Last week I spoke about WHY, I ride. But I am going to go further here. The crux of having type-1 diabetes is that because it is an “invisible” illness people do not understand it, or fall prey to the … Continue reading
It’s a funny thing, I don’t share this blog with most people. I am a little voice in the greater DOC, but I ask friends to follow or read it. Why? because I am content writing and if someone finds … Continue reading
That right there could be my entire post for the day. It sums me up in one word. Normally I tell people I am indescribable or possibly just fucking weird.
But let’s look at today’s topic.
Lets wrap up the week by sharing a little more about ourselves, beyond the chronic illness we or our loved ones live with. Share an interest, hobby, passion, something that is YOU. If you want to explore how it relates to or helps with diabetes you can. Or let it be a part of you that is completely separate from diabetes, because there is more to life than just diabetes! (This topic is a suggestion from the 2016 #DBlogWeek survey.)
I periodically recycle this pic when I have nothing else to say, so I think it applies to yesterday as well.
This post wasn’t difficult to write, but I was still delayed in it’s writing. Internet went sporadic on Thursday afternoon and it took the better part of a day for company to fix the issue. So anytime we had bandwidth, I was actually working.
There are many ways in which to say who I am. But honestly, I am not the one to say them. This is not a false humility thing. It is a reality of who I am. If you were to ask any person who meets me to describe me, you would get the answer of “Sarcastic” after that, the explanation of who I am varies from person to person, based on our interactions.
If nothing else, I like to think I am normal and calm. But the reality is, I am multiple levels of odd mixed with uniqueness and bizarreness. I am awkward, yet awkwardly funny. I am horrible in groups of people I don’t know, that is really where the awkward escapes and embarrasses me. I am a weird friend with quirks.
Honestly, that is a touch of who I am. I am a cyclist, a hiker, and ultimate frisbee player. I am a gamer, a reader, and a pro napper.
I am many things. Each of these things makes me, me. The one thing my friends do not lump into their descriptions of me, is a person with type-1 diabetes. They know, but it is not who I am. Yes, over the years type-1 has shaped me, but the reality is, I do not let it define me. So, I do not let my friends use it to define me either. It is a part of who I am. But I never let it rule me or anything like that.
So this is me in a nutshell and me going off to get some waffles.
Weird topic header right?? I’ll get to that in a second. Today’s writing prompt is great. So much so, I did it on Tuesday. However, here it is again.
Today let’s revisit a prompt from 2014 – May is Mental Health Month so now seems like a great time to explore the emotional side of living with, or caring for someone with, diabetes. What things can make dealing with diabetes an emotional issue for you and / or your loved one, and how do you cope?
Anyway, I am veering slightly again. First off, sorry it took me so long to start today’s post my internet went down earlier today and this is the best I’ve had in over 6 hours. Plus earlier, I was recovering from a low. Anyway on to my title.
I figured I would wildcard it today. Since I am PERFECT, I have no bloopers to share. Instead I will talk about waffles.
Channeling my inner Genie from Aladdin, this is no ordinary post on waffles. It does have a valid point, which I will get to in a second.
I always have Eggo waffles on hand, they are an all purpose food. In fact because I was too lazy to go food shopping for the past week, I have had waffle lunches, dinners, breakfasts, snacks. And it is so good.
But here is why I love waffles, they work for you on so many levels. Think about it each waffle is 13.5g or a serving is 27g. Let’s say you are low, mind you yes you need to wait for them to cook, but you make a waffle, put some jelly on it, and now you have roughly 20g of carbs in your system, both fast acting from the jelly/jam and the “longer” acting carbs from the actual waffle. I feel it’s a good balance.
They are consistent in size, shape, taste, etc. But things get even better if you want, think about it. Let’s say you need to get something in as a snack before bed, you put peanut butter on it and now you have something that will last longer in your system if you are worried about anything happening at night.
They are the perfect delivery food for whatever you need, plus at least for me they taste damn good, hell I even eat them plain.
If you are still with me, obviously this is my own opinion and my own obvious WILDCARD, but the reality is, we all have that comfort food that is something we can eat consistently and get the results we need, which takes some of the stress off of everything else. When we talk about our own mental health we need those gimmes, while obviously this is not a “free food”, it is something I am familiar with. So I singe the joys of my waffles for breakfast, lunch, dinner, bedtime snack, low treatment, or just my reward for making it to Friday.
Have a good day, stay sane. Have a waffle on me.
I don’t like this topic. I am not a fan of this suggestion. It’s a good one, but it’s not me.
Today’s we are told:
Having diabetes often makes a visit to the doctor a dreaded experience, as there is invariably bad news of one kind or another. And sometimes the way the doctor talks to you can leave you feeling like you’re at fault. Or maybe you have a fantastic healthcare team, but have experienced blame and judgement from someone else in your life – friend, loved one, complete stranger. Think about a particularly bad instance, how that person talked to you, the words they used and the conversation you had. Now, the game part. Let’s turn this around. If you could turn that person into a puppet, what would you have them say that would leave you feeling empowered and good about yourself? Let’s help teach people how to support us, rather than blame us!
We all hate the confusion, we all hate the stereotypes, we all hate the misinformation that is out there. I mean even now, with comments in the media that seems to place the blame on the person for getting diabetes. It’s ridiculous.
Yet, I am not going to share a story, I am not going to justify today’s post with a story. There is the ongoing reality out there that people will have to work on diffusing misinformation. But we as a community are not the only ones who face this issue. I mean if I get lung cancer, people will assume it’s because I was a smoker, but the reality is I never smoked a day in my life. People are always going to draw their own conclusions. I think the bigger thing that we as a community need to do, is have that willingness to inform the misinformed. But I think the bigger thing is that we can’t get angry, we can’t get overwhelmed, we can’t let it get us down. There is lot’s of stupid to fight. If maybe today we just can’t, there is always tomorrow.
Honestly, I think this is the bigger issue. Not dwelling on the past, the past is done. Instead work towards ending that stupid.
If you are just finding me for the first time I should warn you, I don’t always follow instructions. More so, I tend to ignore rules and requirements too. I should also add the “sarcasm” disclaimer as well. Once again … Continue reading
(It’s weird starting something in parentheses, but I feel that this pseudo disclaimer needs to be at the beginning of this post. The past few month’s I’ve considered rebranding my blog, but that takes way too much effort for me … Continue reading
Last week, Aug 13 – 16, I wandered out of the great state of confusion and New Jersey to participate in my first JDRF Ride to Cure Diabetes in LaCrosse, Wisconsin. I have done a ride before, but that was … Continue reading