Wednesday, December 29, 2010

One disease to rule it all

I am a huge Lord of the Rings fan. I love the interwoven themes, the cast of characters, the rich and deep storytelling. It's a world that you can delve deep and get lost in. Like most of the great tales, I can usually find myself identifying with one of the characters.

Lately I've been feeling a lot like Frodo. The quiet hobbit who was thrust, very reluctantly, into a position he didn't want, and worse, felt unprepared for. He was given a daunting, almost Herculean task. And the fate of others depended on his success. The ring, the very thing that was entrusted to him, threatened to destroy him.

My daughter's diabetes is my ring. I don't want it. I'm unworthy of doing battle with it. It threatens to overrun my spirit; my very being. And while it will not take my life; it is very capable of taking Elise's life.

To me, Diabetes is the one disease that rules it all (and no, I'm not comparing it to other diseases in this case). What I mean is that it touches every part of your life, and nothing emerges unscathed.

Diabetes rules your relationships. Is there anyone who is reading this who has not lost friendships because of this disease? Has your marriage not been affected? I am also happy to say that I have gained many dear friends due to diabetes.

Diabetes rules your watch. BG check time, shot time, meal time, snack time. Repeat ad infinitum. Almost every hour on the clock seems like it's dictated by this disease, and hardly a minute goes by when you're not thinking about it.

Diabetes rules your calendar. Maybe one day when we're on the pump it won't be like this, but for right now we've had to turn down two birthday parties this month because of the timing. One is in the afternoon, falling right between snack and dinner time. Plus they're serving cake and ice cream. It breaks my heart to think of the fun Elise will be missing. Hopefully one day soon, this won't happen as much.

Diabetes rules your pocketbook. I shudder to think about the amount of money we have poured into this disease. And while I would pay 100 times that amount to keep Elise healthy, I worry that there might come a day when we can't afford it.

Diabetes rules your food. If Elise could chose her favourite meal, it would be pizza and pasta, some french fries on the side and ice cream for dessert. That girl loves her carbs. And while I let her eat all of the above, I try to limit her to one high carb item per meal. But what I hate most is when, at the end of the meal and all her carbs have been accounted for; she asks for one more piece of bread. Or a bit more pasta. And I have to say no. It. Just. Sucks.

Diabetes rules your sleep. Or lack of sleep. Midnight, 3 am, 5 am checks... doesn't leave a lot of room for any shut-eye.

Diabetes even rules your very soul. Do you not feel lonely? Alone? Like nobody understands or even cares? Do you find yourself in a deep funk; unable to get out? Sometimes I feel like if one more thing is added to my life, I am going to go crazy. Some days I am so overwhelmed, all I want to do is sit on the sofa and cry until there are no more tears. I miss the old me. I feel like I'm half the person I used to be.

In the end, Frodo manages to reach Mount Doom and the ring is destroyed. And as much as I wish this could happen with Elise's diabetes, unless there is a cure, it will not. There will come a day where the quest for me is over, and I will pass the ring onto Elise. But there will be no destruction in our tale unless we find a cure.

Until then, I will carry this burden, my ring. It can have everything else in my life, but I will not let it rule me.

Monday, December 27, 2010

Christmas with a touch o' the plague

Christmas has come and gone and though only two days in the past, it's but a hazy memory for me. Mostly because of the aforementioned plague in the title. But enough about the yuck... I've decided to do a post about our Christmas from start to finish. But lucky you, it's mostly with pictures! So, enjoy!

We started off December with the our yearly trek out to the tree farm to find the perfect tree. Well, when it was just Fred and I; it was a search for the perfect tree. When Elise came along, it became the search for a pretty good tree. Then came diabetes, and we were happy with an adequate tree. Now with Mattias is the mix, we're happy to get out of there with a tree.

By the way, managing a three hour drive (round trip), a hay ride, finding and chopping down a tree, and a playground stop on a newborn's and a diabetic's (on NPH no less) schedule and having NO major catastrophes is HUGE! Holla!

loving the tire swing

I love this picture. No shots, no finger pokes, no carb-counting; just a little girl enjoying the day

hay ride!

This tree was Elise's pick

We found it! (why yes, that IS a burp cloth hanging out of my pocket. I am sooo stylin')

posing with the tree

father and daughter

self-taken pic... not sure what is up with my lips. Maybe it's my picture-taking face?

Not gonna let D kill one of my favourite traditions... making gingerbread cookies! These little guys have only 5g of carbs each (including icing and M&M)


Another fun tradition is taking our pic in front of the tree. The post below this one has our finished product.

