Tag: diagnosis


Jesus, Wheelchairs, and Radiology

15
March

On Saturday, I fell. No big deal, right? I wouldn’t have thought so, except that when I fell, my left foot slammed down on the ground. My toes started bruising almost immediately, as did many other places that didn’t even hit. My mom tried to get me to go to the ER, but I didn’t want to. Going to the ER generally leads to a 3-4 hour wait, a possible trip to radiology (isn’t always a guarantee for me), and then a rude dismissal from the staff (about an hour and a half after being taken to the back–if I even get that far) because I’ve ended up wasting their time.

‘My foot would get better’ was my initial thought.  I fall quite a bit, and usually I’m okay within a few days.  Instead, by Sunday, the bruises and swelling were worse, as was the pain.  I was also having some stiffness in the joints that connect my toes to my foot.  Still, I didn’t go to the hospital.

On Monday morning, I called the UAB Clinic folks so that I could see my family doctor (or another family doctor in the clinic).  Well, I just so happened to call on the day that at least 2 of the doctors who were scheduled had decided to take a sick day.  (I’m sure they didn’t just decide to take a sick day, and that they were actually sick.)  So, they were too busy for the staff they had and couldn’t see me.  Instead of saying that they would see me another day, they told me that I needed to be seen ASAP.  Well, before they could say where I could go, they had to know what insurance I had.  I told them it was Medicare & Medicaid.  Apparently, none of the walk-in clinic are into the whole Medicare-Medicaid combo, so the only other place to go was (cue dramatic music) the ER.

The ER on a Monday is not the best place in the world to be.  It isn’t necessarily the worst, but it’s pretty damn close to the worst place you could be in town.  I went in and, after filling out a form where I put the symptom as “left foot & ankle”, was immediately triaged, which wasn’t necessarily a good thing.  From the first nurse in triage, everyone ignored the foot part of the symptoms and just focused on the ankle.  I thought it was weird that they would do that, though I don’t know why it would surprise me.

After being triaged, I sat in the waiting room for another 3 hours.  I got to people watch, which was fairly entertaining, but not exactly what I wanted to be doing.  There were some interesting people there.  A guy was sitting across the room, under one of the HD televisions, laughing and talking to himself.  My dad and I tried to figure out what to call the guy.  (Please don’t tell me that it is rude to talk about people in a waiting room.  This can sometimes be the only source of fun when you’re in a waiting room.)  We debated between Charlie (for Charles Manson), Jesus (for, well, Jesus Christ), and some others that were related to the guy’s main look–long, wavy-ish dark brown hair, a dark beard, and a look of being in touch with something “else”. We ended up calling him Jesus. My dad thought the guy was probably just crazy.  I thought that he was probably high, but might also have some craziness.  I regretted referring to him as Jesus later, because though I thought that Jesus might wear acid wash jeans and a matching jean jacket, I didn’t think he’d wear sneakers.  (Jesus would definitely wear sandals.)  There was a group of people that we (and a lot of other folks) paid attention to as we waited.  It was a group of about 10-15 people, who, among other things, were very loud.  The security guards chastised them at one point for being so disruptive.  They tried to bum-rush the back to see their friend, who had apparently been beaten up.  Of the five or six people that were part of that rushing past the door when it unlocked for one or two to go back, only two were allowed to stay back there.  Apparently, the ER rule of two visitors per person was lost on the group.  Though this group of people had gotten there at the same time as me, they left about an hour ahead of me.  The only employee that we ended up watching was one of the security guys who’d rolled me into the ER.  He was confiscating any wheelchairs that had been abandoned, even if the person was in the bathroom.  I made sure to hold on to my wheelchair.  (I’ve learned that the staff doesn’t take hurt feet very seriously if you’re not in a wheelchair.)

By the time I was finally allowed to go back to a room, everyone who’d been there before me was already either seen and discharged, seen and waiting on a diagnosis, or had given up on the process and had gone home.  Several of the people who’d come after me ended up being seen before me.

When I got to the back, they kept talking about my ankle, even when I showed them where on my foot I hurt.  I found out that x-rays had been ordered about 2 hours earlier, but that there was a very long wait for the whole hospital to get seen in the radiology department.  (I didn’t understand why they couldn’t send people to one of the other connected facilities [via the tram] that has a radiology department, but apparently that wasn’t a possibility.)  The doctor, who I saw for a grand total of ten seconds, just told me that it was taking forever to get the radiology department’s attention.  A few minutes later, a radiology tech (or someone from transportation) took me down to the department.  I, then, waited for about 10 minutes for someone to wheel me into the room for the x-ray.

