Let's talk about this shot because something has happened that I believe will change the conversation

around the vaccine reporting perhaps forever, hopefully forever.

So let's look at what happened in the UK here.

Just recently this headline came out.

Now, the MHRA is their medicines regulator.

It's like our FDA.

So this is the headline here,

Medicines regulator failed to flag COVID vaccine side effects and must be investigated, says MPs.

And it says some 25 members of parliament across five parties have written to the Health Select

Committee asking for an urgent investigation.

In reply, Steve Bryan, the Health Committee Chairman, has said an inquiry into patient safety

is very likely.

In a letter to Mr. Bryan, the APPG said that there was reason to believe that the

MHRA had been aware of post vaccination heart and clotting issues as early as

February 2021 but did not highlight the problems for several months.

When I saw that, I went, wait a minute,

that sounds familiar because the CDC did the same thing.

So this is the headline when the CDC did it.

This is CDC drafted alert for myocarditis, a public alert.

Imagine that, they're going to try that.

And COVID-19 vaccines, but never sent it.

So you have this shot that has been rolled out. You have these medicine agencies,

...