier.\….\

… According to the present invention, the chimeric viruses are encoded by the viral vectors of the invention which further comprise a heterologous nucleotide sequence. In accordance with the present invention a chimeric virus is encoded by a viral vector that may or may not include nucleic acids that are non-native to the viral genome. In accordance with the invention a chimeric virus is encoded by a viral vector to which heterologous nucleotide sequences have been added, inserted or substituted for native or non-native sequences. In accordance with the present invention, the chimeric virus may be encoded by nucleotide sequences derived from different species or variants of hEbola virus. In particular, the chimeric virus is encoded by nucleotide sequences that encode antigenic polypeptides derived from different species or variants of hEbola virus.”

chi·me·ra

kīˈmi(ə)rə,kə-/

noun

noun: chimera; plural noun: chimeras; noun: chimaera; plural noun: chimeras; noun: Chimera

  1. 1.(in Greek mythology) a fire-breathing female monster with a lion’s head, a goat’s body, and a serpent’s tail.
    • any mythical animal with parts taken from various animals.

    2.

    a thing that is hoped or wished for but in fact is illusory or impossible to achieve.

    “the economic sovereignty you claim to defend is a chimera”

Chimera

Mythical creature

The Chimera was, according to Greek mythology, a monstrous fire-breathing hybrid creature of Lycia in Asia Minor, composed of the parts of three animals – a lion, a snake and a goat.Wikipedia\

“They” go to great lengths to create the illusion that this patent is for the creation of a vaccine to protect against Ebola… but you can’t create a vaccine for a virus unless it is for THAT SPECIFIC VIRUS.  Plain english:  You have to create the “chimeric” virus in order for the “chimeric” virus based vaccine to work!! This means that if they are creating a vaccine from multiple viruses, the vaccine will only work for that CREATED virus.   This is the ongoing mythology of the yearly flu vaccine:  they create a vaccine that will only work on 2 or 3 strains of “flu” virus, but unless they know exactly which strain of flu is going to “appear” that year, the vaccine is completely useless!  There are literally thousands of strains of the “flu” virus, hence unless they know exactly which one is going to  be let loose in the public, they cannot produce a vaccine that has any ability to do anything (…. except spread the virus further though live virus vaccines of course).

This Patent is for a man made form of Ebola- one that has been created by combining several other viruses.  I won’t post it all here as it would make this article incredibly long, but if you’d like to do some homework, do a google search on the names and previous work of the inventors of this hybrid chimeric virus, and check out their other areas of study and research (polio and the common cold? hmmmmm).

Next up to research: who is running the patent.  Who is buying up the license to distribute the virus or the vaccine?  (did you know that Rumsfeld is the global license holder for the H1N1 vaccine?) and who are the agents (usually a law firm) for the patents?  In Canada it is Ridout & Maybee LLP……  seriously? ….. And also look for any private offerings (investment offerings) by those agents that would enable funding the $800 billion to $1 trillion FDA bribe…I mean “price tag”…I mean “application and processing fees”…tee hee…and the subsequent “derivative market”/exchange traded fund to pay back all those sucker “institutional investors” who shove off the liabilities to the secondary markets and the public investors on main street…… bwuhaaaahaaaaahaaaaa!!!  Wait!!!!!!  No worries, the “investors” are still busy trying to figure out how to process the gold, silver, and metals molestation with Basel III promising a “new gold-backed financial system”….toooo much fun!!!!!!!!  Hollywood seriously can’t write stories like this!….  that last bit was written by Heather, who hijacked my computer for a few moments.

This Ebola “pandemic” that is purportedly happening in 4 countries in Africa – 3 of which have never had an outbreak of Ebola before: Liberia, Guinea and Sierra Leone- is very blatantly NOT acting like Ebola outbreaks usually do.  First off, considering the “infected” numbers that were given in Feb 2014 at the beginning of this “outbreak”, and the supposed spread of the virus to 3 other countries…. not enough people have died.  I know that that is a morbid thing to say, but the Ebola virus kills very quickly, with a high mortality rate and IF the virus was in large city centres as the media is saying, and IF the virus was being spread through aerosol transmission as the media is saying, and IF the virus is getting onto airplanes and getting to Canada and the US and Europe as the media was saying was happening in late February 2014…. then WAY WAY WAY  more people should of already have died from this “pandemic”.

