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We found 10 result(s) that match your search "daily living":

I am going to begin this, my very first blog post here, with a confession.
I have fallen off the wagon.
Not the booze wagon; even before my type 2 diagnosis in February 2006, my drinky drink days were mostly behind me. (College was fun, from what I remember.) No, the wagon I have fallen off of is the healthy living, weight-losing, diabetic-under-control wagon.
When I was diagnosed last year, my a1c was hovering above 10, and I was about 35 pounds overweight. I was also terrified. I was 38 years old, with that big number (let's call it "thirty-ten") lurking in the near future. My own father died at the age of fifty-one after about twenty years of poorly managed diabetes. I was determined that this wouldn't be me. (READ MORE)

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I received a comment on my post from yesterday that really struck a chord with me. The reader commented that their parents had died from diabetes and that they would die from it too.

 

When I read that I got choked up because honestly, I feel the same way.

 

Sure I plan on fighting the fight and checking my blood as often as I am supposed to. Of course I will continue to work on my A1C and losing weight. I am not giving up on life at all. But, in the back of my mind I “know” that diabetes is going to win in the end.

 

Will it be heart disease, kidney failure, or a stroke? Maybe something else. Who knows?

 

The fact is that with all the steps I take to live healthy the odds are against me. Diabetes has the upper hand which makes me sad and angry at the same time.

 

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Last week, I spent several days in Mexico on vacation and on a business trip. With the extra carbs and the change in normal routine, my averages went from the 140's to the high 150's. I had one or two severe lows and a handful of minor lows. I also had one day where my pump site went sour and sent me soaring into the 300's for several hours.

 

Coming back from Mexico has been interesting on my blood sugars. I've had a few lows, of course. But at the same time, I've decided not to try so hard to keep my numbers down. I'm not completely blowing it, but I'm just not stressing myself out over highs and off numbers.

 

So Monday night, I decided to order a pizza while working on a research paper. It was nice to eat the pizza, do a fairly normal bolus, but not stress about what my blood sugar might be in the next 12 hours. I didn't even freak out when I saw consistent 200's on my meter screen.

 

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I want to be the Little Mermaid. I want my ocean life to turn to land. I want to suddenly be able to cross to the other side. I want a day without diabetes. Just one day.
If I could imagine a day without diabetes... it would be hard to know where to start. Maybe I'd go jogging and not worry about getting low hours later. Maybe I would make my day on a holiday so I could eat anything I wanted without thinking about boluses and temp basals.
Certainly I would rejoice in not being glued to an insulin pump and infusion set. I would get rid of the calluses on my fingers from the eight finger sticks a day. I wouldn't worry about heightened risks for heart disease, glaucoma, or even the common cold. (READ MORE)

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Tick, tock, tick, tock.

 

Every one of us with diabetes hears that clock ticking away.

 

Glucose, insulin, ketones, tests.
The endless cycle never rests.
Fail once to heed the daily strife
And that day you may lose your life.

 

Alarmists are everywhere. Family, friends, strangers, all with the best of intentions.

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Every day, I live my life with diabetes the same way. I test my blood sugar, I treat lows and I change infusion sets. It is a part of me. Sometimes, it is all of me. I get frustrated on a regular basis with the highs and lows or the way it interrupts my entire life from school to dating to sleep.
It amazes me though when I look back on all those days. It makes me smile. As frustrated as I get and all the tears I cry, I don't remember diabetes as my past. Surely, it's there. I just don't remember the daily parts of the disease. (READ MORE)

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One underlying theme of diabetes blogs and complaints is the difference of our daily routines from those of people who have never known a blood glucose test, never chosen foods based on specific ingredients or an organization's endorsement, never had to dress in a manner different from those around them, and never had to follow a ritual not of the mainstream. Yet we see, meet with, and talk to people who do this on a daily basis, who could never think of not doing this (or who would never consider it)... who do not have diabetes, nor are they housemates of people with diabetes. (READ MORE)

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It's soft like velvet, it's sweet and buttery and melty, it's just a touch crisp on the outside, and salty. And after dipping a Wetzel's Pretzel into cream cheese I feel as if I've died and gone to heaven.

 

OK, not really, but Wetzel's Pretzels are one of those foods that I hate to love. I crave bread and have since forever. I also crave textures. Yes, really. There are times when I want something smooth like yogurt, or something thin like water, or something heavy like ice cream. So yeah, I crave textures.

 

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People with diabetes, and those touched by diabetes, follow their journey with the disease through a myriad of winding emotional paths. Depression is very common for those newly diagnosed, sadness can rear its head at different stages in the game, and a little humor and humility can even find the door to expose itself from time to time. The keys for controlling those doors are littered all over the place and on  Wrld Diabetes Day today, you can follow this map of internet hotspots. Expose diabetes for all that it is, good and bad, and then share it with others. Find an emotion and embrace it!

 

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On dLife's Facebook page, the following question is posed:

 

There is no doubt that doctors are key to success in maintaining your diabetes. However, not all doctors have diabetes. There are some things that even doctors do not know or understand about living with diabetes. What are some of the things you wish your doctors knew about diabetes and the daily task of living with the illness?

The responses range from issues of doctors not spending enough time with PWDs, giving incorrect information, doctors believing the information we gather about our diabetes is solely for their use (and not ours!), and having poor bedside (or examination room) manners.

 

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