Ever wonder if you should tell people at your workplace about your diabetes? Especially when it comes to low blood sugars and what could happen if you aren’t able to treat a low yourself? Well, that’s the issue we tackle today in our weekly advice column
, Ask D’Mine!
As per usual, veteran type 1, diabetes author and educator Wil Dubois has some tips.
{Got your own questions? Email us at AskDMine@diabetesmine.com}
Hannah, type 1 from New York, writes: I am 29 and was diagnosed with type 1 at age 12. My older brother was also a type 1 and died from a hypo when he was 16, just after I was diagnosed. Fortunately, I don’t have hypo-unawareness like he did, but as a young adult on her own I have been a bit careless about carrying a glucagon kit (I haven’t had one since my freshman year at university). My symptoms for hypos seem to be changing, though, and I know it’s the right thing to get a kit and train my roommates to use it. I’m debating with myself about getting one for the office and training a couple of my coworkers to test my sugar and use the kit. Part of me feels like this is awkward and unnecessary, and the other part feels I owe it to my mom, who already lost one child to type 1, to at least play it safe. Am I weird for even thinking of it? How do people generally deal with their D at work?
Wil@Ask D’Mine answers: Hannah, if you were going skydiving, would you accept the reserve chute? Or would you say, “No thank you. The main chute almost always works.”
Would you book a cruise on an “unsinkable” ship that didn’t have lifeboats? An Artic cruise?
Handle a pit viper without some anti-venom handy?
Diabetes is a dangerous business. As dangerous as parachuting over iceberg-infested waters with a pocket full of pit vipers and no lifeboat. OK… That metaphor really didn’t come together as well as I had hoped, but I guess I made my point. Of course you didn’t really need me to teach you that; sadly, your brother already taught you that lesson.
Stand by while I go light a blue candle for him…
OK, I’m back, and I have some pretty strong feelings about glucagon. Regardless of how intense your symptoms of low blood sugar might normally be, they can change over time, and no two hypos are created equal. And of course, even when we know we are low, sometimes reversing that situation is harder than at other times. Glucagon is our break-the-glass-in-case-of-emergency medication, and none of us are emergency-proof. glucagon, quite literally, can be the difference between life and death.
I’m glad you’re planning to get your roommates on board. And I’d bet they’ll be even more relieved to know how to help you than you
will be to have them know. What I mean by that is that there’s nothing worse in the world than being powerless. Your roommates, on some level, already know that you’re a potential ticking time bomb. Now if something “bad” happens they can take direct action to help save your life, rather than just dial 911 and pray for you while they wait for the ambulance.
Everyone in my house knows how to use the kits. Well, more correctly, all of the humans who live under my roof know how to use them. Training the cat didn’t work out so well. Hypo dogs we got, glucagon cats are going to take some work.
The day after my son Rio turned 5, I sat down and had a conversation with him about glucagon. “Now that you are a man…” And I trained him how to use it. When the kits expire, we use them to run practice drills. He’s dying to use one on me. FYI, I talked a little bit about how and why they work here and here, so today we can focus on the how-to-enlist-other-folks-to-help-you issue.
As to your officemates, I might not have the most objective perspective in the world, as everyone at my office job knows I have diabetes, we have a gazillion BGL meters, dozens of glucagon kits, and the vast majority of my coworkers know how to use them. Of course, I run the diabetes education and treatment program for a FQHC clinic—not exactly the “typical” office environment.
How do non-clinical people deal with their diabetes at work? It’s as variable as flu viruses. Some PWDs hide their diabetes. Some are low-key about it. Some are open about it. Some flaunt it. Readers, I invite you to chime in today via comments on how you deal with your D at work.
Now, I don’t know what kind of work you do, Hannah, or what your office politics are, but I think someone there needs to be “in the know.” It could be a close co-worker; or maybe a reliable co-worker that you don’t even like. It might be a supervisor. Or the janitor. It really doesn’t matter. But you need someone on your team at work, because diabetes really is a team sport. And really, two someones would be better, just for in case your primary someone is out to lunch or on vacation when the Hypo Reaper pays you a visit.