Self-timer fail... although Elise looks cute!

Christmas Eve we head out to church and then to a nice steak dinner with friends afterwards. During the service, our pastor calls all the children to the front and reads a story to them every year. This year, Elise ran down all by herself. I was kicking myself for not checking her CGM first!

Elise's Christmas dress


You can't tell, but I'm dying in this picture.

Christmas morning, like pretty much every D-family, breakfast comes first. Then it's present time!

This was all the action Mattias saw. He went down for his nap right after this picture.

Note: Seven stalking Elise. Our dog loves to unwrap presents and she was just waiting for her turn!

I think 95% of her gifts were princess-related

Elise LOVED her gifts from our Secret Santa; Thank you Wallace Family from Oshawa, Ontario! If I had known our Secret Santa was Canadian, I would have sent her my list of foods that I miss!

Groovy Girl princess!

Stickers too!

Mattias loved the wrapping paper!

And his car (from Secret Santa)... he happily chewed on that bad boy all day!

If you made it this far, congrats! I know it was a long post, but I though it would be fun to chronicle our Christmas from start to finish!
I got THE coolest present, but that's for another post. This one is too long already!

Wednesday, December 22, 2010

Be Prepared

I was a Girl Guide as a child (Canada's answer to Girl Scouts), and although I didn't really enjoy being a Girl Guide (I was a very shy child and hated to be a part of big groups like that), I took their motto of "Be Prepared" to heart. Mostly because I was born anal-retentive.

I like to be prepared in any situation, for any situation. I do not understand what the words "pack lightly" mean. This lends itself nicely to being the parent of a Type 1 Diabetic; I can't think of any other disease that causes the caregivers to become pack mules.

But I have to admit that I've become a wee bit lazy in my "being prepared". If I'm running out to the store with Elise, I don't always take her insulin with me. I pretty much always have something for a low, but there have been times when we're going to Target or the grocery store and I've forgotten her emergency kit at home. Instead of turning around, I just figure I can grab something at the store if she goes low.

That's why the story in Sarnia
, Ontario has given me great pause. For those of you unfamiliar with the story, motorists were stuck for over 24 hours on a highway due to a snow storm and had to be rescued.

On a side note, when the local news had a blurb about this story, they said it took place in Ontario Canada. Ontario is a pretty big place, folks. Let's narrow it down a bit. It's sort of like saying, "a tornado destroyed a town in Texas. In other news..." I'm just sayin'.

And it made me think... what if something like that happened to us? What if we were stuck somewhere with no access to food or the life-saving insulin my daughter needs? What would we do? Now granted, we don't get much snow here, but it reminds me of something that happened to us last Christmas Eve.

We were coming home from dinner following the Christmas Eve service at our church. It was a pretty bad storm for these parts; snow was coming down sideways. We did okay until we reached an overpass. The problem with overpasses is that they freeze when it's snowing/sleeting and become hills of ice. We tried to go over it, but kept sliding backwards. Other cars were coming behind us and were getting stuck too.

It was growing closer and closer to the time that Elise needed her bedtime insulin (which I did not bring with me) and a snack (I don't think I had any food with me either, she had eaten everything at dinner). Thankfully, Fred is an awesome driver and drove backwards through the maze of cars until he made it to an intersection. We then drove along the feeder road until we could drive under the highway instead of over it. A trip that normally takes 15 minutes took almost 90.

Thankfully, it ended well. But that memory, plus the story out of Sarnia, is the kick in the pants I need to become more committed to being prepared. As the mother of a 3-month old and a type 1 diabetic, I have a lot of crap to haul around with me. But the alternative is just too scary.

So tell me. How do you prepare? What are some of your must have items? Are there any products you just cannot do without?

***Yup, that's a picture of a sassy 5-or-6 year old me as a Brownie (I couldn't find any good Girl Guide ones). Go ahead, laugh. But I think I was cute as a red-headed button.

Tuesday, December 21, 2010

All I want for Christmas

I remember Christmas as a child as an exciting time. Starting when the tree went up, and packages started to arrive in the mail. Slowly, the empty space beneath the tree would start to get filled up by brightly coloured boxes and bags; each concealing their secret that would be revealed on Christmas morning.

On Christmas Eve, I would always sneak down after Santa had come to see the tree in all it's glory. I would marvel at how it towered; the lights casting rainbows in the darkened room. I would take in all the gifts piled at the bottom, then quietly steal back upstairs to my room to await the carnage of the morning.

