Showing posts with label malingering. Show all posts
Showing posts with label malingering. Show all posts

Sunday, January 25, 2015

Episode 52: Down the Rabbit Hole: Will I Finally Get a Diagnosis for My Breathing Difficulties?


Worshipping air again, tonight. Holy, sacred, life-bestowing air. Never take it for granted. Yes, I've written on this very topic with some of the very same evidence before, but lack of air tends to become an all-pervasive problem. Air, sports fans, is kind of important.

Photo by Lisa Sheirer
Used with permission

Today I had a horrendous deep, barking coughing fit after I laughed real hard at something Honey said, and I've been coughing and barking since.

I'm wondering now whether this might be the clue that finally makes my pulmonologist believe me when I say how quickly I run out of breath when merely taking a walk or walking up a flight of stairs.

As I've said again and again, this is the most frustrating part of being a patient. My pulmonologist doesn't believe me when I tell him about these symptoms.

Why do I think this?

First, he ordered a six-minute walk test. As the two of us walked, I told the technician that my oxygen saturation would probably be just fine when we stopped at the end of six minutes, but if we waited a minute or two, it would drop. I knew this based on my own observations about the effect of exercise on my ability to breathe.

"That's not how the test works," the tech told me. She measured my saturation just after the six minutes, and it registered 100 percent, and that was the end of it.  After that I sat down and clipped on my own oximeter, and within a couple of minutes, my saturation had dropped to 82 percent. But no one cared about that.

That's not how the test works.

Well, guess what? That's how my lungs DON'T work, and that's why I'm in that office spending medical dollars so I might have some kind of a chance for a life if this thing can be treated.

Fast forward to next visit. I again tell the doc about these symptoms.  Sports fans, these are the very first symptoms that started my recent fall down the rabbit hole of today's health care system. They became debilitating during a trip to Europe during Christmas 2012-New Year's 2013.  I had absolutely zero stamina on that trip for stairs, for walking, for doing anything at all.

It's now a full two years later, and while I've been diagnosed with quite a few things since them--cardiomyopathy, sleep apnea, idiopathic hypersomnolence, kidney disease, and degenerative brain/muscular disease--I think that's it--no one has yet explained this lack of oxygen on the slightest exertion. This isn't just fatigue, which would be expected given all my diagnoses.  This is a very specific reaction to exercise or, to be more accurate, exertion, since even brushing my hair can wear me out.

The first time it happened was well over a decade ago, when my sister and I tackled Mt. Baldy, a mountain in California near our aunt's retirement home.  We took a ski lift up most of the way and were supposed to then take an easy trek across the ridge to the apex at 10,000 feet. We had started at sea level, since we were close to the Pacific Ocean at the base of the mountain, so that's a pretty fast elevation change.

My sister is seven years older than I, and she was trucking along, but my body stopped itself flat and told me, "You ain't taking another step, Girlfriend."  I had to stop numerous times, and starting up again was pure hell.  I finally made it to the apex, but I knew what I'd experienced made no sense, given my then-young age and seemingly good health.

The problem now is that it's happening without shooting up to 10,000 feet in an hour or two.  I also have a history that includes coughing up blood resulting in a bronchitis diagnosis, a bout of pneumonia, and a diagnosis of reactive airway disease a few years ago. And, as I've said a thousand times, there's that damned polycythemia that still shows up in all my lab tests, and the most basic cause for that is a lack of oxygen in the system.

So, back to my trusty medical librarian skills--maybe this severe cough after laughing,which has been happening to me for some time now, will indicate the cause of the problem.

And I think, perhaps, I've found it:  exercise-induced bronchoconstriction. In other words, after exerting oneself, a patient with this problem has trouble breathing because the bronchial tubes, the same culprits in bronchitis, narrow to a potentially dangerous degree. The problem is common in asthma sufferers, but it can also occur in people without any history of asthma.

And laughter, it turns out, affects those bronchii the same way--it is considered a trigger as strong as exercise.

For more on this condition, read about it in this 2011 article from American Family Physician.

I just pray that when I see Dr. P, as I'll call him, this coming Wednesday, this new observation will make him take me seriously.  But I think I may have already told him about this symptom, as I told you, Dear Viewer, in an earlier blog.  I had a major coughing fit while watching a silly scene in an Ace Ventura flick, and that ended with my coughing up about a cup of phlegm. Dr. P. didn't seem to care about that, either. 

During my last appointment, I told Dr. P what had happened with the six-minute test, so he told me to get up and follow him.  He then had me walk up a short flight of stairs in his office building and clipped an oximeter on my finger. His tech again took the measurement and, as I could have told them, of course--no decrease in oxygen saturation.

