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AttituDe of GratituDe inSOULin

Ode to my D-Bag

When this diabetes journey began,

I was embarrassed and kept you discreet,

Keeping you out of sight,

In a purse at my feet.

💖💙💖

Sometimes I’d forget you at home

And regret it while I’m out,

As my blood sugars roamed,

Up, down, and all about.

💙💖💙

I must say I’ve improved,

At taking you everywhere with me,

I’ve even given you a better look,

So you stand out to everybody.

💖💙💖

For holding all my crap,

Oh D-Bag thank you so much,

Holding my pricks, my meter, my insulin…

You know, my pancreas and such.

💙💖💙

Until that awesome time,

When the cure will come our way,

My buddy you will be,

With me each and everyday.

💙💙💙

Want to spread diabetes awareness while donating to diabetes research!? Go to www.teenanigans.com and order some chariteenanigans today! Proceeds from the sale of charity shirts go to JDRF via Team Cut The BS’s OneWalk team!

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AttituDe of GratituDe getting eDucateD inSOULin

10 Reasons Why it Rocks to Hang with a T1D Parent!

I was invited by a T1D mom (that means her child has T1D) for a night out since her amazing daughter with T1D was away at Diabetes Camp. Basically this means that she can have a little break from managing her daughter's diabetes (the camp counselor and nurses assist with that during that week.). I had an amazing time and thought…T1D parents rock and I just had to share or with my Cut The BSers…so here is:

10 reasons why it rocks to hang out with a T1D parent!

1. They're so ready for a night out. Having the opportunity to let your hair down and have fun is rare for a parent of a T1D child…so when it does happen…ya wanna be around!

2. They know what you're doing at the happy hour table. No questions as to what we are doing and why there's blood on my finger.

3. They know how to carb count!!! Since they do all the carb counting for their child…they can do it for you too! Bolus me!

4. They're always in mom/dad mode. Adulting can be hard…adulting with T1D…can be even harder. Sometimes it's a relief to pass the torch on to someone who understands because I won't argue with them they way their T1D child might. Tell me what to do…it's cool! I'm soooooo ok with that!

5. They always have a juice box ready! They also have glucose tabs and other random treats on them. They are always equipped in case of a low!

6. They probably volunteer and are members of the same community you are in. So those days when you can't go on…they're there to remind you to keep going…but not before we enjoy this happy hour!

7. They have a sense of humor about diabetes. Sometimes we have to and they have some of the best stories! I'll drink to that!

8. They don't judge…ever. I've never heard, "Should you be eating that?" from a T1D parent. It could be because they have spent so much time helping their own T1D kid(s) live normal lives and bolusing for normal things that they don't blame us one bit for ordering that elephant ear!

9. We can be a resource for them. We can be here to be sounding boards. They can ask us if we were rebellious at their kid's age and why, or how they can be supportive of their child. They can ask us to describe what a low feels like and how we may need to be helped. It feels good to be able to give back to the people who take care of us.

10. They have the biggest hearts ever! Their hearts are overflowing with concern, advocacy, and love. They are true crusaders to our cause.

Cheers to all the T1D Moms, Dads, Brothers, Sisters, and Friends out there! You inspire me and empower me to continue on this T1D journey. Until our next outing…line dancing perhaps?

Donate to my JDRF One Walk Page by clicking here!

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AttituDe of GratituDe inSOULin

Diabetes Blog Week 2015 Day 1: I Can

Ideas have been floating in my mind about how I was going to start this week’s series of blogs.  This is my first Diabetes Blog Week, and honestly, I’m a little nervous.  How am I going to knock it out of the park?  

I thought about listing all the things I have been able to do since I was diagnosed.  I thought about the fact that after I got home from a week long stay at the hospital, my muscles had weakend and I couldn’t even get up the stairs without crying. And how with determination, I am now able to run up and down those stairs daily.  I thought about talking about my first time eating out at a restaurant with my husband and diabetes and how his encouragement of not being ashamed to check my blood sugars in public and take my insulin in public has given me the strength to be able to do so many other things with him, our girls, and diabetes.  I thought about all the places we have travelled to since then and the people with diabetes I’ve met along the way.  I thought about talking about my JDRF walk team #teamcuttheBS and how much we’ve raised together and how proud I am of the work we’ve done. 

Today’s post is meant to talk about something that I am proud of accomplishing.  And as proud as I am of all these things, nothing beats the text, email, or private message from one of my friends online who has been struggling with the notion of even checking his/her blood sugars.  When I get that message from someone after they see a post of my meter that reads 238mg/dl asking me how I responded or the message that says, “I checked mine today too!”  Or “I found my meter, I can start checking again.”  Or the beer someone bought me because she was no longer “pre-diabetic.”  I’d say those are the accomplishments I find most dear.  

Why? Because until I sat in a room where everyone else checked their blood sugars, every time I checked my blood sugar, I felt alone.  I find it impossible that I am the only person to feel this way.  Why did I feel alone? No one else had to do it, no one else really had to react at the number that comes up (unless it’s super low and I’m passed out on the floor,) and no one else around feels the guilt I do when the number is “out of range” high or low. Loneliness sucks and I wish it on no one.

If I can help someone to find the strength in themselves, to get out that effing meter, prick themselves and brave whatever number flashes on that screen, then I have it it me to do anything.