Letter To A Diabetic

Or I Understand What You're Going Through

Diabetes is a Unique Disease

I found this video on the differences in diabetes from person to person. Worth a watch. Our disease is unique to each of us. We can’t all be lumped into the category of diabetics and treated the same for management.

 

 

And Now It’s Time For A Diabetic Laugh…

I found this on facebook and had to share it here for those of you who have not seen it. I think jokes about diabetes are funny as long as the person telling them actually understands diabetes. Clearly this person gets it.

Copied from this website.

 

29 Things Only a Person with Diabetes Would Understand

Written by Lizmari Collazo

1. Every paper cut is an opportunity to test your blood sugar.

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2. You have an entire drawer, dresser, or closet devoted to diabetes supplies.

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3. You have hundreds of lancets and only a few test strips. But on the plus side, your health insurance company is willing to pay for more lancets!

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4. When it’s time to test, all you have to do is squeeze your finger.

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5. The phrase “once in a blue moon” is a reminder that it’s time to change your lancet.

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6. You hesitate to wear white in case you prick your finger and hit a ‘gusher.’

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7. Your fingers appear to spell something in braille.

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8. Being high means something completely different to you than it does to most people.

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9. You can calculate the carbohydrate total of every meal in your head without breaking a sweat.

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10. You should test your blood sugar six times a day, but insurance only approved you for one strip a week.

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11. You can put a mathematician to shame: insulin on board, carb factors, insulin to carb ratio, no problem!

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12. Well-meaning friends have offered you every diabetes remedy under the sun, from cinnamon to birdseed milk.

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13. You’ve heard, “But you don’t look like a diabetic!”

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14. You’re familiar with all the diabetes horror stories of the relatives of anyone you’ve ever met.

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15. You’ve heard, “You can’t eat that!” too many times.

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16. Everyone wants to know where you got your cool pager.

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17. You find used test strips in your refrigerator but don’t know how they got there.

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18. You have a pile of diabetes cookbooks holding up your sofa.

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19. You own 15 glucose meters, but you only use one.

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20. CSI would have a very hard time ‘investigating the scene’ at your house.

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21. You have two cases of juice boxes at home, and none of them are for your kids.

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22. You have to remind yourself that it isn’t polite to punch people who say ‘diabeetus’ in the face.

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23. The pharmacy is number one on your speed dial, and you’re on a first name basis with the pharmacist.

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24. People often say “You can eat it, it’s sugar free!” about something that’s loaded with carbohydrates.

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25. Everyone asks you what to do about their ‘noncompliant’ diabetic spouse.

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26. You read every article that promises ways to improve your glucose level, but they all end up being about prevention instead.

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27. According to TV commercials, it’s a good thing you’re young, because only old people get diabetes.

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28. There’s never been any butter in your refrigerator’s butter compartment — it’s used for storing insulin.

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29. To lick or to wipe? That is the question.

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“If You Meet Someone With Type 1 Diabetes, This Is What You Should Know” by Justine Nancarrow

A friend shared this article and I think it is well worth sharing here. 

 

Happy Diagnostiversary!

Today is the third anniversary of my diabetes diagnosis. Every year I celebrate being alive and, so far, without any major complications. It’s a big deal, this diagnostiversary. It’s one more year of seeing, one more year free of kidney damage, one more year of avoiding neuropathy. One more year that diabetes didn’t get me. One more year of life. I’m grateful for every day that I can get up, play with my pups, and go through the day with a comfy sofa and wagging tails to go home to. Life is a wonderful thing, and I love mine, diabetes and all. I wouldn’t ask for a different one if I could.

 

Quinoa Chickpea & Avocado Summer Salad

msteck:

Quinoa is a fantastic complete protein. It goes with everything and this recipe looks particularly delicious! Curious about quinoa? Check out some info here.

