Showing posts with label food. Show all posts
Showing posts with label food. Show all posts

Friday, December 7, 2012

You Can Lead a Horse to Water....

I pride myself on being on top of Maddie's diabetes, for the most part. The only
times I'm not is when things are chaotic, I'm putting out fires, fixing or
cleaning up from a meal, and she runs off to her room. (Another time I'm not on
top of it is when she goes somewhere without me, Shawn or my mom, all the while
PROMISING to check her blood sugar, and correct for it, and for her food.) But
I'd say that 95% of the time, I'm on top of it.

So now that she's 12, and thinks she's 25, our conversations go something like
this:

"Maddie- correct for your blood sugar, and bolus for 60 carbs."

{Silence}

"Maddie! Correct for your blood sugar and 60 carbs!"

"Ok."

{30 seconds go by....}

"Did you correct?"

"I'm getting ready to."

{30 more seconds go by....}

"Did you do it?"

"Mama, I'm really getting ready to!"

"Do it now."

{silence}

"Maddie, I'm waiting...."

"Ok. Correct for my blood sugar and 60 carbs" as she runs up the stairs.

"Don't forget!"

"I won't. I'm doing it now!"

Fast forward 2 hours.

"Maddie, did you correct?"

"Umm...."

"Check your blood sugar NOW!!"

At this point, she is usually very high, and you know how this story ends....

I wonder why I have to ask her to do it so MANY times, (the pump is attached to her body, so she doesn't have to go far to get it,) yet she forgets to correct. I know the years ahead are going to be hard, but I'm not sure I can handle the teenage years AND diabetes. I am trying to instill in her that SHE controls her diabetes and SHE controls her health, therefore SHE controls how she feels throughout the day.  I want her life to be "normal" and I absolutely hate that she has to deal with this stupid disease every hour of the day. 

Friday, September 2, 2011

Starting Over



This past summer, we made a very important decision.  Maddie decided that she wanted to go back to school.  Instead of going to the private school where she attended K-2nd grade, with a full-time nurse to keep a watchful eye on her, she went back to public school.  Back to having 25 kids in one class, back to me not knowing what or how much she's eating, back to a nurse being at the school ONE day per week, back to regular daily recess and PE sessions, and back to me worrying about her for approximately 5 hours of the day.

I honestly enjoyed homeschooling Maddie.  I can't guarantee that I was the best teacher in the world, but we had a really good time.  Unfortunately, I'm not one of these supermoms that I have come in contact with on a weekly basis over the last 2 years who have made it their life's work to educate their children.  I just did what I had to do at the time, and now I'm through with it.  When I started really thinking of all the "normal" fun things that she was going to miss out on by not being in a school setting, I started to feel guilty.  It doesn't have anything to do with her social skills, but more importantly, little things like chatting with her friends at lunch and recess, playing an informal game of kickball on the playground, field trips, Go Far, and the list goes on and on..... 

I had started thinking about checking into the school where the neighborhood kids attend.  I asked around (including people whose kids do not attend there) and found that it was in fact a great school--the best elementary school in the county.  I made a brief mention of "going back to school" to Maddie, and she was all over it.  All it took was one tour of the school, and she was hooked.

Then came the logistics.

"Maddie, you HAVE to remember to check your blood."

"Maddie, you have to speak up when you are feeling low, or are high."

"Maddie, you have to call me if your site needs to be changed."

"Maddie, you have to remember to give yourself insulin when you're through eating lunch."

"Maddie?  Maddie?  Maddie, are you listening to me?!?"

Then it came time to talk to the teachers, principal, and nurse about diabetes.  They are so very sweet.  I laid everything out very simply and neatly, and they took notes, and asked questions, but they have never had a diabetic child at the school before, so I still worry.  I was surprised to find that they were all attending a Type 1 seminar before school started, but I'm not sure how much information they were expected to retain--sometimes things like that are very overwhelming.  I do believe that if there is a question about anything, they will not hesitate to call me.

So, now we've been in school for over a week, and I have to say, she LOVES it.  Every day there's a new friend.  Every day, something hilarious happens in class.  Every day, they do some crazy-fun experiment or game.  Every day is better than the day before.  But still, every day I worry about her blood sugar.  But at least I know she's having a great time and enjoying herself, and that they're taking good care of her....every day. 























Tuesday, March 9, 2010

Reilly

When Maddie was diagnosed, she was almost 6, and being that her birthday is 10 days apart from her little brother's birthday, Reilly was almost 2.  He doesn't remember the wretched summer that she was diagnosed.  He doesn't really understand a lot about diabetes, but he knows that it's a serious thing in our family.

For a long time, he called it "beetees" and he knew that beetees hurt his Sissy, and that we don't like beetees, and that when you have beetees, you have to go to the doctor more times, get more shots, give more blood, and a whole lot of other scary things.

Over time, and after hearing us openly discuss the importance of Maddie's blood sugar, insulin, food, pump, exercise, and overall health, he's come to understand a little bit more about it....well, as much as a 5, almost 6 year old without diabetes can understand.....or so I thought. 

They play a lot together at home, so he has learned to be patient when it comes to waiting for her to check her blood, or waiting for her to give herself her insulin, or waiting while she gets her site changed.  He just knows that it's something that she has to do, and she can resume playing as soon as she's through with whatever it is that she needs to do.

