WEBVTT
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Hey everyone.
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Before we dive into today's episode, I have a quick favor to ask.
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Now let's get into today's episode.
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I have yet in, in the hundreds of people that I have worked with chronic pain, I have yet to meet a woman that has not had her pain blamed on her weight or anxiety, whether or not she even has anxiety.
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Imagine battling chronic pain for years, finding your way out against all odds only to be hit with a whole new set of medical challenges that no one seems to understand.
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That's exactly what happened to today's guest, Amy Eicher.
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In this episode, Amy takes us on her journey from being dismissed and misdiagnosed to becoming her own best advocate.
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She shares the hard truth about navigating a healthcare system that often doesn't.
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Listen, I.
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The reality of living with long covid and the surprising lessons she's learned about resilience, pacing, and self-advocacy.
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These stories are too common, but ones healthcare professionals must hear, so we can better honor and respect the expertise that a patient holds.
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Whether you're a clinician, a patient, or someone who just wants to understand the human side of chronic illness.
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This episode is packed with eye-opening insights and practical takeaways.
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Stick around.
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This is one conversation you don't wanna miss now onto the episode.
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This is the Modern Pain Podcast with Mark Kargela.
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Amy let's give people a little bit of an update if we'll link the episode before we, you had a quite the journey with your challenges around SI joint and fusions and really coming out the other side in a much better spot and, challenging maybe the status quo of why you got there and really helping a lot of people with your coaching will definitely get into that, but I'd love if you could update people on what you've been dealing with as of late with some of your new engagement with the healthcare system.
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Sure.
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So in, in brief summary back in 1992, I got hurt as a college athlete, had SI joint problems.
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In 2014, I finally resolved that through a deep dive on pain science.
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And since what, 2018?
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18, I have been coaching other women in chronic pain because I was no longer in pain and I'd learned all this stuff and I had clawed my life back.
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And I thought maybe that would be useful to people after being in the clinic as a PTA.
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I span both sides of the table for anybody that's new to me.
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So in.
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December of 21 my darling partner and I went out to dinner and then went on a road trip down to New Orleans.
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Came home and Christmas Eve my glands were swollen and I was quite certain that I had strep throat.
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Went in, turns out, I had COVID! Ha! Surprise! And I was like, but strep throat.
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And they were like no, no strep throat, definitely COVID.
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And after about 12 days, my heart rate was really elevated.
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I was extraordinarily fatigued and it felt like I couldn't catch my breath.
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And then I think there was probably some pressure on my chest, which my.
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Primary care would later ask me a bunch of questions and be like, yes, Amy, most people would call that chest pain.
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And I was like, Okay, doesn't really feel like pain I've experienced, but sure, we can call it that.
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And he was like, so most people would have gone to the ER.
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And I was like, oh, I don't like the ER.
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They've, they treat me like a drug seeker.
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I don't go to the ER.
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I don't do that.
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So there may be some problems that one occurs after being a chronic pain patient and then actually having medical emergencies and not going
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I'm curious about that.
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Cause you, and we spoke to this a little bit before going on, but like you went into your, this issue around your SI green to the medical systems view on things and especially how you hadn't been exposed to pain science at that point.
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You had went down a road that many patients before you went down and, obviously.
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Took you climbing yourself out, which again is always the interesting thing.
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A lot of the folks in similar situation like Gillette is another one who found their way out on their own, despite health care, let alone with health care.
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So I'm curious when you go into health care, knowing that they're probably not as prepared to deal with.
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the complexity of your situation.
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Not that folks out there aren't trying to help people, but we know that we're not arming healthcare professionals in their graduate education, their entry level education, knowing much about pain.
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I just saw somebody posting, they lectured in a medical program and they were actually shocked.
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it's still a big issue that folks that we encounter in primary care and EDs aren't really well versed on pain.
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I'm curious, knowing that, how it affected your engagement this go around.