The x-ray was done on my ankle, which I was really perturbed by, but I couldn’t get across to anyone that the brunt of the fall had been “absorbed” by my foot.  (I had, by this time, learned that you never give too much information on those little sign-in forms.)  So, after the x-ray was done, I was taken back to my room.  There had been a shift change in nurses while I was in radiology, so I met my nurse at about the same time that the nurse practitioner came in to tell me that my ankle was fine.  My father and I gave him a weird look that should’ve given him a big clue that my ankle wasn’t the part that was really hurt.  (This is why physical exams, which had never taken place, are important in diagnosis.)  He asked what was wrong.  I said that my foot was the problem.  He said that he would check the x-ray again, but the ankle x-ray usually shows the foot.

That is what a standard ankle x-ray shows.  That little area of where the foot meets the lower leg.  That probably hasn’t changed since I first started getting ankle x-rays over 10 years ago.  That kind of view doesn’t show the part of the foot where the toes (phalanges) meet the foot (metatarsals).  It barely shows any part of the metatarsals at all.  It shows the tarsals, aka the ankle.  If an ankle x-ray was the same as a foot x-ray, then there would be no need for calling them different things on forms and there would be no need for different views.

Well, the nurse practitioner, who was sure that the x-ray showed the right part of my foot, was proven right–though, this happened while he was out of the room and with no input from any other medical professional.  I could’ve complained and refused to leave, because I’ve done that before, but it generally ends with the doctor or a supervisor coming in and defending the position of the staff member who made the shoddy call.  (Generally, it is a call made by a doctor who hasn’t been attentive or this particular nurse practitioner–I think he may have been part of the team that made the decision with my mom’s first ankle break to send her home over the weekend, even though she couldn’t bear weight.)

Now, I know that nurse practitioners can do a lot.  And I know that they are generally really good at their jobs, but this guy didn’t do an exam and acted like there wasn’t really anything wrong.  And his end diagnosis?  My foot is bruised and I have a sprained toe.  I’m not exactly sure which toe is sprained, since 3 of them have been in a lot of pain and 1 has been in a bit less pain than those 3.  Only one hasn’t had any kind of pain, bruising, etc.   On the discharge orders, I was told to take Tylenol for the pain, because I guess it works better for pain than Tramadol.  (That was sarcasm.)  I was also told to follow up with a family doctor.  The discharge orders were signed by the same doctor who’d spent 10 seconds talking to me, and was also the same doctor who (on the day my mom had to come back in with the first broken ankle) had written me a prescription for Ibuprofen (can’t take NSAIDs) and spent 10 seconds with me and all of the other poor end-of-the-spectrum pain cases in the same room.  Of course, that day I didn’t get an x-ray, which I kind of feel like I didn’t get yesterday–except that I know that I did get one, even if it was the wrong one.

The Huntsville Hospital ER has really gone to shit.

Comment » | General, How I Met Your Neighbors (aka An Overactive Imagination), Rants, Sickness and Health

Only a Test

20
May

I got back from my neurologist appointment. I didn’t actually get to see the neurologist. Instead, I saw his Nurse Practitioner. She decided that the headaches were probably tension, so I have to take a special muscle relaxant. I also had a bunch of tests scheduled, which she marked as “routine”. Given the number, and the usage for some, that marking was kind of worrisome. Oh, and I found out that I have degenerative arthritis in my lower spine that was confirmed on the MRI from last year.