How do you breach the conversation? Well, as a way of starting this rather awkward conversation, you could just print out this column and hand it to the person in question.
Or maybe just this part of it:
Or you can just memorize the lines above and say it to the person directly.
Now, your Lifeguard doesn’t need to know a damn thing about medicine to use a glucagon kit. Actually, that’s sort of the point. Who wants a fire alarm that only a fireman can pull? There’s a lot that ”laymen” can do to help each other, health-wise. That’s why we have CPR. That’s why we have AEDs (defibrillators). Do you know how many lives have been saved with citizen-operated public AEDs? About 1,000 a year. If there were more out in the field, some estimates say that 50,000 heart-attack deaths could be prevented every year.
But back to glucagon. Nowadays most states have programs for training non-medical school personnel on how to use glucagon for type 1 kiddos, although it was a long fight against school nurses to make it happen. Here’s a training outline from California, another from Utah, and another from New York. I think that pretty much gets us from sea to shining sea. You can glance these over for ideas, but don’t let the length of the documents freak you out. Giving a glucagon shot isn’t rocket science. It only takes about 90 seconds to mix the water with the powder inside the vial and draw it back out into the syringe before injecting.
But probably the easiest way to prep your Lifeguard is to simply have them watch a 2-minute YouTube video showing how to use a glucagon kit.
Novo Nordisk makes an inert “training” version of their glucagon kit, called HypoKit® Test Medium. It’s not the real deal, but it comes in a white box instead of an orange one so you don’t get the two confused, and the training kit even comes with an injection pillow for practice. You can call Novo and beg them to send you one, or your doc can request one for free here. Lilly also has a glucagon app available for free on iTunes to use as a training tool for anyone who might need to administer the fast-acting glucose boost in an emergency. Both are great ways for your Glucagon Lifeguard to get some hands-on experience.
Of course, once you get someone—or several someones—on your side, everyone needs to be on the same page about where the
glucagon kit is going to live at your office. Again, I’ve got it easy at work. There’s one in our ER, one at the nurses’ station, one in the lab, several in our pharmacy, and one in my office velcroed to the wall right above the fire extinguisher.
What? Oh. No, those aren’t all for my benefit. We have a lot of D-folks in the building on any given day. Do you need yours velcroed to the wall? Why not? Or it can be in your desk drawer. Or in the desk drawer of your Lifeguard. Unless those desk drawers are as messy and cluttered as mine are, in which case stick with sticking it to the wall. But it really doesn’t matter where it is, so long as it can be found quickly. It should also be near wherever it is that you spend most of your time in the office. Oh. Right. And you should also have a kit at home and one in your purse or Go-Bag.
So do I think you’re being weird for thinking about this? Not even. Not at all. I think you’re being responsible. Responsible both to yourself and to those who love you.
And you’re right: your mother has already given enough to this damn disease. Get yourself a Lifeguard.
Disclaimer: This is not a medical advice column. We are PWDs freely and openly sharing the wisdom of our collected experiences — our been-there-done-that knowledge from the trenches. But we are not MDs, RNs, NPs, PAs, CDEs, or partridges in pear trees. Bottom line: we are only a small part of your total prescription. You still need the professional advice, treatment, and care of a licensed medical professional.


Ugh. Using CPR as an example of what laymen can do to help medically is a BAD example. Just listen to Radiolab’s “The Bitter End” and you’ll find that CPR as a treatment is horribly ineffective from PROFESSIONALS, much less laymen.
Generally speaking, is the internet the cheapest place to procure pens? Do you know if there are programs to help low income diabetics afford these pens?
I had a low blood sugar at work and a co-worker called 911. Yes, I had glucagon in my desk drawer and everyone knows it’s there and how to use it. The cue to my co-worker was that I passed by my own office indicating to her that I was confused. One of co-workers asked me if I was mad that she called 911. No and like the co-worker who called 911..how do you know at times just how fast you are going down. Better safe than sorry.
I’m married to a T1 (luckily we work at the same office) – but imho the scariest thing about *not* telling/training work colleagues is the risk that they’ve seen too many crappy tv shows. You know the ones – the PWD has slipped into a hypo and there’s major panic to find and inject insulin *facepalm*. So if you do have a nasty hypo, in their misguided attempt to help they’ll quite literally kill you with kindness.
