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PEMF Relief, ER Drug Screens, and Untreated Disability

Day 1 · 6:15:32 · Kevin Street · Dean Allison

  • 📡 Peter McCullough protocol and pulsed electromagnetic frequency (PEMF) reduced inflammation and improved function when he could access them.
  • 🏥 Early ER visits screened him for meth and opioids as an overdose; critical treatment window slipped away until Ottawa Civic.
  • ♿ Accepted to KITE disability program that cannot fix him; therapies are uncovered and he was treated as a stroke patient then dropped for lack of progress.

Self-funded protocols versus system misdiagnosis and denial of care.

← Violent Full-Body Tremors and Thirteen Brain Lesions | VISP File Lost Twice After Four Years of Waiting →

Transcript

Speaker L · 6:15:32

Thanks for your story, Kevin. Uh, you had said you've, uh, tried a few protocols that seem to help. What, what have you found is helping?

Kevin Street · 6:15:42

Um, so we, we tried every protocol I think that's been crossed over the table. Obviously everything Everything is expensive to do and try. I did do the Peter McCullough protocol for about a year, and I used that simply because my blood is in bad shape. So I did that. And we've also found that a lot of frequency, believe it or not, seems to help a lot, especially with inflammation and inflammation on my brain. Obviously, your brain is one of those places that you can't massage and you can't get at. And for whatever reason, this technology that we've found, which is PEMF or pulsed electromagnetic frequency, in the dose that we're taking it in, has been helping substantially. And it removes a lot of the inflammation within my body, especially in my brain.

Kevin Street · 6:16:46

And when I do that I can function a lot better.

Speaker L · 6:16:52

And so you're obviously getting medical attention and medical practitioners are paying attention to you. Are you satisfied with the help that you're getting?

Kevin Street · 6:17:01

Well, that's a difficult question. So the first, first four weeks of my visits to the emergency room, they kept testing me for methamphetamines and opioids. And, and, uh, all kinds of nasty drugs because I was presenting, um, as obviously an overdose. Um, I—.

Speaker D · 6:17:25

They—.

Kevin Street · 6:17:25

It's just, it went on and on. So the, the initial period where they could have potentially treated me for my condition was, was literally just being— it was slipping away. And my wife knew it, and she was witnessing it. And I remember we were at the hospital and, and I went in to see my, my family physician after I had seen her in the emergency room and found out that she was testing me for these things, knowing that I'm not that person. And, uh, and, uh, that was when my wife said to me, we need to go, we need to go to a different hospital, we need to go to a major hospital and find somebody who knows or has at least seen something like this. So we came to Ottawa and we went to the Ottawa Civic and, and I was put into a ward with like at least 20, 25 people that were all ill. And these weren't COVID patients, guys. These were, these were people that were making presentations like myself.

Kevin Street · 6:18:29

And that was when I met my first neurologist and and now I have— I've just finally been accepted to a, uh, a program called, uh, KITE, which is supposedly the best in the world, uh, for my, for my disability. Uh, they cannot fix my disability. I'm permanently disabled. They don't know what or how, uh, to do, but all they can offer me are things to try and make me live a little bit easier. So the unfortunate part about that is these treatments, again, as everyone knows, they're not covered. So, so we need to figure that out, and we need to figure out why these things are this way. I, I have to come up with different— what's the word I'm looking for? I need to be diagnosed with other things in order to get certain types of attention.

Kevin Street · 6:19:30

Hence, I now have sugar diabetes, and with my diabetes, I now have access to some types of therapies because that particular condition will allow you to get access to therapy. The problem is, guys, is I've been waiting for a phone call from that therapy that they promised me for over 2 years now, and I just found out on less than a week ago— my memory is horrible, but it was one of the days last week where I received a phone call from Toronto again to tell me that once again I'm not, uh, they're not able to fulfill my, my appointment and we need to rebook again. So I'm now, well, like I said, what was it, 1,951 days, and I haven't received any type of treatment that is directed at my disability. They did attempt a 9-week therapy session that was supposed to be 12, but they removed me from it because I wasn't showing any progress, and they weren't treating me for the proper condition either.

Kevin Street · 6:20:35

They were treating me as a stroke patient.

Dean Allison · 6:20:37

Yeah, but so can I just jump in?