10 Reasons Being Insulin Dependent Totally Sucks

10 Reasons Being Insulin Dependent Totally Sucks

When it comes to being dependent on insulin, people always think the biggest problem is needles, but that is just not true. It is easy enough to get used to the pricks, pokes and jabs – although yes, of course it hurts, to those who always ask that question. But really, it’s the least of our problems. There are many other things that not only annoy the heck out of us, but also scare us and cause considerable stress. So, we have compiled a list of ten other reasons why needing to take insulin via injection or pump is not fun.

 

1. Too much can kill us

When taking insulin, it is crucial to get the dosage right, not only to stay healthy, but also because too much insulin can kill us. The hormone that people with perfectly functioning pancreases produce is a life-saver, but when you have to inject it yourself and guesstimate how much of it you need at any given time, it’s got the potential to be deadly, too. We have to put this stuff into our bodies every day, on our own, without medical support or advice, and we do a pretty darn good job of it. But, boy, is it stressful!

 

2. Too little can kill us

I repeat, we must get the dosage right. The unrelenting pressure to constantly ensure you do not have too much, but just enough, insulin in your body sometimes feels like walking a tightrope. Without enough insulin in the body, a person with diabetes may go into diabetic ketoacidosis which can lead to painful complications, coma, and even death.

 

3. We always smell like Band-aids

Insulin smells weird. Those of us who manually put it into our bodies every day know exactly what I’m talking about. It’s that smell that reminds you of Band-aids, a hospital, or a Sharpie marker, and it kind of follows you everywhere. After 25 years living with type 1 diabetes I’ve mostly gotten used to the smell, but I’m always self-conscious that others can smell it.

 

4. A refrigerator is essential

Insulin needs to be kept at a stable temperature or else it can spoil or become less effective. It’s recommended to store insulin between 36-46 degrees Fahrenheit or 2-8 degrees Celcius. This can make travel a nightmare if you’re struggling to find a way to keep your insulin cool. Imagine the stress of having your life depend on something that spoils, and always having to keep it safe.

 

5. We never get a break

Acting as a 24 hour, seven days a week pancreas is both physically and emotionally exhausting. When dealing with insulin, you can’t just think about how much you need each day, but you also have to think about physical activity, food, and all the other factors that impact blood sugar levels. If we stop thinking about these things for any extended period of time, we put ourselves in danger.

 

6. It’s exhausting

If your blood sugar is too high or too low, it makes you tired. No matter how hard we try to get our insulin doses right, it’s impossible to always have perfect blood sugar levels. This means we are regularly exhausted by the physical impacts of having even slightly too much or too little insulin on board.

 

7. Disasters are extra dangerous

Many people with diabetes need insulin every single day, multiple times a day, to survive. So if a disaster strikes, or there’s an emergency situation with limited access to diabetes supplies, people who are insulin dependent are some of the most vulnerable. I often think about what would happen if I found myself in a disaster, like Hurricane Harvey, and it is incredibly frightening.

 

8. It costs too much

Needing a medicine in order to survive means having to pay for it, however much it costs. Even if the cost of insulin depletes our bank accounts and stresses us out beyond belief, we have to find a way to pay it. If that doesn’t make you hate using insulin, I don’t know what will.

 

9. We are often offered unsolicited advice

In best-case scenarios, someone’s ignorance shines through when they tell us that we should just “eat less sugar” so we won’t have to inject insulin. In worst- case scenarios, someone accuses us of “shooting up drugs” when they see a needle. Having to stay calm while someone tries to “educate” us about insulin and diabetes can feel like torture. 

 

10. It’s unpredictable

Remember when I said we have to manage our insulin and food intake 24 hours a day, 7 days a week? No matter how hard we try to get it right, sometimes insulin affects our body in ways we don’t expect. We have no choice but to keep trying, day in and day out, even though we know sometimes insulin will do whatever the heck it wants inside our bodies.