As you grow older, the meaning of Christmas changes for you. Traditions. Family. If you are religious; Jesus. The gifts slowly fade in importance. But there is one gift I would give anything for.

It cannot be wrapped or bought. It takes away, rather than gives. Of course I'm talking about a cure. It goes without saying that I would forgo gifts for the rest of my life, if I could just have this one thing.

I know I probably won't get it this year. Or the next. Or for many years to come. But it will always be at the very top of my list

Sunday, December 19, 2010

Another post in which I talk about stuff

Let me just start off by saying I've had a perma-grin ever since I woke up Friday morning and saw how much everyone enjoyed the video. When the idea popped into my brain, I thought I'd put it up on my blog, and my fellow D-moms, D-dads and other D-peeps who read my blog might get a few chuckles out of it.

But apparently, it's been shared on facebook (which I'm not on) over 1200 times. And people find it funny, which tickles me to death. Seriously, one of the best things a person can say to me (besides the fact that I'm an awesome wife/mom/substitute-pancreas), is that I make them laugh. So thanks for all the comments, sharing and love!

On Friday we had our endo appointment. I think we have a reason why Elise's numbers have gone coo-coo bananas over the last three or so weeks. In three months she grew over an inch and gained almost three pounds. Holy growth spurt! Things are slowly returning back to "normal-ish".

We did talk about a pump, and I am signed up for an upcoming pump class (not until March - ugh). I'm still debating. How much of it should be the child's choice?

I've talked to Elise about a pump, but I don't think she quite gets it. The only pump she's ever seen is the Omnipod, but I don't think we'll be going that route (unless I see the new version and it is WAY smaller than the current one). She didn't seem all that excited about it anyway, except to say she wants a pink one.

I almost forgot... A1C came back at 7, which is exactly the same as three months ago.

To quote the Talking Heads, "same as it ever was." And I'm okay with that.

Thursday, December 16, 2010

What not to say... the video

I couldn't resist. When I saw a similar video about things people say to the parents of multiples, I thought, "Somebody totally needs to do one for diabetes."

Then I thought, "I should totally do one for diabetes." So I did. First, I re-read the very funny post by Kelly Kunik, and the hilarious comments and incorporated some of them into the video.

I wish I had more time to make it better, but this finished product took me almost 8 hours to make; not 8 straight hours mind you, but 8 hours of me doing 5 minutes here and 5 minutes there.

So enjoy. Sorry Reyna, that I didn't incorporate any bad - er - colourful language into it. Little ears were listening. I was even admonished for using the word "stupidity".

For those of you who cannot see it on my blog, click here for the YouTube link.


I'm not sure "blurgh" is really a word, but it's how I'm feeling. Tomorrow we have our endo appointment, and usually I have a pretty good idea on where we stand. But for once, I have no idea.

Hopefully we'll get some answers on why Elise's BG is soaring and plummeting at dinnertime. She can go from 130 flat to 300 double arrows up and 150 double arrows down all in the span of an hour. That cannot feel good. We have tried all sorts of tricks (short of giving her two shots), and nothing seems to be working.

The other night when she had her skating lessons, I withheld her shot for about an hour after she started eating. She was in the 300s when I put her on the ice, and when she came off 30 minutes later, she had double arrows down on the CGM and her BG was 82. Blurgh.

(I'm even thinking of giving her a low-ish carb meal - about 20g - for dinner, and not giving her a shot at all, just correcting at bedtime on skating nights. Anybody have any thoughts???)

We'll also be discussing pumps at our appointment, and I'll be trying to weasel out of pump classes (at least one of them that our endo makes you take). A pump seems to be in our imminent future, but I'm not looking forward to trying to figure out which one to go with and then starting the learning process over again. The mere thought of it exhausts me. Blurgh.

Today Elise told me her heart hurts. What the crap does that even mean??? Blurgh.

And today is Elise's pre-school teacher's last day. Miss C has Type 2 Diabetes (dx about 1 1/2 years ago), and she's having trouble managing her BG. So she's leaving her job to get a better handle on it. If you ask Elise what her favourite thing about school is, her answer is, "Miss C!"

I can't say enough about how this woman has helped Fred and I to feel completely comfortable with leaving Elise with anyone for the very first time in her life. Because of her, we were able to take this step, and Elise is so much better for it. Miss C went above and beyond for us, and I am so sad that she has to leave. I understand, but I'm still sad. Today Elise told me, "I'm going to miss Miss C!"