Today, we were riding in the car, and as usual, we were in a rush.  And as any other frazzled mom would do, I drove through the McDonald's drive thru to feed my kids their lunch.  There is one very important thing here that I need to state in my defense.  Upon eating the entire contents of a happy meal, although nutritionally it's horrible for her to eat, I know the exact number of carbs she's putting into her body.

**For the record, I prefer Chick-Fil-A, but unfortunately, it's not on my way home.

Yes, I know that it is not real chicken, and everything is fried, and that essentially it's total crap, but nonetheless, I know the exact number of carbs that she's eating.

As we drove, she and I went through the whole song and dance, which goes a little something like this:

"Maddie, did you check your blood?"

"Yes."

"What were you?"

"127."

"Did you eat all your nuggets?"

"Yes."

"Did you eat all your fries?"

"Yes."

"Even the ones in the bottom of the box?"

"Yes, mama."

Then I tell her to give herself insulin for the correct number of carbs, according to the nutritional labels inside McDonald's, on the Happy Meal box, and on my nifty little iPhone app, in which I know ALL nutritional information of a bazillion food items at a bazillion different restaurants all over the USA.  And fortunately, it's correct every time.  She's never high afterward.....usually..... 

Anyhoo, my point to all of this is that after hearing us discuss this over and over, and after hearing us talk about diabetes at home, at church, at school, and after many explanations, I assumed that her brothers (to an extent) were as familiar with this disease as we are, in an age appropriate way, of course.  Honestly, I guess I had never thought about what they thought diabetes was, or how it "happened".    

The car was quiet, everyone was finishing up their fries and ready to tear open the almost-unopenable toy with their teeth, and I hear a little voice in the back of the car.  It was that of my sweet Reilly, my middle child, my almost-kindergartner, my rough and tough soccer player, and my one who gives some of the best kisses.

"Mama?"

"Yes?"

"I know you love Maddie, and I know you take good care of her, but could you PLEASE not give me beetees when I'm a big kid like her?"

All of a sudden, I realized that he knew NOTHING about diabetes.  Somehow, he thought that Shawn and I had "made" or "let" Maddie have diabetes.  He thought that we had given permission for this to happen to her, and that we may decide to let him or his brother have it, too.   

My heart broke into a thousand little pieces.  I don't even remember the drive home.  I didn't know what to say, or how to respond.  How could he think that I had control over this, and how could he think that I let Maddie have it?  Why would he think that?  Why would he think that I would do that to him?

After I gathered the pieces of myself that had been scattered by the words of a 5 year old, I thought about my response for just a minute.

"Reilly--Daddy and I didn't make Sissy get diabetes, and if I had been given a choice, I would NEVER have let her get it.  If I could, I would give anything in the world for her to NOT have it.  We wouldn't do that to any of our babies--you know that!  For some reason, God has allowed her to have diabetes, but it's okay, because we know that He is in control of it.  We don't know why now, and we'll never know why she has it.  But we are going to trust Him, and take good care of her so she stays healthy.  I don't think God wants you to have diabetes, although if He does someday, we'll know just how to take care of you.  But you know that no matter what, God is going to take care of all of us."

He didn't respond to my reply, and Maddie didn't chime in either.  Brendan, who is almost 3 and doesn't have much to say about anything, was also silent.  We drove the rest of the way home without a word.

I don't think Reilly was asking me that so that he could be selfishly assured that he was in the clear.  I don't even think that he even cared about my long and drawn out answer to his question.  Actually, I don't think anyone was even listening to what I was saying.  Unfortunately for me, that happens often in my family. 

I, however, was listening to the words that were coming out of my mouth.  I don't even think that they came from MY blond head.  I think it was just God's way of reminding me (yet again) that, not me, but He is in control of everything.

 My Reilly

Saturday, September 5, 2009

10 Things I Want My Friends To Know

Here's another good one from www.juvenation.org:

10 Things I Want My Friends To Know

  1. When I'm testing my blood sugar or giving myself insulin, please don't get grossed out or make a big deal about it.
  2. Please stop telling me I can't eat something because there's sugar in it!  I can eat all the same things as you can, just in smaller portions and with a dose of insulin.
  3. Just because I've had diabetes for a long time doesn't mean I'll ever get used to it.  Most days I'm fine, but some days my diabetes can still get the best of me.
  4. I'm not going to die every time I check my blood sugar or experience a low.
  5. You don't need to announce to everyone that I have diabetes.  I'll tell them if I want to.
  6. Having diabetes is like a full-time job and can be exhausting, so please be patient with me.
  7. Just because I have diabetes doesn't mean that I can't play sports and do all the things that everyone else does.
  8. It's OK to ask me questions about my diabetes.  I want to help you understand what it's like.
  9. I didn't do anything to cause my type 1 diabetes, and there's still no cure.
  10. Diabetes doesn't define who I am, it's just something I have.
The funny thing about Maddie and her friends is that a lot of her friends feel like they have to look out for her or protect her from harm.  She really thinks it's sweet.  She loves her friends!!

That Summer

That was a long hard summer. I had a child that I had to give shots to 8 times a day. I had to prick her finger 10 or so times per day. I had to watch what she put in her mouth. I had to make sure she wasn’t shaking from getting too low. I had to check her urine for ketones. I had to check her blood every 2 or 3 hours during the night. I had to tell her she couldn’t have the foods that she was used to eating. I couldn’t let her out of my sight for more than an hour or two. I had a toddler that had already begun to enter the “terrible two’s”. My husband went away for week long trips, 3 times. I had to start preparing Maddie for kindergarten…... Oh yeah, and I unexpectedly got pregnant. Nice…..