Blood Tests Ordered

  • ACTHAdrenocorticotropic Hormone – To help diagnose adrenal and pituitary diseases such as Cushing’s syndrome, Cushing’s disease, Addison’s disease, adrenal tumors, and pituitary tumors
  • CBC w. differentialComplete Blood Count -To determine general health status and to screen for and monitor a variety of disorders, such as anemia
  • CMPComprehensive Metabolic Panel – The Comprehensive Metabolic Panel (CMP) is a frequently ordered panel of tests that gives your doctor important information about the current status of your kidneys, liver, and electrolyte and acid/base balance as well as of your blood sugar and blood proteins. Abnormal results, and especially combinations of abnormal results, can indicate a problem that needs to be addressed.
  • Copper Level – To measure the amount of copper in the blood, urine, or liver; to help diagnose and monitor Wilson’s disease; sometimes to identify copper deficiencies and excesses
  • Cortisol – To help diagnose Cushing’s syndrome or Addison’s disease
  • Folate – To help diagnose the cause of anemia or neuropathy (nerve damage); to evaluate nutritional status in some patients; to monitor effectiveness of treatment for B12 or folate deficiency
  • Hemoglobin A-1-C – To monitor a person’s diabetes and to aid in treatment decisions; to screen for and/or diagnose diabetes and prediabetes
  • Homocysteine – To determine if you are folate-deficient or B12-deficient; to help diagnose a rare inherited disorder called homocystinurina; to determine if you are at increased risk of heart attack or stroke
  • Motor/Sensory Neuro Eval
  • Parathyroid – To determine whether PTH levels are responding normally to changes in blood calcium levels; to distinguish the cause of calcium imbalances; to evaluate parathyroid function; during surgery for hyperparathyroidism, to confirm removal of the gland(s) causing the problem
  • Rheumatoid Factor – To help diagnose rheumatoid arthritis (RA) and Sjögren’s syndrome
  • Sed RateSedimentation Rate – To determine the presence of one or more types of conditions, including infections, tumors, inflammation, and those leading to the breakdown or decreased function of tissue or organs (degenerative), and/or to monitor the progress of disease or effect of therapy
  • TSHThyroid Stimulating Hormone – To screen for and help diagnose thyroid disorders; to monitor treatment of hypothyroidism and hyperthyroidism
  • T4, FreeThyroxine – To help evaluate thyroid gland function; to help diagnose hypothyroidism or hyperthyroidism; to screen for hypothyroidism in newborns
  • Vitamin B-6 – To determine B-6 deficiency.
  • Vitamin B-1 – To determine Thiamine deficiency
  • Vitamin B-12 – To help diagnose the cause of anemia or neuropathy (nerve damage); to evaluate nutritional status in some patients; to monitor effectiveness of treatment for B12 or folate deficiency
  • Vitamin D 25 – To determine if you have a vitamin D deficiency; to determine if your vitamin D supplementation level is appropriate, if you are receiving vitamin D therapy
  • ANCAAnti-Neutrophil Cytoplasmic Antibody test – This test is highly specific for certain autoimmune diseases affecting blood vessels (Churg-Strauss Syndrome, Microscopic Polyangiitis and Wegener’s Granulomatosis).
  • SPEPSerum Protein Electrophoresis – To help diagnose and monitor multiple myeloma and a variety of other conditions that affect protein absorption, production, and loss as seen in severe organ disease and altered nutritional states
  • SSA – To help diagnose and distinguish between autoimmune disorders (Sjögren’s)
  • SSB AB – To help diagnose and distinguish between autoimmune disorders (Sjögren’s)
  • Zinc – To help diagnose Zinc deficiency
  • Vitamin E – Deficiency leads to edema, hemolytic anemia.
  • Triglycerides – To assess the risk of developing heart disease

Other tests

  • Nerve Conduction Study – A nerve conduction study (NCS) is a test commonly used to evaluate the function, especially the ability of electrical conduction, of the motor and sensory nerves of the human body.
  • Electromyogram – EMG is used as a diagnostics tool for identifying neuromuscular diseases, assessing low-back pain, kinesiology, and disorders of motor control.

4 comments » | Sickness and Health

Anger Issues?

6
May

I found out a gem of a comment that my (former) psychiatrist wrote in my chart after my first visit with him. Apparently, in that one session where he was supposed to do a quite long and intensive psychiatric evaluation, he spent 5 minutes with me and determined I had anger issues and severe anxiety. Given that I have a pretty good memory of the session, since this was before I was on Risperdal, all I can really recall is me giving a brief rundown of how bad my depressive symptoms were, telling him I needed a better anti-psychotic, and that I was wanting to come off of the Depakote since I had gained so much weight on it. He had put me on Effexor and Risperdal, then told me I could come off the Depakote because I was “on too much medicine”. (I was on the Depakote, Klonopin, Effexor, and Risperdal.) He then sent me on my way, only billing for a med check.

According to my therapist, in the next session he claimed to do a psych evaluation, which is crap because he never spends more than 5 minutes with me. He always tells me I’m on too much medicine. He ignores me when I tell him which symptoms are worse, and tries to get me to up my Klonopin, even though I’ve told him that I can no longer take it because it knocks me out. (Besides that, I don’t feel I need it because I haven’t had a full-blown panic attack in almost a year.)

He also said that I had the symptoms for Borderline Personality Disorder (which I had previously been diagnosed for, but I did not tell him I was experiencing any of the symptoms for it at the time of any of the appointments) and I guess this is his justification for not paying attention to my ACTUAL problems. Ugh. I didn’t really have any anger issues towards him until I found out about him going through my old parts of my chart to come up with his present diagnosis. Hasn’t he ever heard of actually doing the work himself? Yes, it takes a while to do a psych eval, but it was in his schedule and he would have been somewhat compensated for it.

2 comments » | Mental Health, Rants

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