My in-laws are coming tomorrow and my house is one big trash heap. Instead of complaining via a blog post, I really should be cleaning. So I'm off to find my vacuum.

Say it with me... BLURGH!

Tuesday, December 14, 2010

Do you hear what I hear?

Some time ago I saw THE best Christmas cards in a store. On the front of the card, there was a choir of people wearing those oh-so-wonderful backless hospital gowns. They were singing, "Do you hear what I hear?". The caption on the card said, "Christmas at the mental hospital".

Funny? You betcha. Politically correct? Probably not. What does it have to do with this post? Not a whole lot, except these days Fred and I find ourselves saying, "did you hear that?" to each other a lot.

If you or your child has a CGM, then you are well-acquainted with it's many alarms; of the buzzing and beeping variety. My ears are finely tuned to be able to hear these alarms at all times.

The problem is that there are probably no fewer than 8 different items in our house that make similar sounding (or similar enough sounding to my very tired and very overworked ear drums) noises. Fred's Ipad, my laptop, my phone, Fred's phone, the smoke alarm, microwave, stove alarm, furnace (yes our furnace makes a buzzing noise. I'm told that it's okay) ... and that's not even counting the plethora of Elise's toys that boop, beep or buzz in some manner.

It's enough to drive a person crazy. Although for me, it's a very short trip.

Just today, I was sitting on the sofa with the TV on. Elise was in her room, having her "rest time" (since she recently decided not to nap anymore, I still send her upstairs for an obligatory momma-needs-a-break-from-YOU time), when I heard a very distinct buzzing.

Now usually Elise will call to me through the baby monitor, saying "my phone is ringing!" (and ohmygoodness that STILL tickles me that she says that) But there are days that she does fall asleep, so I lugged my behind upstairs to find her wide awake and a 105 flat on the monitor. Weird.

I decided it must have been on of the other noise-makers in the house and went back to my business of killing brain cells. It wasn't until a few hours later when I happened to be passing by the TV (which was still on) and heard the buzzing again. Turns out it was some stupid commercial!

It's so interesting to me that something that is just an every day noise to other people, causes us D-parents to snap to attention. My favourite is when Jessica, Laura and I are all hanging out and we have to figure out which of our kids is doing the buzzing or beeping.

Maybe Dexcom could have a music player on their next receiver... that way, instead of a buzz or a beep when Elise is low, it could play "Low" by Flo Rida.

I'm just sayin'... we've got to get our chuckles where we can.

Monday, December 13, 2010

They did it!

I am always in awe when a person with diabetes takes on very physically demanding challenges and does well. If you haven't read Reyna's posts about how she keeps up with her energizer-bunny-of-a-kid Joe, you should. Just reading them makes me want to take a nap.

Because let's face it. Diabetes and activity of any kind is not easy to manage. And the Amazing Race is physical activity on crack. And that's what makes this season's win by Nat (PWD) and Kat that much more incredible.

Nat and Kat were, without a doubt, my favourite team in race history. Diabetes aside, I have never seen a classier team run the race. I don't think I heard them utter a cross word to each other once, and I also read that Kat helped Nat out with a lot of the diabetes management.

I am not ashamed to admit that I cried when I saw Nat and Kat running for the finish line. Elise was watching with me, and I just lost it. I became a blubbering mess of mommy goo.

Because it means so much to me to see someone with diabetes prevail. Through the extreme heat. Extreme cold. Exhaustion. Hunger. Hardship. Fear. Different time zones, cultures and food. Nat not only made it through, she and Kat came out on top. And the first all female team to win it too!

I'm sure Nat Strand didn't set off on this adventure to become a role model, but I think she has. To all the kiddos out there who think diabetes might hold them back. To all the parents who fearfully wonder how this disease could limit their child.

Congrats and thank you Nat and Kat, for running such a classy race. I loved seeing two smart, sassy, and determined ladies take the top prize!

Friday, December 10, 2010

BG Nirvana

Things have been going so terribly BG-wise the last few weeks, I thought I would take the time to celebrate today.

That huge spike and drop you see is dinner last night. She goes crazy high and them plummets back down. I'm slowly trying to figure it out

Oh sure, I was up three separate times last night to deal with a low blood sugar, but we started off the day at 151, and that's the highest she's been so far. Her BG today has ranged from 80 - 151. Aside from that spike, that's a pretty good-looking 24-hour graph.