Oh, and it will also help them understand that if you are acting like you’re drunk, and/or being surly and belligerant, or downright mean – it’s not because you hit the pub at lunchtime, or that you’re being an a-hole. Chances are it can be fixed by a handful of jellybeans
Not sure if this applies to all countries, but companies of a certain size over here (I think it’s more then 20 people at work at one location) are required to have a certain number of staff trained to deal with emergencies. This includes very basic medical training and I explained my situation, symptoms and remedies to them.
My direct co-workers also knew I was diabetic and the basic symptoms. It has gone wrong only once, but in a major way (my levels were not going upwards even with glucagon and I had blacked out). As I was working in high security building at the time (air locks, biometric scans, the whole lot) this was literally a nightmare scenario.
Everything went off without a hitch however, they had me in an ambulance in amazing time and contacted family, etc. I am still terrified of this scenario happening again (glucagon not being enough, completely blacking out) but if it happens at work, I couldn’t be in better hands. Basicly they had a basic script for if something like this happened and adapated it for diabetes crash based on the information I provided them.
I don’t think talking about Diabetes should be awkward, every coworker of mine I’ve talked to about it, knew other people who also had Diabetes. They often felt however, that it would be awkward for them to start a conversation about it as they were aware it is a very personal thing. I think that getting the ball rolling is in the hands of the diabetic.
In addition, and I think this important, my direct coworker told me she was so glad she knew what to do when it happened. Sure, it is incredibly awkward to have the talk “what happens when I go crazy and/or collapse on the workfloor”, but its nothing compared to the shitstorm that happens when you do go crazy and/or collapse on the workfloor and nobody knows whats going on or what to do. Sure, it has happened once in the 8 years I have type 1 diabetes, but without my coworkers it could have been the last time it happened and everyone is very pleased that wasn’t how it went.
I’ve had T1 for about 6 years, and while I’ve had some nasty lows, I’ve never had a blackout/seizure experience. However, I am on the committee that was sponsoring an educational conference. One of the attendees had a seizure due to hypoglycemia, but NO ONE had any idea what the hell was happening (whether she had a hypo or epilepsy or something else) because she had nothing on her person or in her purse explaining the issue. If we had found a glucagon kit, I would have gladly administered it. It was absolutely terrifying and disheartening to not be able to help her! I have since reviewed how I act when I get low (and what to do) with all of the people who are around me at work and at play, and it doesn’t offend me in the least to have someone ask me if I’m okay.
There are products in development to make glucagon pens like EpiPen (e.g. GlucaPen) which would be much easier to use.
You would think the insulin companies would jump on the chance to develop one of these products, but that doesn’t seem to be the case – they seem to think that these user-unfriendly kits with exposed needles are OK in the 21st Century.
Wake up Sanofi, Novo, Lilly ! – your insulins may cause less hypoglycemia than this competitor or that one, but ALL your insulin products do cause hypoglycemia, and you should step up to this reality by providing a user-friendly product to the patients whose use of your produces is both life-saving, but also dangerous!
I haven’t had a hypo that I was unable to handle yet, but I was diagnosed as T1 only a little over a year ago. I started letting people at work know right away, just in case. It’s no big deal in the workplace; I take my PDM to lunch so I can bolus and carry a tube of glucose tabs to meetings along with my CGM receiver.
But I don’t have a glucagon kit; my doctor has never mentioned it to me. I guess I should get a scrip for one to keep at home in case my husband needs to use it on me and another for the office – I work with nurses and doctors so there are many people around who would be able to handle it.
This disease sure requires lot of equipment.
Unfortunately, that Glucagon app is available in the US iTunes Store ONLY. I’m in The Netherlands, and the Glucagon app is NOT available in the Dutch iTunes Store. I guess Lilly thinks none of us Europeans can read English (or need Glucagon education)
I have always worked with at least one other person in my ‘team’ or physically nearby who was also a PWD. We connect, talk about lows, and help each other out in the workforce. At times, we use each others equipment to test or even shoot up. It’s comforting in a weird way…