Now they’re going to vaccinate infants too

Lena Svensson DigDeepNews Nov 13 2009

FDA Expands Approved Use of H1N1 Vaccines to Include Infants and Children

But what are the dangers in vaccinating small children?

Vaccines and infants

SIDS and vaccines

The Truth Behind the Vaccine Cover-Up says:

 

It takes them awhile to get the two forms of mercury straight, since for several pages of the report they say methylmercury is in thimerosal rather than ethylmercury. They can be forgiven for this. On page 16, Dr. Johnson, an immunologist and pediatrician at the University of Colorado School of Medicine and the National Jewish Center for Immunology and Respiratory Medicine, notes that he would like to see the incorporation of wide margins of safety, that is 3 to 10-fold margins of safety to "account for data uncertainties." What he means is that there are so many things we do not know about this toxin that we had better use very wide margins of safety. For most substances the FDA uses a 100-fold margin of safety.

The reason for this, which they do not mention, is that in a society of hundreds of millions of people there are groups of people who are much more sensitive to the toxin than others. For instance, the elderly, the chronically ill, the nutritionally deficient, small babies, premature babies, those on certain medications and inborn defects in detoxification, just to name a few. In fact, in this study they excluded premature babies and low birth weight babies from the main study, some of which had the highest mercury levels, because they would be hard to study and because they had the most developmental problems related to the mercury.

The article goes on to say:

In fact, on page 163, Dr. Robert Brent, A developmental biologist and pediatrician at the Thomas Jefferson University and Dupont Hospital for Children, says that we don't have data showing accumulation and "that with the multiple exposures you get an increasing level, and we don't know whether that is true or not." He redeems himself somewhat by pointing out that some of the damage is irreversible and with each dose more irreversible damage occurs and in that way it is accumulative.

In other words, you may have been “fine” getting all those other vaccinations, but that next one might be the one that causes sudden, irreversible damage.

Several times throughout this conference, Dr. Brent reminds everyone that the most sensitive period for the developing brain is during the early stages of pregnancy. In fact, he pinpoints the 8th to 18th week as the period of neuromaturation. In fact, the most rapid period of brain maturation, synaptic development and brain pathway development is during the last three months of pregnancy continuing until two years after birth. This is often referred to as the "brain growth spurt." This is also not mentioned once in this conference, again because if mothers knew that their child's brain was busy developing for up to two years after birth they would be less likely to accept this safety of mercury nonsense these "vaccinologists" proclaim.

And then we have Aluminum phosphate:

In a study of some 92 patients suffering from this emerging syndrome, eight developed a full-blown demyelinating CNS disorder (multiple sclerosis). [Authier FJ, Cherin P, et al. Central nervous system disease in patients with macrophagic myofasciitis. Brain 2001; 124: 974-983.] This included sensory and motor symptoms, visual loss, bladder dysfunction, cerebellar signs (loss of balance and coordination) and cognitive (thinking) and behavioral disorders.
Dr. Gherardi, the French physician who first described the condition in 1998, has collected over 200 proven cases, One third of these develop an autoimmune disease, such as multiple sclerosis. Of critical importance is his finding that even in the absence of obvious autoimmune disease there is evidence of chronic immune stimulation caused by the injected aluminum, known to be a very powerful immune adjuvant.
The reason this is so important is that there is overwhelming evidence that chronic immune activation in the brain (activation of microglial cells in the brain) is a major cause of damage in numerous degenerative brain disorders, from multiple sclerosis to the classic neurodegenerative diseases (Alzheimer's disease, Parkinson's and ALS). In fact, I have presented evidence that chronic immune activation of CNS microglia is a major cause of autism, attention deficit disorder and Gulf War Syndrome.
Dr. Gherardi emphasizes that once the aluminum is injected into the muscle, the immune activation persists for years. In addition, we must consider the effect of the aluminum that travels to the brain itself. Numerous studies have shown harmful effects when aluminum accumulates in the brain. A growing amount of evidence points to high brain aluminum levels as a major contributor to Alzheimer's disease and possibly Parkinson's disease and ALS (Lou Geherig's disease). This may also explain the 10X increase in Alzheimer's disease in those receiving the flu vaccine 5 years in a row. (Dr. Hugh Fudenberg, in press, Journal of Clinical Investigation). It is also interesting to note that a recent study found that aluminum phosphate produced 3X the blood level of aluminum, as did aluminum hydroxide. (Flarend RE, hem SL, et al. In vivo absorption of aluminum-containing vaccine adjuvants using 26 Al. Vaccine 1997; 15: 1314-1318.)

As for infants, they have no immune response that can use the “benefits” of vaccines, therefore they receive no real protection against what you’re vaccinating against. Oxford Study--No Evidence Flu Vaccine works in infants