Stanford researchers confirmed mRNA vaccines trigger myocarditis via a
two-step inflammatory cascade—CXCL10 recruits immune cells, followed by
IFN-gamma, which damages heart tissue, creating a vicious cycle of
inflammation.
Beyond inflammation, the vaccine's spike
protein infiltrates heart cells, causing autoimmune attacks (molecular
mimicry), with lingering spike proteins detected in myocarditis victims'
cardiac tissue.
Young males face disproportionate harm due
to testosterone exacerbating inflammation, while estrogen may be
protective—evidenced by military data showing myocarditis cases within
days of vaccination.
Pfizer's leaked documents and
independent studies prove prior knowledge of myocarditis risks, yet
CDC/FDA downplayed them, ignored military warnings and maintained
mandates without adequate safety monitoring.
Soy-derived
genistein blocked heart damage in mice, exposing the absurdity of
needing "fixes" for a flawed product. Critics demand accountability for
trial flaws, censorship and the broader pattern of vaccine injuries
(blood clots, infertility, neurological harm) suppressed by authorities.
A
groundbreaking study from Stanford University has confirmed that
COVID-19 mRNA vaccines trigger myocarditis—a potentially
life-threatening heart inflammation—through a two-step inflammatory
process driven by specific immune chemicals. Published this week, the
research sheds light on a phenomenon that has been dismissed or
downplayed by health authorities despite mounting evidence from military
data, leaked Pfizer documents and independent medical reports....<<<Read More>>>...
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