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so I go into any new medical professional armed with What I think so first of all, I don't access medical care unless I really can't solve it on my own and I will.
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That's the 1st thing I tell whoever it is, right?
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I am here because I cannot solve this on my own.
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I've been trying for 2 weeks, 3 weeks, 4 months, right?
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I give them the duration.
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I tell them what I've tried in a bullet point list and try to keep it to less than 60 seconds and I rehearse it before I go in.
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So that's where I start.
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And then I, because I do, because I have split the table I come in usually with some things I want ruled out.
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And I will say, I am concerned.
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So what ended up happening was I went back to prompt care.
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They said, you still have COVID.
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And I was like, cool, but we're at like 14 days.
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And my heart rate is like cookie.
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Like I'm laying on my couch and my heart rate is 140 and my O2 stats are dropping to 86.
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And then I feel dumb as a rock because my brain hasn't had enough oxygen.
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Do we maybe want to like, look at that?
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And nobody knows what's going on at this point, right?
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Like long COVID in December of 21 really isn't a thing.
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So there's not a whole lot to look at, other than the fact there is this community that is continuing to experience awfulness after the virus, typical incubation or whatever.
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I complain, they tell me I'm just anxious and they send me home.
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And the minute I hear from any doctor it's just anxiety or it's your weight.
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I know it's time to move on.
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I apologize to interrupt.
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I was actually just about to ask you this because I remember when my wife, I don't know if you remember the episode or if you heard, but she had a microembolic stroke.
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She lost strength in her right side, facial droop, all the whole nine.
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And I remember sitting there in the room and I was ready to reach across strangle some people because they're like, are you sure you're just not having some anxiety?
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The lady's right side is weak for God's sakes.
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I don't think it's her anxiety,
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And I think it's important for our listeners to hear that.
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I have yet in, in the hundreds of people that I have worked with chronic pain, I have yet to meet a woman that has not had her chronic pain blamed on her pain blamed on her weight or anxiety, whether or not she even has anxiety.
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I do now.
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Thanks to y'all y'all.
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No
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Yeah you bet I get in with a new provider and you better believe my blood pressure is higher than it is when I'm with a provider that I know and trust like darn tootin because I go in going, am I even going to be believed?
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So I go to my primary care.
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We're like.
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Sympatico, he gets me, he walked with me through all of the pain stuff, and then has watched me come out of all of that, and we've had great conversations around that.
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So when I said, hey, my heart's doing like really weird things, my normal resting is like in the 50s, and I'm currently in the 120s, 130s, and I don't feel good.
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I feel really bad.
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And it just so happened that while I was in the office and the, I was in the, pre intake or whatever, my heart did its thing.
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And the nurse triaging me was like, Are you okay?
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And I was like, it's fine.
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Now it's when it drops that I start to look all And then it started dropping and she was like, Oh my God, you look like you're going to pass out.
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And I said, it's a good thing.
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I'm sitting then.
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Huh?
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I have inappropriate sinus tack and I had to go through the normal cardiologist who, Let me know that I was overweight and I was like, yeah So this is all happened in the last nine months.
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I gained like 50 pounds in nine months I went and like from fairly normal 40 something year old woman to like completely menopausal like all of my Chick hormones just dropped off and we were like, okay, that's weird.
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Turns out that happened to a lot of women in their 40s after a COVID infection, but we didn't know that yet.
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That research was in process, hadn't been completed yet.
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Got kicked into menopause.
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We put me on HRT, hoping that would help this brain fog and this tired, sluggish Stuff and that didn't work finally got to the electrocardiologist after a five day stay in the hospital, which I can't even tell you about because I will get so angry that let's just say that all of the bad things that every other guest that's experienced stuff has talked about that happened.
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So I'm on the table, they're fishing the thing up through my femoral artery, right?
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I'm awake as can be, the anesthesiologist behind me, we're on a first name basis at this point.
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Because I don't want to feel any of this.
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There's a student with the doctor.