Well, no duh!  The office building was as cold as ice, and I"ve noticed that heat makes the problem much, much worse. Not only that, I'd just gone to the office after a night on my CPAP--the appointment was first thing in the morning. My symptoms aren't constant, but they are frequent.  And they get worse as the day goes on. The more I do, the worse they get.  It's a cumulative thing.

I tried to explain that to Dr. P, who told me, "If it doesn't happen here in the office, it doesn't happen at all."

I understand doctors need objective evidence. But if a patient consistently complains about a symptom, doing one or two tests that reveal nothing should not be the end of it.  In reading about this condition, I learned that recommended tests include spirometry with and without exertion.  I've had it without exertion twice, but never have I been given that lung test with or after exertion.

And, one of the characteristics of exercise-induced bronchoconstriction is that it happens during or after exertion. So why does the protocol for a six-minute walking test have the oxygen saturation taken ONLY immediately after the end of the six minutes?  What about those of us whose oxygen depletes shortly after that?

"Typical symptoms of EIB include wheezing, shortness of breath, dyspnea, cough, or chest tightness during or after exercise. These symptoms usually occur during strenuous exercise and peak about five to 10 minutes after exercise," state Krafczyk and Asplund in the aforementioned article.

So why would a six-minute walking test NOT check for lack of oxygen for several minutes after the walking ends?

Honestly, I don't frickin' understand what a person has to do to get adequate diagnosis and treatment in this Rabbit Hole known as the U.S. Health Care System.

The cardiologist overseeing my last cardiac stress test told me my heart had performed just fine, "but something is going on with your oxygen." By the end of the test, I was hanging on for dear life; my legs felt as if they were going to give out from under me.

Legs can't run without air.

But nothing about my oxygen, or lack thereof, appeared on the doctor's report of the stress test because, of course, the test was all about my heart function. Well, hello, the two are utterly connected, so why is this?

Even my new physician, whom I'd had high hopes for, told me when I expressed this problem--and that fact that my own oximeter, which my ENT had told me to get when my oxygen was low in his office, drops into the 80th percentile on mild exertion:  "Maybe your oximeter is broken."

I want to scream.  I want to fricking scream.

Maybe there's nothing the doctors can do for my breathing problem, but the frustration of their not taking me seriously and not investigating the problem properly so they and I can know why this is happening to me is driving me absolutely crazy.

I had almost made up my mind that I wouldn't even bother mentioning this problem again this time. It's so discouraging to be made to feel as if I'm making the shit up. But now with this horrendous coughing, I have something else to bring to him. And he'd better take it seriously this time, or I might have to do something desperate. Like write an article and send it to the local paper about the frustration of my quest and the lack of care I'm getting. Don't want to do that. Just want my doctor to do what he's supposed to do.

Remember how excited I was when I was going to see the neuromuscular specialist at Hopkins, who I'd hoped would take my neuro symptoms seriously and give me a DNA test for myotonic dystrophy?  Remember how utterly disinterested and cold she was to me that day, and how disappointing that encounter ended up?

I fear that will happen again this Wednesday.  Going to the doctor shouldn't have to feel like you're about to enter into a battle, but that's exactly how it feels.

"Patients with atypical exertional complaints require careful clinical and physiologic evaluation," says American Journal of Respiratory and Critical Care Medicine authors McFadden and Zawadski.

So why haven't my complaints been carefully evaluated?

A couple of aspects of EID that don't exactly match my situation are that it normally occurs with strenuous exercise, and I haven't been able to do strenuous exercise for a long time. It also occurs tends to occur with "physically active" persons, notably athletes, and I haven't been physically active, much less an athlete, in quite a long time. I've had to give up hiking and bicycle riding. Hell, I've had to give up walking. I've had to give up evenings out with my friends. I've had to give up sex, on a far too frequent basis. I've given up showering and grooming most days. I've given up cooking for myself most days. Every frickin' thing I do exhausts me and leaves me out of breath.

Have I used the word "frickin'" enough times yet? Hey, I'm mad. I'm trying to keep it clean, though.

Certainly I was being physically active when climbing Mt. Baldy those 15 or so years ago. And I first noticed the severity of my symptoms while forced to be physically active during my trip to Europe in 2012, since I had to walk a lot and use stairs in buildings with no elevators. Now, my problems occur with the mildest of exertions, but perhaps that's because the condition has progressed (or regressed) to this debilitating state.

