Woods: 23 Canadian Doctors Mock, Refuse Tests; US Confirms SFN & POTS¶
Day 3 · 6:58:17 · Shawn Buckley · Julie Woods · Crystal Denomme · Dean Allison
- 🗣️ Father and daughter saw 23 Canadian doctors who called her stupid, incompetent, a drug addict or pure psych case.
- 🇺🇸 October 2024 Utah trip finally diagnosed small-fiber neuropathy, POTS, mitochondrial dysfunction, insulin resistance and microclots.
- 🧪 Canadian specialists refused the very tests React19 peers had taught her to request.
Years of Canadian medical abuse forced private U.S. diagnosis of multiple post-vaccine conditions.
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Transcript¶
Shawn Buckley · 6:58:17
The, um, you were talking about getting diagnosed in the States.
Julie Woods · 6:58:21
Yes.
Shawn Buckley · 6:58:21
Um, and it, it's really interesting that somebody in Canada has to pay privately to go to the States to get diagnosed. What year, when was it? Like what month and year did you end up going to the States?
Julie Woods · 6:58:35
It was October of 2024 that I went to Utah.
Shawn Buckley · 6:58:40
Okay, so you're, you're injured in 2021.
Julie Woods · 6:58:43
Yes.
Shawn Buckley · 6:58:44
And the Canadian medical system will not give you a proper diagnosis, and you end up in 2024 going to the States.
Julie Woods · 6:58:54
Uh, yes, correct. My dad and I traveled up to 10 hours, uh, to see a total of 23 doctors in Canada to try to get my condition properly assessed. Diagnosed and to obtain treatments. Unfortunately, the responses that we received in Canada ranged anywhere from being called stupid and incompetent and being told that vaccines don't do that and that I needed to stop wasting the time of the medical community. And when my condition was finally acknowledged by someone in Canada, the response was that I should be thankful because other people reacted far worse than I did. So either my condition was not acknowledged or my condition wasn't bad enough to be treated.
Shawn Buckley · 6:59:52
I just, I just want to unpack this because I, I think we need to slow it down just so that it can sink in for people. So you and your father, because you now have to rely on your parents Yes. You can't cook meals by yourself. You cannot go to the store by yourself. You cannot go to medical appointments by yourself. You're no longer independent.
Crystal Denomme · 7:00:13
That's correct.
Shawn Buckley · 7:00:15
And so relying on your, your parents, you go to 23 doctors.
Julie Woods · 7:00:21
Yes.
Shawn Buckley · 7:00:22
Basically to get help and get diagnosis and tests in Canada. You As I'm, you know, from an earlier conversation. Yeah. So one, a neurologist instructed a nurse to, quote, tell that girl that vaccines don't do that.
Julie Woods · 7:00:40
Yes.
Shawn Buckley · 7:00:41
And to stop wasting their— meaning the medical system's— time.
Julie Woods · 7:00:46
Correct.
Shawn Buckley · 7:00:48
On two other times, they'd say things like, you're incompetent and you're stupid.
Julie Woods · 7:00:55
Correct.
Shawn Buckley · 7:00:56
So here you are experiencing, um, what anyone would, would describe as debilitating symptoms, and you're basically being abused. I, I don't know what other term to use.
Julie Woods · 7:01:10
Yeah.
Shawn Buckley · 7:01:10
And, and this is—.
Julie Woods · 7:01:11
These are just examples you're giving us, but yes, those are just examples across the total of 23. Um, my dad, who attended every one of those appointments with me, and myself heard everything in between that.
Shawn Buckley · 7:01:27
You were called a drug addict by a neurologist.
Julie Woods · 7:01:30
I was.
Shawn Buckley · 7:01:33
What, um, like, how does that— how does that affect you when you're suffering terribly and basically you're being ridiculed because they cannot acknowledge that you're vaccine injured?
Julie Woods · 7:01:46
I mean, my family doctor tried to make all the referrals possible, and the majority of people got back to her saying that she needed to refer me to psychiatry because that's all I was, was a psych case. And after hearing that from 23 different people, eventually you start to believe it. And so I thought that maybe they were right. Maybe it was all in my head. And that's when I ended up finding React19 in the United States. And I realized that I wasn't alone and this wasn't all in my head and that other people were experiencing exactly what I was. So I had the opportunity to participate in their pilot emotional support group. And through that was actually when I started to realize that my symptoms were consistent. With small fiber neuropathy and with postural orthostatic tachycardia syndrome.
Julie Woods · 7:02:48
And at that point, I started asking the Canadian specialists to test me and none of them would.
Shawn Buckley · 7:02:55
Yeah. So, so you joined this REACT19, is a group in the United States of COVID-19 vaccine injured persons.
Julie Woods · 7:03:03
Yes.
Shawn Buckley · 7:03:04
And so it's this community where people can share what's happening. They also, you know, look into research and so you can learn about things. So you're Basically learning you're not alone and you're also learning, wait a second, other people that have similar things. This is, this is, these are the diagnoses, but no Canadian specialist will test you.
Julie Woods · 7:03:25
Correct.
Shawn Buckley · 7:03:26
So you have to pay to go to the United States and then they actually say, yes, you have this and you have this.
Julie Woods · 7:03:33
Exactly. So not only was it confirmed that I did have the very conditions that I told Canadian doctors I knew I had with the small fiber neuropathy and the postural orthostatic tachycardia syndrome. They also confirmed that I had mitochondrial dysfunction, insulin resistance, and microclotting.
Dean Allison · 7:03:58
All right, Julie, I'd like to hear a little bit more about CANRISE.