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It gets to about my belly button.
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He's advancing, right?
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And I point and I say, I feel tugging right here.
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Doctor says, you can't possibly feel any tugging.
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Student says, she's pointing right where we're at.
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And I'm like, love you.
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You're going to be in so much trouble.
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Like when you're done here, I basically leaned my head back and said to the anesthesiologist, is it okay if we turn that up some?
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And he was like, yeah, you got it, Amy.
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So he turned me up and then I became much more entertaining until they had to go through the septum of my heart to get what they wanted.
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And then they knocked me out.
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So I was no longer troublesome to them.
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But it was amazing to me that in the procedure while it's happening and they can see it, that they're telling me, no, that's not, you're not feeling what you feel like, what is that?
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Why do we do that?
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What?
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I know you can't answer that, but if your patient is saying something, and I know we're mostly physical therapists here that are listening to this, but if they're telling you something, how about we just believe them?
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I sometimes wonder if it's just it doesn't make sense, right?
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Maybe 99 out of the last 99, but this hundredth patient feels it and it doesn't fit the rule and Therefore, they must be making it up.
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Why don't you say I don't know.
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I think that's just the hard thing for folks.
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And I don't know if it's just a, clutching to your status as a all knowing, expert where I think the X, the best experts I've ever seen are the ones that are willing to say, you know what, I'm not sure why you're feeling it there, but let's figure some things out and see what we can do to make you more comfortable.
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And.
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Instead of invalidating your experience.
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Cause they just they didn't have the answer, that it's because some fancy medical explanation type thing.
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Yeah
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and I forgot how I got to the hospital.
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So I had to have a stress test and climbing the stairs, my heart rate was getting in like 180 to 220.
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I get I'm out of shape, Mark, but I'm not that out of shape, right?
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that's like higher than the highest intensity hit training you can do right there
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And I'm like slowly meandering up the stairs at 180, 220, right?
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As you can imagine, having your heart rate elevated for any amount of time when it's that high makes you a little tired when you're done.
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So we put a halter monitor, which led me to a stress test.
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And then during the stress test, I started throwing out S.
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V.
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T's everywhere and those didn't die down and my blood pressure skyrocketed and my heart rate skyrocketed and everybody in the room freaked out but me because I was like, but this has been happening for four or five months.
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I keep telling you all.
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I'm not scared because I have yet to pass out and nothing terrible's happened.
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I just need to go to sleep and it will go away.
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And they were like, no, you need to go to the ER.
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And I was like, oh, that's way too expensive.
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No, I don't.
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So they let me like stay there for 15 minutes.
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Like three cardiologists came into the room to watch the monitor.
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Everybody but me was flipping out.
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And I was like, I've been telling you all this at every point.
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Isn't it interesting?
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Our integrity is challenged, like that this, it just can't be like when they don't, when people don't fit the textbook, which a lot of our people, as you well know, when person's in pain don't at all.
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So the, just absolutely invalidation that folks go through until.
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apparently the objective proof backs up their experience.
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smacking you in the face and going off as an alarm in the stress test room, right?
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Now, I will say that we are, there's approximately 400, 000, 000 known cases of long COVID worldwide at this point.
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So chances are.
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As a provider for musculoskeletal, whatever, you're going to come in contact with somebody that is experiencing long COVID symptoms and has no idea.
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that is highly likely, so take a cursory course.
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Get yourself acquainted with, the over 200 symptoms.
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That are out there, but like POTS is super real and you had a great podcast on that As is post exertional malaise, and we do not treat that the same way that we treat deconditioning.
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Wanted to, Daria Oller we had on who's got long COVID and long COVID.
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physio is a great resource for folks to, to get into it as your clinician.
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Cause I agree.
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I think Imagine, Amy's journey, your patients are going through the same journey of all these weird symptoms that because we don't have a litany of RCTs to perfectly explain it, healthcare doesn't really have, unfortunately, a great way to deal with it.