Originally posted on The Recipe to Life :

Hey everyone! I know it’s been quite a while since I’ve written anything. A natural disaster hit close to home, and I’ve been helping facilitate donations and assistance for families in need, and have not had any time for anything else for quite a while. BUT, on a happier note, things are starting to get organized enough to where I’m able to have some personal time again, and do the things I need to do. Well, ok, not that blogging is something I NEED to do, but I sure do enjoy it. It’s one of those healthy release things I think. So here I am, and I’d like to share a fantastic recipe I’ve found with you. I made it this week and it is wonderful. We had unseasonably warm temperatures in our area this week (Seattle area, try almost 90 at the beginning of May! Holy smokes!), and it…

View original 328 more words

Misdiagnosed

I found this story on the Greater Good website and it’s worth reading. I was originally misdiagnosed (or rather, not even diagnosed). In February of 2011, I went to see an Endocrinologist. I had never been to one but I thought it would help since I believed that the trouble I was having was related to hypothyroidism and I was concerned that my primary physician wasn’t catching some stuff that a specialist would. I was constantly fatigued, depressed, thirsty, had to pee all the time. Right.

So I get to the this doc, whose name I’ll not mention, and this old bloke tells me that he has “seen this before” and what I really needed was to go out and get a career and a husband. Um, can we say jacka**?! He then told me in a condescending sort of way that he would pursue this with me if I wanted. I went home, frustrated, exhausted, and having to pee…again.

August 11th, 2011 I was in the ER. Diabetes. Diagnosed T2 only to realize later it was actually T1 (LADA). So, I know this happens and it probably happens more than we hear about since I suspect there are some serious malpractice implications that go along with these stories. But, whether caught early or late, here we all are, and here’s “Thirteen Years and Counting.

 

CGM (Continuous Glucose Monitor)

After having too many low readings (30s – 50s) with no symptoms until feeling like I was going to pass out, I caved and got the Dexcom G4 continuous glucose monitor. I wish I would have gotten this thing earlier. It’s an awesome device. It spits out a bgl reading every five minutes. It’s user friendly, easy to insert, very small, and gives information on trending. Alarms can be set for highs and lows and I have been told there is an android app that allows users to get info off the monitor from great distances (think kids at school and such) though I haven’t verified this. It is tubeless, and comes in pink, blue, and black. Seriously folks, any T1 who has trouble keeping their bg where they want it should have one of these. Check out the Dexcom page about the CGM.

I have been in bed sick this week and normally in this situation keeping my bg in range is a futile endeavor but I have mostly been able to keep it in the 100s because I have known exactly what it is and where it is going. The information you get on trending with this monitor is invaluable. So take a look, and if you already have a CGM, share your thoughts on which devices and features you prefer.

 

Insulin Pen Approved for Diabetic Dogs

Well looky what I found! A new insulin pen has been approved for use with diabetic dogs. Check the caveat at the bottom – dogs allergic to pork products should NOT use this.

I scanned this straight out of the most current issue of Dog Fancy magazine.

dog insulin pen

Show Me Your Pump!

After indulging in a little social media griping about people’s reactions to my insulin pump in public, someone shared this wonderful article with me. Enjoy!

Hey, Miss Idaho, Is That An Insulin Pump On Your Bikini?

Miss Idaho Sierra Sandison, shown here in her home town of Twin Falls, Idaho, decided not to hide the insulin pump she wears to treat Type 1 diabetes during the pageant.

Endo-Anxiety (or A Rare Condition Involving Irrational Fear of Not Having Control of Your Diabetes).

Another endo visit awaits me on Thursday, during which I will no doubt be weighed and measured, quite literally. Sometimes the trips drive me crazy, sometimes they’re welcome, but they are always useful. And that’s the part we need to remember. You can learn a lot about controlling your diabetes during your endo visit. Remember, though, that you are your only real health advocate and it is up to you to go fishing for information. So next time that (perhaps dreaded) visit roles around, do yourself a favor or two.

~Get a copy of your most recent lab results. After all, that’s why you’re there, to go over results and check in. So get a hard copy and start a file so that you can keep your own records and follow along.

~Let your endo, (and medical assistants) know what you need help with. You’re literally standing in a great resource for information and help. Ask for it.

~Don’t blame yourself if your results aren’t where you want them to be. If you’re alive, and have a good to terrific quality of life, diabetes isn’t winning. Take comfort in that and keep on truckin’.

~But mostly, remember that at the end of the day, you’re head will be on your pillow. Nothing lasts forever, and most of what we worry about is in our imaginations. We worry about things that might happen or will happen or won’t ever happen at all. You’re here, on the right side of the earth for living, and we can’t forget that while we carry a disease around inside our bodies, days come and go, life moves along, and we are just as entitled to living it as anyone else is.

Love and light,

Melissa

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