 

Elizabeth Pfiester
Elizabeth Pfiester

Elizabeth Pfiester has lived with Type 1 diabetes for over 20 years. Early on, she found her passions of education and humanitarian work, which took her to the London, where she received a Master’s degree in International Development and Humanitarian Emergencies at the London School of Economics and Political Science. Elizabeth started www.t1international.com last year to create a space to easily navigate global diabetes resources, organizations, and existing literature about care, policy, and treatment in places where Type 1 diabetics are often forgotten. Since its inception, she has been conducting interviews and writing articles; she now has readers from over 80 countries.

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Thax Bimly
Thax Bimly
4 years ago

i got T1D at 30. Now 69. on the pump the past year. it did settle the question of god.
there is none. lower case only. when my partner moved out of the bedroom and stopped loving me, that was one of many
self-hating moments. there is no support: nobody hangs around a complainer. and i believe i’m being punished for some reason. i can pretend i’m happy for brief spells, but it’s not maintainable. a string of affairs always destructing. nobody can understand without being a T1. and i wouldn’t wish this hell on anybody….

Loser T1D
Loser T1D
3 years ago
Reply to  Thax Bimly

10 months of the pump was enough. It’s awful. Finding a new site every 3 days eventually fails. Basal failure and your bG 310 in 2.5 hours. A bad joke. The pump is a fraud. Oh God …please go to hell.

Who cares
Who cares
4 years ago

Xmas day 2019
I spend plenty of time hating my T1D-self.
And some time not hating.
If there really is God, then I hate him/her for giving me T1D. Second choice: there can’t be God, because having T1D proves there is no God. Tough choice. The loss of having some one stop loving me, I directly blame on T1D. Spending so much time compartmentalizing excuses and trying to cure loneliness and self hate means no progress. Pathetic. Loser. Maybe tomorrow will be better…..

Ceecee
Ceecee
5 years ago

I hate being Diabetic. I always say it is a life sentence. I am always tired and I get so much more tired from having to worry about what I eat, how much medicine to give myself and having to always check my blood sugar. I’ve been Diabetic for 32 years and it never gets better. It’s a constant struggle.

Eva
Eva
6 years ago

Please…all this blessing stuff makes me gag…Diabetes is not a blessing…that we live with medical technology and tx is a blessing. I hate poking myself 3x day and giving myself shots all the time. I would just like to go to lunch with friends and not have to worry…go barefoot and not have to worry…tired of rotating injection sites, the list goes on…my life is a blessing but not the diabetes.

Leon Malnik
Leon Malnik
6 years ago

I see that there are some angry comments about the statements diabetes is a blessing in disguise. I for one embrace that attitude. Since 1963 I have had to fight the ravashing affects of Diabetes and I am the better for it! It has made me who I am today, a strong independent person wanting to face lifes’ challenges. You can choose to turn your back on diabetes from time to time but diabetes never turns its back on you. That will make us stronger or we die period. I played ice hockey till age 60. I only stopped after… Read more »

maureen Kutcher
maureen Kutcher
6 years ago

I would like to add a number 11. Explaining. Every time you go out to some place to eat. You have to explain, and explain how type 1 is different than type 2. You also have to listen to all the new diet fads that can cure your type 1 diabetes. Julia, I do not believe there are 10 reasons why type 1 is a BLESSING IN DISGUISE. What? Like: 1) You are not dead- you have insulin? 2) Your drugs in Canada are covered by most drug plans? 3) You have to cut down on carbs and maybe loose… Read more »

Glen W. Cameron, C.E.T.
Glen W. Cameron, C.E.T.
6 years ago

I also find that meal time is stressful because often, by the time I get to eat, the food is cold or at best, warm. Others don’t realize the testing of the blood is to be 30 minutes before eating, then the taking of the insulin is around 5-15 minutes before you eat. I hate it when there is no notice at all and all you get is “dinners ready”.

Julia Kostic
Julia Kostic
6 years ago

It’s nice to have people to vent to, but I hope you follow this up with a “10 reasons type 1 is a blessing in disguise.” If course it sucks, and we shouldn’t be irrationality Pollyanna, but what should we focus on?

Shannon
Shannon
6 years ago
Reply to  Julia Kostic

I can not come up with 1 reason for Type 1 Diabetes is a blessing in disguise??? Type 2 possibly only because it may lead you to a healthier life, but 1…nope never!!!

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