And You People WORK In The Emergency Room?

Early on when I was starting insulin I had some learning curves in the area of low blood sugars (hypoglycemia). I’d been given the diabetic teaching about what to do, and I’d been an RN for 22 years by the time I started on insulin.  Generally, I did well at home getting my blood sugars back up with regular soda or glucose tablets/gel.  One day, nothing was working. I had to call 911 when I hit 37mg/dl, and couldn’t get it to go up no matter what I did.

The paramedics got there, and I was still in the upper 30s.  They gave me more gel, and got an IV going in the ambulance.  I was still conscious and able to talk to them, but I felt BAD. They  radioed ahead that I was coming, and unfortunately I had to go to the closest ER which was notoriously horrible. En route, they gave me an amp of IV dextrose (D50). I had my purse with me that had my backup glucose meter and change for the vending machines. That proved to be incredibly important.

I was given another amp of D50 , and my blood sugar went up to 128mg/dl.  The nurse  (who rarely made eye contact, and just muttered as if I were the most ridiculous thing she’d seen come through the door all day) said she’d called a cab for me; they’d be there in 45 minutes.  I knew that I had to have some source of protein and/or fat to keep my blood sugar from tanking again. The basic information for hypoglycemia says that a snack is needed if the next meal is more than 30  minutes away.  Evidently the EMERGENCY room people didn’t know that basic information.  Straight glucose will spike and then drop. That’s just how it works.  I was sent to the lobby to wait.

Within about 10 minutes, I could feel my blood sugar drop.  I checked it, and it was in the 70s. I got a Coke and some Starburst candy from the vending machines. It wasn’t helping. I got some peanuts to help my blood sugar stay put.  The peanuts didn’t help.  My blood sugar was in the 50s by then.  I went to the triage desk and told them what was going on. I was told I’d already been seen, and a nurse might be able to get out and check on me in a while. Really?  I’d been brought in by ambulance for hypoglycemia, I was bottoming out again, and I was thrown to the whim of some nurse who might get to me?  I was safer in the cab.

I managed to stay in the 50s until the cab got there, and got home where I could work on evening out my blood sugar on my own.  The ER obviously wasn’t going to complete the process with protein/fat sources.  I got some peanut butter, and that helped.  Now when I go anywhere I take glucose tablets or gel and portable peanut butter.  I make sure my blood sugar is in a range that lets me function before I eat the peanut butter, or it will slow down the glucose’s ability to work. The duration of action of D50 is dependent on the degree of hypoglycemia (and the symptoms of low blood sugar are different for everyone at different levels of hypoglycemia).  One person can be unconscious at 40 mg/dl, while someone else can be talking at 30 mg/dl…both are in severe hypoglycemia and need immediate treatment.

I learned a lesson about the emergency personnel’s lack of comprehension on how fully to deal with hypoglycemia.  I have to take care of myself even IN the emergency department at a hospital. At least the shoddy one.  I can’t depend on anyone to help me; I have to be prepared and advocate for myself.

Published by JillinoisRN

A disabled RN who is still trying to find ways to help people. I've got a lot of interests, and a lot of things I'd like to convey to people.... whether they want to 'hear' them remains to be seen :)

6 thoughts on “And You People WORK In The Emergency Room?

      1. 🙂 There seems to be no common ground. You are either amazing at what you do, or you’re so terrible that you shouldn’t be doing it in the first place. Medical apathy is one of my biggest pet peeves. I’ve had two clients die because of one doctor that brushed them off and wouldn’t run the proper tests. Thank god that you can actually advocate for yourself and I’m glad that you actually do.

  1. I’m so sorry about your clients’ deaths, and the lack of care they got. I had to learn to speak up, and now I’m not shy about it since I’ve had so many horrible incidents at that one hospital (I had to go there w/insurance for a while- now I’ve got more choices with Medicare on disability). Some people just go into nursing because of the mythical shortage – a solid profession with a lot of openings; it’s not a job that people should go into for any other reason than a desire to help people. Yes, job security/availability is important- but without some sort of compassion, it shows like mustard stain on a wedding dress….

  2. It is so frustrating to know more about treating your own illness than “professionals” do, isn’t it? :-/ I’ve been there with my eating disorder, unfortunately.
    I’m glad you were able to get through that okay… I shudder to think of how a lesser educated/prepared individual would have fared in your shoes.
    I am only just learning to advocate for myself, “be a squeaky wheel” until I get what I know I need. I’ve always thought of it as “being a pain in the butt”… so I tried to be quiet and small and not inconvenience anybody. A huge part of my recovery has been learning that it is not an inconvenience, it is their JOB, and I have the right to speak up for myself. 🙂 It seems you have that lesson down!

    1. With strange disorders (I’ve got one in particular), I don’t mind it as much, but diabetes is pretty standard stuff. At least I’d expect them to say they don’t know- I can respect that- I can’t respect just proceeding and being clueless. That pisses me off !!

      Continue to squeak ! A big part of eating disorder recovery is feeling worth the care/needs you require. I used to be very shy when I first started nursing school- Lord have mercy ! But I had to get with the program, or I didn’t do a good job. Now, I’m the one I have to take care of !

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