The World Health Organization has released statistics that Prove that the media is hyping up the fear porn.  See the Jon Rappoport article quoted below……. the numbers do NOT add up. Not even slightly.

A few more interesting facts about this Ebola outbreak:

Initial outbreak in Guinea

In February 2014, the first Ebola virus outbreak registered in the region occurred in Guinea. By 23 April, the total number of suspected and confirmed cases in the Ebola virus disease (EVD) outbreak had increased to 242, including 142 deaths at a fatality rate of 59%.[5] Originally, the suspected cases were reported in Conakry (four cases), Guéckédougou (four), Macenta (one) and Dabola (one) prefectures. On 25 March the Ministry of Health of Guinea reported that four southeastern districts—Guekedou, Macenta, Nzerekore, and Kissidougou—were affected with an outbreak of Ebola virus disease.[6] The following day the Pasteur Institute in Lyon, France confirmed the Ebola strain as Zaire ebolavirus.[6] An initial report suggested that it was a new strain of ebolavirus,[7] but this was refuted by later studies which placed it within the lineage of the Zaire strain.[8]\

http://en.wikipedia.org/wiki/2014_West_Africa_Ebola_outbreak\

Diagnostic methods for IDing Ebola in those 3 countries are uncertain. Therefore, we should only consider the category labeled “confirmed,” and even then we should have doubts.
So let’s look at the total for confirmed Ebola case numbers in those countries.
It’s 814.
Confirmed number of deaths? 456.
Now consider another WHO report. This one is titled: “Influenza (Seasonal) World Health Organization,” dated April 2009.
It’s the WHO fact sheet on regular seasonal flu, the kind that is said to infect people globally, year after year, like clockwork.
Ready?
Annual number of severe cases: 3-5 million.
Annual number of deaths: between 250,000 and 500,000.
Remember, that’s every year—not a one-time shot.

http://jonrappoport.wordpress.com/2014/07/31/is-it-ebola-or-is-it-psychological-warfare/

Tekmira Pharmaceuticals Corporation (TKMR) (TKM.TO), a leading developer of RNA interference (RNAi) therapeutics, announced today that it has received a $1.5 million milestone payment from Monsanto following completion of specified program developments.

http://finance.yahoo.com/news/tekmira-receives-1-5-million-230000330.html

About TKM-Ebola, an Anti-Ebola Virus RNAi Therapeutic

TKM-Ebola, an anti-Ebola virus RNAi therapeutic, is being developed under a $140 million contract with the U.S. Department of Defense’s Medical Countermeasure Systems BioDefense Therapeutics (MCS-BDTX) Joint Product Management Office. Earlier preclinical studies were published in the medical journal The Lancet and demonstrated that when siRNA targeting the Ebola virus and delivered by Tekmira’s LNP technology were used to treat previously infected non-human primates, the result was 100 percent protection from an otherwise lethal dose of Zaire Ebola virus (Geisbert et al., The Lancet, Vol 375, May 29, 2010). In March 2014, Tekmira was granted a Fast Track designation from the U.S. Food and Drug Administration for the development of TKM-Ebola.

http://finance.yahoo.com/news/tekmira-provides-tkm-ebola-phase-161928543.html

What we are seeing is a man made virus being used (luckily not very successfully when you consider the virus they are working with) on an unsuspecting population as a means to drive the public into a fear spiral of desperation, to allow them to promote “their” martial law scam (you know… the one that hasn’t worked for them yet?), and to create a vaccine hysteria to create the illusion of money being in circulation and strengthen the seriously lagging reputation of the worlds main medical institutions and agencies.   This is a DISTRACTION.

D I S T R A C T I O N

Final word on Viruses in general:   Do you know how many Viruses modern science and medicine has been able to cure?

Zero

Do you know how many Viruses have been eradicated with medicines or vaccines?

Zero

Yet…. we are all still here.

Source: http://www.removingtheshackles.blogspot.ca/2014/08/the-ebola-outbreak-pandemic-that-isnt.html