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And unfortunately the reaction is invalidation and all the things that you went through.
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Yeah, and then Emily Rich's episode on POTS, huge.
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I'd love if we can, yeah, I'd love if we can get into your post exitional malaise thing.
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Cause I think.
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You know how we are as physios, you're a PTA, and you've been doing this, you're back in the clinic, we'll talk about that.
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Our solution to most things is exercise, right?
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Exercise your way out of it
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Yeah, and then we almost invalidate people and shame them because you're not moving, you're not exercising, yet that is not the best solution for a lot of folks who deal with post exertion release.
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I'm wondering if you could one, speak to your experience of what it's like having it and then how your approach to thinking about exercises may be evolved as a result.
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Yes, so I will tell you once I got my heart results back that said I did not have any inflammation in or around my heart.
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I was like, all right, I just got it.
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I just got to exercise my way out of it because I'm a PTA and I don't know how to do this.
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Wow, is that dumb?
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You don't know what you don't know.
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Until you learn more, right?
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So I started walking thinking it's been, it's been like 6 months at this point.
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They fixed the SVTs.
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They did an ablation and he was also able to find some of the misfiring nodes that were causing my heart rate to skyrocket.
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So he was able to reproduce that by poking at stuff in my heart, burned it.
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And that stopped the astronomical heart rates.
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Like it still is.
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Disequitous and they labeled me with inappropriate sinus tachycardia.
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So it's not like POTS is much more positional.
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Mine just cuz,
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Yeah.
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Just does it regardless of position.
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right?
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So I wish I could lay down to make it better, but I, it doesn't like I can be asleep and it can hit 120 just because any shot of adrenaline will make my heart rate skyrocket.
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So I can't be stressed out.
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Yes,
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your rides at Disney world?
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Like I know, you talked about this.
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Is that something I think you've willingly decided there's things you're willing to expose yourself to in, in the service of your values, which Disney world I know is one of the
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Is one of my values.
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If I could turn my camera, you would see my wall of ears and
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Love it.
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It's next to me, but yes, I decided like the whole family decided we were going to take a trip to Disney and my partner also has long COVID, but he wouldn't call it that.
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He just says he still gets tired at unusual things.
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So we postponed it a year because he and I were both like, I don't think we can do Disney.
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I don't think we're going to survive the experience.
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And I knew from all the pain stuff that like, oftentimes when you're in an environment that you love, when you're doing things that you love, you can do a lot more than you think you can, because I talk about the cup from Greg Lehman I've taken a ton of stuff out of my cup by being in this environment, having it match my values, being with my family, doing all these things.
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So there's a lot more room to make, yeah.
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Harebrained ideas, like walk 12, 000 steps at Disney.
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Did you run up against any people like saying, what the hell are you doing?
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Be it medical or anything to say you shouldn't do that.
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Did you have anybody or
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by that so I got rapidly discharged from the cardiologist because they're like there's nothing else we can do for you lose weight.
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And I was like.
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We're done.
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We're done here.
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We're done here.
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And my primary care, like I cannot imagine Dr.
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Hancock saying that to me basically what we've done for the last four years is I come in with all the inflammation research and stuff.
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And he's on the post viral reserve research stuff.
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And then.
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We talk and I'll say, okay, patients tried this nicotine patch or patients are trying Ozempic or patients are trying low dose naltrexone.
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Here's what the patient community is saying.
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Here's what research says about the inflammation and these things.
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You take all your medical brilliance and tell me if you think that's applicable to me.
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Like we talked hyperbaric chamber at one point and he was like, I don't think that's worth it.
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Like not for you and your symptoms and your presentation, maybe somebody else, right?
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So we just go back and forth with ideas.
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And then it's.
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Are you willing to prescribe to let me try that?
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Or Amy, are you willing to take this?
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And try my suggestion?
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It, I think this is a great example of a doctor that embraces shared expertise, right?