Another problem with the diagnosis is that cold air is known to induce an attack. I, on the other hand, find that hot weather brings on my breathing difficulties much more than cold weather does; however, I do not spend much time in cold weather and certainly don't exercise during cold weather, so I can't really say whether this would affect my breathing or not. The brief trip up the short flight of stairs in the air-conditioning at Dr. P's office wouldn't have induced anything because of the brevity of the test--it was a silly, non-test in my view.

Yes, I'd said that I get out of breath when climbing stairs, but I was talking about the steep, long flight of stairs in the Victorian-era building in which I'd worked at the time. The little flight of wide steps Dr. P tested me on was no comparison.

Krafczyk and Asplund also note that "Self-reported symptoms have been shown to be poor predictors of EIB because other conditions, such as vocal cord dysfunction, can cause similar symptoms. Therefore, symptoms alone should not be used to diagnose EIB."

Okay. I buy that. So give me the right damned test to figure out what the hell is going on--especially since the symptoms can be treated. I would dearly like to do a few things without having to give up in exhaustion because I can't breathe. I'm tired of waiting around for the doctors to believe me enough to give me the right tests.

Let's hope this time, this Wednesday's appointment, things go a little better, and answers are forthcoming. That's all I want. Frickin' answers. What else are my medical dollars paying for? It's like a bad student's being passed from grade to grade. I'm a patient being passed from appointment to appointment. Problem student, problem patient--What's the strategy? Give up on them! Teachers and doctors who do that don't deserve the salaries they draw, in my humble opinion.

I don't want to have to dread my doctor's appointment, but that's exactly what I feel. Dread. And yet I want those answers, so go I will, and do battle I will, if necessary. My quality of life, and my very life, depend on it.

Meanwhile, we just had a snowstorm, and it's bitter cold out. Maybe I'll do a little six-minute walk tomorrow and record the results with my oximeter, taking a photo of those results. Sounds like a good idea to me. But will Dr. P buy it, even then? Most likely he'll just think it's another example of my "obsession" with my health.

Damn straight, I'm obsessed. Anyone would be, if he or she could not breathe properly and could not do much of anything, anywhere, any time. It's miserable.

And I'm damned sick of it all--being sick and exhausted and out of breath and stuck in the U.S. health care system of today, the Rabbit Hole where nothing makes sense. The Rabbit Hole I find myself in today. The Rabbit Hole whose passageways are constricting, tightening, and burying me alive.

___________________

REFERENCES

Krafczyk, Michael A., and Chad A. Asplund. 2011. "Exercise-Induced Bronchoconstriction: Diagnosis and Management." American Family Physician 84(4):427-434.

Parsons, J.P., et al. 2012. "An Official American Thoracic Society Clinical Practice Guideline: Exercise-induced Bronchoconstriction." American Thoracic Society Documents: 1016-1027.







Friday, August 29, 2014

Episode 44: How Can a 54-Year-Old Woman This Damned Sick Look This Damned Good?

Okay, I'm taking all of us on a little Mary Dell ego trip today.

Actually, I started this episode a year ago, when Honey also took the photo I'd planned to accompany it. I'm a year older but don't look much worse than I did then. I've moved the photo to the second page of this episode to save virgin eyes from seeing it if they don't want to. Hey, it's not pornographic--just a bit suggestive.

Yes, come with me .... hop on my magic carpet ride to a land where the marvelous science of photography (without any tricks such as PhotoShop) suggests that I may not be so darned hideous after all--certainly not too bad for a gal of my advanced (50+) years. You see, my entire life, I've always felt unattractive--or, at least, the core of me did. I could fake being attractive and convince men I was attractive, but I never felt it deep inside.

And now, ironically--how many ironies does chronic disease rack up? (pun intended)--Answer: A LOT--the attractiveness that others see is doing me a disservice (though I'm happy to have it regardless).

The fact that I don't look like a middle-aged, chronically ill woman means that many health professionals I see once or twice think I'm malingering or trying to get attention or some other stupid shit, and they don't take me seriously. For the latest egregious example of this phenomenon, see Episode 41 and my nightmare consultation with a neurologist at Johns Hopkins Medical Center.

The fact that I don't look like a middle-aged, chronically ill woman means that co-workers, friends, even my sister and one of my sons, neither of whom sees me nearly enough, have hinted at finding my complaints hypochondriac in nature. With my son, I'm thinking it's sort of denial--no one wants a sick mom. With my sister, I think it's just that I'm the youngest and can't possibly know what I'm talking about, ha.

