Is there evidence linking SIDS to vaccines?
Although some studies were unable to find correlations between SIDS and vaccines,22–24 there is some evidence that a subset of infants may be more susceptible to SIDS shortly after being vaccinated. For example, Torch found that two-thirds of babies who had died from SIDS had been vaccinated against DPT (diphtheria–pertussis–tetanus toxoid) prior to death. Of these, 6.5% died within 12 hours of vaccination; 13% within 24 hours; 26% within 3 days; and 37%, 61%, and 70% within 1, 2, and 3 weeks, respectively. Torch also found that unvaccinated babies who died of SIDS did so most often in the fall or winter while vaccinated babies died most often at 2 and 4 months—the same ages when initial doses of DPT were given to infants. He concluded that DPT “may be a generally unrecognized major cause of sudden infant and early childhood death, and that the risks of immunization may outweigh its potential benefits. A need for re-evaluation and possible modification of current vaccination procedures is indicated by this study.”25 Walker et al. found “the SIDS mortality rate in the period zero to three days following DPT to be 7.3 times that in the period beginning 30 days after immunization.”26 Fine and Chen reported that babies died at a rate nearly eight times greater than normal within 3 days after getting a DPT vaccination.27
Ottaviani et al. documented the case of a 3-month-old infant who died suddenly and unexpectedly shortly after being given six vaccines in a single shot: “Examination of the brainstem on serial sections revealed bilateral hypoplasia of the arcuate nucleus. The cardiac conduction system presented persistent fetal dispersion and resorptive degeneration. This case offers a unique insight into the possible role of hexavalent vaccine in triggering a lethal outcome in a vulnerable baby.” Without a full necropsy study in the case of sudden, unexpected infant death, at least some cases linked to vaccination are likely to go undetected.28e by Neil Z Miller and Gary S Goldman
Conclusion by Neil Z Miller and Gary S Goldman
The US childhood immunization schedule requires 26 vaccine doses for infants aged less than 1 year, the most in the world, yet 33 nations have better IMRs. Using linear regression, the immunization schedules of these 34 nations were examined and a correlation coefficient of 0.70 (p < 0.0001) was found between IMRs and the number of vaccine doses routinely given to infants. When nations were grouped into five different vaccine dose ranges (12–14, 15–17, 18–20, 21–23, and 24–26), 98.3% of the total variance in IMR was explained by the unweighted linear regression model. These findings demonstrate a counter-intuitive relationship: nations that require more vaccine doses tend to have higher infant mortality rates.
Efforts to reduce the relatively high US IMR have been elusive. Finding ways to lower preterm birth rates should be a high priority. However, preventing premature births is just a partial solution to reduce infant deaths. A closer inspection of correlations between vaccine doses, biochemical or synergistic toxicity, and IMRs, is essential. All nations—rich and poor, advanced and developing—have an obligation to determine whether their immunization schedules are achieving their desired goals.
IMR = infant mortality rate
the FCC mentioned here is actually the Forensics Center of Cincinnati , Ohio
When no one at the point of injection knows how to authenticate what is in the vial , then every injection is pancuronium bromide ( the second injection of a lethal injection cocktail in prison)
Click on Pictures for links !
Why is it that infant mortality rates seem to be higher at 2 , 4 , and 6 months old ?
If you take the needle that the perpetrator is trying to inject into your child, and inject it into the perpetrator instead ?
causing their death, are you guilty for murder ? .
There are 4 stages of immune response
1st Cytokine or inflammation that is triggered by a CD+4 homing beacon neuron trigger from either the Epidermal or Mucosa immune system, it is meant to stop any poison from distributing through the body and or to stop any further injury to a broken bone or laceration in the skin.
2nd Leukocyte production and delivery to the affected area for the mechanics of repair and disease, viral and bacterial remediation.
The white blood cells can actually rebuild points of the entire body if need be.
3rd Increased temperature as the leukocytes actually function better at between 102 and 104 degrees, this is critical to the immune system function as secondary reactions from the thermal increase promote rebuilding of cells in the body.
4th Random Increased Heart Rate as this delivers more white blood cells to the affected area, it is random as the red blood cell carries the Adenosine Triphosphate the fuel for the muscles to function and is in lesser quantities as the white blood cells are dominant by ratio.
If you have a pounding headache, whole body is sore, a fever, racing heart rate ? Your immune system is trying to fix something and do not suppress any of those functions or you will not fix the problem that started it in the first place, if your High Density Lipoproteins level is below 200 and your Sodium count is way low ? Then your immune system is not functional . The HDL in your blood is the taxi for the immune systems D3 or macrophage to get to the problem area, once the Macrophage do their job and create a byproduct from digesting the virus or bacteria, that waste also gets transported by the HDL in the blood to the Lymphatic glands that filter out the toxins and attach it to sodium for transport out of the body with water via the epidermis a.k.a. sweat glands .