Impact of Vaccines on Cancer Treatment
Give evidence on this. I'd just like to point out
that I have done, as you
say, I've been in cancer immunotherapy,
I've been in cancer immunotherapy for over three decades,
and, uh, I have made, uh, big advantage- advances in the
treatment of cancer with immunotherapy.
So this sets the scene that I then be- I became
aware in, uh, early '20, uh, two
of my patients who'd been, uh, stable for years, uh,
do mainly melanoma patients. They'd had several different types of
immunotherapy, and in six weeks I saw six
patients relapse with melanoma. They had, uh, they'd been
stable for three to eighteen years.
They felt well, apart from the relapse, and being
investigated. I asked, you know, what was the thing
that was common? And the thing that was common is they'd all
received a booster vaccine from their general
practitioners. Now I know that these cancers
are c- totally controlled by the T-cell response,
so I immediately
suspected the T-cell response was being perturbated
by the cancer. And initial, uh,
investigations showed that this was likely to be true.
However, there was then a paper published by
some p- uh, doctors in Madrid, which, and I quote,
their paper is called The Evidence of Exhausted Lymphocytes
After the Third Anti-SARS COVID 2 Vaccine Dose in
Cancer Patients. I mean, this was absolutely
staggering that they showed across hundreds of patients that you get
this T-cell suppression. Hot on the heels of this were then a
numerous reports that the, uh, following a booster
vaccine, we were getting IgG immunoglobulin
switching, so you converted the immune system from
being
aggressive fighting invaders to one of tolerization.
So therefore, the immune system was tolerating the cancer,
and this was the reason you were starting to see it.
However, it is important at this stage to say
that we were getting
reports after I first reported this of other cancers.
And my initial observation that this was all due to T-cell
suppression started to, um, fade in-
into the, uh, perspective that other a- actors were at work with
the vaccine, as it were. Colorectal cancer was being
reported by my patients, by my, uh, fellow surgeons
as reporting, uh, as, uh, presenting late,
stage four, not stage one or two, and early in, in
patients in their twenties and thirties and forties in a way
that we've not
seen before. And then in my own practice, as I was
looking for patients, uh, w- who had co- um, who'd had
other cancers, I noticed that they too had had
booster vaccines, and I list them in my report.
They go from everything from the common cancers, from breast,
prostate, et cetera, and all the way through to some really
unexpected ones, including glioma and more
recently hematological malignancies.
Now looking at the, uh, literature as to why this,
uh, could be, and I'm involved in pres- uh, two big publications.
One's we accepted prior to,
uh, um, uh, prior to, um, changes. And this shows that there are
remarkable at least a dozen mechanisms where messenger
RNA can insert into the DNA and
activate oncogenes, and more importantly, in the
especially the long term, they can suppress, uh, the
suppressor networks, which means if a cancer is starting to
evolve, it would normally be maintained, uh, controlled,
and, uh, this a- mechanism is being prevented.
And the number of people who've shown this is quite enormous.
So as an oncologist who I started to see that it's
not only my patients now, it's people I know really well who
are going down with cancer, and they're going down more aggressively,
and the treatment is not working nearly as well.
And I'm used to people saying, "Oh, there's no evidence that the cancer's
increasing and that there's anything to do with the vaccine." But
I can assure you from the patients that I have seen, that many have
seen, uh, a dozen doctors before. Not one of
them has ever asked the vaccine history.
So of course they see no evidence. And my full
detailed research into the messenger RNA vaccines, and I was
on the scientific board of a company claimed to be the messenger RNA
vaccine, uh, company for five years.
I left eight years ago. So I know a lot more than the average
clinician.
And ma- myself and others feel that there is no
way you can control this technology and its use for future
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