Even better, that first mountain (more like a hill) you see in this pic below is Elise coming down while she's eating her breakfast. Note, there is no post-meal spike. Ha, I totally made breakfast my bitch today. Dinner... you're next.


Wishing you a Merry Christmas!

Wednesday, December 8, 2010

If I don't get off this coaster soon, I just might vomit

As I was perusing my D-Mom and D-Dad blogs a few days ago, I noticed a common thread... there are a lot of us riding the glucose roller coaster right now. And I'm wondering what planets are in alignment to unleash this hell upon us.

For us, it started off with just dinner problems; we had to start giving Elise her insulin about 25 minutes after she started eating because if we gave it any sooner, she would drop low, we would have to give her some fast-acting carbs, then she would sky-rocket from all the extra carbs.

But it's still not a fix... as we watch the CGM we see that she holds steady while she's eating (once we had a record 45 minutes steady BG, she didn't start rising until after she had finished eating). We usually give her the shot as soon as we see the slanted arrow up appear. Unfortunately with this method, we get double arrows up into the 300s, then double arrows down. All in the span of an hour. If I give it any earlier, she crashes.

Tonight, she was 151 going into dinner. I gave her 1.5 units for almost 40g of carbs. She held steady for 25 minutes and started to go up. I gave her the shot, and in 30 minutes, she's almost at 300 with double arrows up. I looked at the CGM 20 minutes later and she's at 179 with double arrows down. And 15 minutes after that, she's 96, double arrows down. She's 84 via her meter, so I give 7g. Now I'm just waiting for the spike to happen (and it will).

My brain is so fried from trying to figure this out. This issue only happens at dinner. Her ratio at dinner is now over twice what it is in the morning. I think our next step is to go back to diluted insulin at dinner time. I can't stand to see the peaks and valleys on the CGM, but I'm too afraid to take it off of her for fear of missing a crash.

I have never felt this helpless, useless, and downright hopeless before. Nothing we try has worked. And it's got me in a funk. I think we've had smooth sailing for so long, I don't have the capacity to deal when I can't figure it out. If you've been reading my blog for awhile, you know that we don't bother with the CDEs at our endo because they have proven themselves useless time and time again. Talking to them would drive me to tears.

Thankfully, we do have an endo appointment in 9 days. But I don't think I'm going to last that long.

Tuesday, December 7, 2010

She's a natural

CGM before lesson: 94, double arrows down
Actual BG: 74
Extra carbs consumed: 14g
Watching your child partake in something that is near and dear to your own heart: PRICELESS!

So you can suck it diabetes, nothing's going to stop this girl from enjoying her Canadian roots!

Sunday, December 5, 2010

Always something there to remind me

Do you know what I hate? That diabetes never completely leaves us alone. It's always there, like a nosy neighbour who comes knocking at the most inopportune times, intent on driving you crazy.

Mattias has reflux. Bad. Like, 60-plus-burp-clothes-are-not-enough bad. Like, 8-outfit-changes-in-a-day bad. If reflux was an Olympic sport, he would win the gold medal, earning perfect 10s for volume, accuracy, and number of times. You get the idea.

In the last few weeks, I noticed his feedings started to taper of. I wondered if 2-month old should only eat six times a day. Then, the length of nursing started to shorten too. He would wake up in the morning and feed for only 6 minutes on one side, and be done. If I even attempted to make him feed more, he'd scream.

Otherwise, he seemed fine. Growing, smiling and just generally being the good baby that he is.

My major freak-out happened last Saturday. He hadn't eaten in 5 hours because we were out running errands. He seemed happy enough until we got home and I tried to feed him. It was like I was torturing him. He refused to eat. He had done this a few times before, but I could always get him to feed if I just waited it out. This time he wasn't having it. And this brought out crazy Joanne.

Because this situation is so terrifyingly familiar. At about 8 months, Elise went on a nursing strike. Same sort of deal (minus the reflux). I thought maybe she was wanting to wean, but I wasn't ready for that, so we fought through it. It took about a month, and she came around. And started feeding more and longer than ever. Now I know why.

Because a few months later, she was diagnosed with diabetes. And now my mind is going there with Mattias. I can't help it. That Saturday I even checked his BG. It was 115. But I start to think... he hasn't eaten in 5 hours, shouldn't it be lower? True, he was VERY agitated. But... what if?

The hard part is that there are so many variables. The reflux... but he seems to be okay and doesn't cry when feeding anymore.

My thyroid level was high and my meds had to be adjusted. Over-active thyroid interferes with milk production. But if he's not getting enough, wouldn't he want to eat MORE?

