This story simply does not make sense.
FIRST: - It claims "Tens of thousands of Canadians were infected with AIDS" (by infected blood).
The problem with this statement is that THE TOTAL number of people with a '"positive 'AIDS' diagonisis"
between 1983 and 1994 in Canada was only 12,216.
Even if only ONE 'ten(s) of thousand' had been so infected it would account for almost ALL of the total 'AIDS' cases in Canada.
TWO. Blood transmission is very rare (if you believe the HIV hypothesis in the first place). Dr. Willner who injected 'HIV' seven times suffered no ill effects and tens of thousands of needle stick accidents have resulted in almost no 'AIDS' infections.
It is strange how the media buys into these exaggerated scare stories without even doing a quick check to see if the figures add up.
HERE IS ANOTHER FACT ABOUT CANADA
Cumulative 'AIDS' figures in Canada
What is interesting is that there have only been 65 teenage cases since 1983 in Canada. Also the 20 to 25 age group is very low too.
This is similar to the U.S. and does not fit an std.
Like America, people over 60 have as much 'AIDS'
(611 cases) as both teenagers AND 20-24 years olds combined (65 teen cases and 573 cases in the 20-24 group).
Seems once again Grannies Gone Wild!
Check the facts for yourself at: -
http://www.avert.org/canstatr.htm
BLOOD TRANSMISSION REMAINS UNPROVEN
To date, there is no evidence of the existence in human plasma of particles with the morphological characteristics attributed to HIV even though the plasma of at least some "HIV infected" individuals is claimed to contain such particles.
Thus Levy, whose team reported most often on the relationship between HIV and factor VIII wrote in 1988: "Human Immunodeficiency virus in plasma or serum has been found in about 30% of specimens from seropositive persons, generally at a concentration of less than 10 IP/mL12" [IP=3Dinfectious particles] (Levy, 1988). Reference 12 cited by Levy is a paper which he published in collaboration with Barbara Michaelis but this paper does not contain a description of the method used to show that (a) HIV seropositive (non-haemophiliac) plasma was infected with "HIV particles"; (b) HIV was "present in low titers"; (c ) the particles were "infectious". Commenting on his and his colleagues' findings Levy wrote: "These studies demonstrate further that not all seropositive individuals have virus recoverable from their PMCs and that isolation from serum is not a common event" [PMCs=peripheral blood mononuclear cells] (Michaelis & Levy, 1987). "Thus, cell-free virus in body fluids is unlikely to be a meaningful source of HIV transmission". (Levy, 1988).
At least one other eminent HIV/AIDS researcher is also of the opinion that HIV cannot be transmitted through "...products prepared from blood, such as albumin, plasma, protein fractions, or hepatitis B vaccine" (Blattner, 1989). If HIV cannot be transmitted through "cell-free" body fluids (plasma) because it is not found in the plasma of 70% of seropositive individuals and in the remaining 30% is "generally at a concentration of less than 10 IP/mL", then it will be even less probable that factor VIII prepared from plasma can be a "meaningful source of HIV transmission" since, even if HIV were present in a plasma collection, it would be diluted many times over during the process of factor VIII manufacture.
This is because factor VIII is made by pooling plasma obtained from 2000 to 30,000 individuals amongst whom at most, there will be only a few HIV seropositives. Since factor VIII prepared from large batches of pooled plasma is ultimately shared amongst many haemophiliacs, the load of HIV for each haemophiliac will be substantially lower than 10 IP/ml.
Since 1989, detection of a 24,000 molecular weight protein (p24) in cell cultures, (T cells from persons presumed to be infected), or co-cultures, (of T cells from persons presumed to be infected, with T cells from normal individuals), has been used to quantify HIV in cells, "cellular viremia" (Masquelier et al., 1992). Detection of p24 in cultures of T cells from normal individuals with plasma from those presumed to be infected has been used to quantify HIV in plasma, "plasma viremia" (Coombs et al., 1989; Ho et al., 1989; Clark et al., 1991).
There are many reasons why p24 cannot be used to quantitate or even detect the presence of "HIV infectious particles".
These include:
(a) there is ample evidence that the p24 protein is not HIV specific (Papadopulos-Eleopulos et al., 1993a and see below);
(b) there is no relationship between plasma viraemia, cellular viraemia (p24 in culture), and the titre of p24 in (uncultured) plasma (HIV antigenaemia). "Only 45 percent of patients with plasma viremia had HIV p24 antigen in either serum or plasma" (Coombs et al., 1989). "Plasma p24-antigen titres before or after acidification did not show any significant correlation with quantification by tissue culture method" (Weber & Ariyoshi, 1992).
Nor does correlation exist between the "most specific" HIV antibody test, the Western blot (WB), and plasma p24. With methods which have a reported lower limit of sensitivity of 10-50pg/ml, p24 can be detected in only 12% of HIV positive sera (Jackson et al., 1989);
(c) "Much of the viral protein secreted from HIV-infected cells is non-particulate, and the proportion of (for example) p24 in virions is a function of the viral genotype and the age of the culture. In extreme cases, less than one percent of the total p24 and gp120 present is in virions" (McKeating & Moore, 1991). [It must be pointed out that in the AIDS literature, the terms "HIV", "HIV isolation", "pure particles", "virus particles", "virions" and "infectious particles", have a variety of meanings and include all of the following, but most often without proof of the presence of a particle: (i) "RNA wrapped in protein"; (ii) material from the cell culture supernatants which passes through cell tight filters but through which organisms such as mycoplasmas may pass; (iii) the pellet obtained by simple ultracentrifugation of the culture supernatant; (iv) recently, very often, detection in AIDS cultures of p24 (Papadopulos-Eleopulos et al., 1993a)].
In the process of preparing plasma for factor VIII extraction, great care is taken to exclude cells. Even if some cells are inadvertently present, it would be most unlikely that they would constitute "a meaningful source of HIV transmission" since, like "HIV particles", "infected" cells present in the plasma of a seropositive donor would be diluted many times over by the plasma and cells from the manifold number of non-seropositive donors from which factor VIII is made.