But I love them both dearly, of course, no matter what. None of this is easy to take in, even as I experience it day by day.

Hopefully, given the latest neuromuscular diagnosis, signs, and symptoms, those who know me well no longer doubt me. One thing my mom pounded into my head during the 29 years I was blessed to have her in my life was honesty. And the last thing I want to do is waste medical dollars when so many others need care.

And this pic is TAME compared to all the sexting going on, so no big deal there, Mom!

No, I don't look sick.

In fact, I look damned good.

So how can a woman who looks this damned good really be this damned sick?

Wednesday, August 6, 2014

Episode 41: Down the Rabbit Hole and There are Nazis Down Here!

Readers of fiction will recognize the allusion to Watership Down in this episode's title. Watership Down, a popular book when I was in high school, is based on a completely absurd construct: A warren of bunny rabbits must fight to save its society from nasty Nazi rabbits. Believe it or not, it's a terrific read. It works. Which is more than I can say for the rabbit hole I currently find myself in.

In fact, this rabbit hole suffices as a metaphor for the utter irrationality in today's health care system. I've actually encountered Alice's Red Queen; I don't want to call her a Nazi, exactly. Or mix my allegories. Just couldn't resist the literary tie-in.

Okay, okay, enough with the figurative language.  Here's what happened, Dear Viewers, when I finally underwent the long-awaited neuromuscular examination for possible myotonic dystrophy at Johns Hopkins Medical Center. Now, to date, I've been more than pleased with my care at Hopkins, but this experience has likely destroyed my loyalty to said institution.

They'll be happy to be well rid of me anyway. Who am I but one patient, powerless against the juggernaut of Big Medicine, Inc.? One patient jacking up their costs (and their profits) with her smorgasbord of chronic disease. And now that I have Medicaid instead of Blue Cross Blue Shield, I'm doubly unimportant to the system created (but not maintained) to help me and you.

I'm a shareholder liability, that's all I am. "Let them die then, and decrease the surplus population!" Okay, okay, not yet another literary character entering this story, but I often quote Ebeneezer Scrooge at moments like this.

2010-Red-queen
"Off with your head!" says Dr. Red Queen, in so many words. "And no DNA test for you--you've overstepped yourself so I don't care to relieve your mind with an easy yes-or-no answer to an at least somewhat possible reason for your years of suffering and confusion at the ways your health has failed you! So there!"

That's her reflex hammer in her hand, and she refuses to admit the medical sign it renders in her patient, lest her patient be right about something she has no business knowing about! Off with her head, and no DNA test for her . . . NEXT! I have a paycheck to collect and a lifestyle to protect and a reputation that trumps yours, so nyiehaya!
Despite this latest horrific experience (and there have been plenty more than this and the one with my son, believe it or not, in my tumble Down the Rabbit Hole), the Hopkins visit was not a complete waste.

The electromyography (EMG)--a rather uncomfortable test in which a doctor sticks needles into your muscles and records the electrical reactions--indeed revealed some myotonic abnormalities. Thus, although Dr. RQ, as I'll call her, refuses to consider my experience as valid, the machine doesn't lie. This is not over yet.

My true purpose in telling my story is that I want you, Dear Viewer, to understand how the medical system is against YOU, the patient, and how LITTLE YOU MATTER in any quest to learn what is wrong with you or a loved one. Obviously, this needs to change. 

The medical system exists to serve US--YOU and ME, the patients. We, the People. But as this diagnostic nightmare continues to demonstrate, we count very, very little in the stories of our own lives, if we believe what our doctors and other health professionals, insurers, and governments (federal, state, local) tell us. 

But we don't have to believe them. We know our bodies; we can read; we can think; we have friends and family who want to know what is wrong; we have only this one life to live, and we deserve to know what is wrong when there is something wrong. That's what the system is for, but the system too frequently fails us.


Thursday, November 24, 2011

Episode 12: Blood Sludge for Turkey Day

I’m still getting the hang of this polycythemia thing.

You see, my blood is too thick. Too many red blood cells. That makes my blood turn to sludge, and sludgy blood is not good. Not only does it put me at higher risk of heart attack, stroke, and pulmonary embolism, it makes me feel as if I’m full of sludgy blood, which means every cell in my body feels heavy and slow and, well, sludgy.

You’d think that feeling would be easy to recognize. The thing is, it’s insidious. I start feeling bad and, because I’ve had fatigue problems for the past few years, I just accept it, even as it gets worse than usual. And then I finally realize, “Oh, yeah, I’ve got that thick blood thing, too … maybe it’s time to get drained.”