I do have a history of making too much milk. Maybe he's getting enough in those first few minutes. But when I pump, I usually only get an ounce or so out of the side he didn't feed on. And sometimes his diaper is still dry after 3 hours.

So many questions, and I don't have any answers. He's been to the doc, and she says he looks good. No sign of infections. Gaining weight (for now - she says it could take a few weeks for his weight to slow down if he's not getting enough). He seems content. Rarely cries and loves to smile.

And yesterday he started feeding well again. And I was happy. Until I remembered what happened with Elise. And there was diabetes again, knocking on the door and wanting to be let in.

Mattias being diagnosed is not what scares me the most. I'm afraid I'll miss the signs; convince myself that it couldn't be, and he could get very sick. Right now I think about it to the point of being obsessed, and I have to hold myself back from checking his BG.

I just need a break. From the fear. The obsessing. But mostly, from Diabetes. Somehow I don't think that's going to happen.

Friday, December 3, 2010

I'd like to accept this award...

Okay, so I'm a bit of a slacker... I've been wanting to do this post but have had other things to blog about first. Better late than never, I suppose. Here are the rules of the award:

1. Thank the person who gave me this award
Tracy (Superhero and the Princess), Denise (My Sweetest Boy), and there might have been one more, but it escapes my tired brain at the moment... please feel free to speak up if it was you!)

2. Share 7 things about myself

-I will not shop at Walmart. I don't even care about the money you can save by shopping there. I have had too many instances of bad customer service and when I contacted them about it, their attitude was basically, "we don't really care". I refuse to spend my money at a business that doesn't value me as a customer. Now Target, on the other hand, rocks!

-I'm really quite shy when you first meet me. Some people have told me I come off as snobby. But once you get to know me, I NEVER shut up!

-I find fart humour and poop jokes funny. I'm really just a 12 year boy at heart.

-I can speed read. Not as fast as I used to, but I can read a 400 page book in a few hours. I LOVE to read, but don't have that much time to do it anymore.

- I am an avid people watcher. Fred makes fun of me because I have no self-awareness and don't even try to hide the fact that I'm staring. Elise seems to have inherited this trait.

-I am a money-saver extraordinaire. At the height of our debt, Fred and I owed over $75,000 in credit card debt. We became debt-free (except for our house) on our anniversary in 2005(it took us four years). I once paid around $2 for over $100 worth of groceries. Yes, I love coupons!

-One of my dream vacations is to do a bike trip through Ireland. The other is to see every major waterfall in the world. Hopefully we'll win the lottery soon, which would be a Festivus miracle if it happened, since we don't play.

3. Pass the award on to 12 bloggers you have recently discovered and who you think are fantastic

I'm going to cheat here and say, if you haven't done it yet, consider yourself nominated!

Thursday, December 2, 2010

Things I learned about diabetes this month... November edition

-Thanksgiving is the best when done with another D family. Fred and I are not from the U.S., so Thanksgiving is not a big deal to us. We usually get invited to someone's house. Since Elise's dx, Thanksgiving has been hard. Because she need to eat at a certain time (and not 3 pm which seems to be the norm for some strange reason). Because we need accurate carb counts. Because I will probably drive you crazy with all my weighing and calculating. This year, we ate with Jessica and her family. That girl can COOK! And she even figured out all the carb factors for the foods and made the most adorable list of them, complete with drawings. She sent it home with me... I must remember to scan it! The best part was how they get it. And it was awesome.

-When you check your baby's BG on the heel, you should not poke them in the middle if the heel, as the lancet could hit the bone and cause an infection. Rather, you should poke them on the side. This is per Mattias's pediatrician.

-Diabetes is going to cost me my teeth if I don't do something. All the stress from D-management gets taken out on my choppers at night. I grind my teeth big time. The other day, part of my tooth came away as I was flossing. I went to the dentist and he said it probably broke because of all the pressure I put on my teeth from the grinding. Greatness. Now I need a night guard. Merry Christmas to me.

-My daughter is a sugar-holic. She actually is disappointed when she's not low because she doesn't get any smarties. We had just started using those plastic wrapped bundles-of-pure-sugar for lows because we received a bunch of them at Halloween. I had to stop because of Elise's smarties jones. It would only take about 5 or 6 of those little suckers to get her back in range, but she'd cry when she didn't get the whole package. So now we're back to using bananas for lows. Plus I like to sing, "these lows are bananas, B-A-N-A-N-A-S". Because I'm weird like that.