First a little housekeeping… if you didn’t check out the awesome blogs in yesterday’s post, you totally should. They’re called the Best of ‘Betes Blogs for a reason! You can start nominating for November now! (Well technically you could start four days ago.)
A lucky reader has been selected for my NatureBox giveaway! Check your email for a message from me to see if you won! If you didn’t win, don’t sweat it! You can still use the code SNACKTIME for half off your first box and I’m giving away something cool next week sometime.
I was contacted by the American Recall Center and asked to share one thing that I want people to know about living with diabetes.
Everyone with diabetes has a different story, different treatment and there is no one-size fits all approach to diabetes treatment. Even with just Type 1, there are different types of insulin, some people use injections, some people use pumps and even then our meters, pumps and other equipment vary. We have different targets and have different insulin needs. For example, at breakfast I need 1 unit of insulin for every 9 grams of carbs that I eat (which is different from lunch, which is different from dinner for me) and another blogger with type 1 needs 1 unit of insulin for every 20 grams of carbs she eats.
So back to my contribution… I couldn’t pick just one thing and I couldn’t narrow it down to one sentence, so I gave them several thoughts and let them do the editing based on their other input. They made an excellent selection by using:
Diabetes has to be a factor in every decision I make.
I am more than my diabetes but I was diagnosed with type 1 diabetes at 22 and I live with it 24/7, I don’t get a vacation and I have to consider diabetes when in everything from what and when I eat, when I sleep, when and how much I exercise, whether I’m going to get behind the wheel of a car… everything. (yes even what you’re probably wondering about)
I’m pretty open about living with diabetes, I talk about it occasionally and blog about it a lot. Because of that I think that sometimes people forget that I’m Rachel, a wife, daughter, sister, aunt, professional, etc. as well as a person with diabetes. I have a life that diabetes fits into, not diabetes that my life has to fit into. Even though diabetes is a factor in every decision, I’m more than my diabetes. When I was diagnosed, I didn’t stop being Rachel. I also didn’t stop liking chocolate or coffee.
One of the other things I was thinking when I responded is that what I wish people in general knew about diabetes is that they don’t know everything about diabetes. Diabetes varies so much from patient to patient and there are so many types (Type 1 like me, LADA or Type 1.5, Type 2, Gestational, etc.) that knowing about one person’s diabetes doesn’t mean they know about everyone who has diabetes. What works and doesn’t work in the way of medications, exercise, diet and treatment plans for a person with diabetes varies for everyone. It drives me crazy when people think they know what I should and shouldn’t do or eat with diabetes and try to give me a plate of fruit for dessert instead of what everyone else is having. (If you’ve read my blog for very long, you probably know that it really bugs me to be denied the same food everyone else if having… and that it’s happened to me on multiple occasions.)
It’s not right to expect someone without a connection to diabetes to know it all, but having at least a little knowledge and giving up the myths of diabetes important.
Check out what the other bloggers said here.