Anyway, here's some pics of our little Halloweenies!
Sunday, October 31, 2010
Halloweenies
Anyway, here's some pics of our little Halloweenies!
Thursday, October 28, 2010
Naked Pancreas!
1. What kind on insulin management mode do you use?
MDI, for right now. We also use a CGM. Her name is Eileen.
2. How often do you inject/change pump sites?
Elise gets 3 shots a day, breakfast (a combo shot of two insulins, sometimes three if she's high when she wakes up), dinner, and bedtime.
3. What type (s) of insulin do you use?
We use NPH at breakfast and bedtime, humalog at breakfast and dinner, and diluted humalog to correct highs.
4. What are your basal settings ?
3 units of NPH in the morning, and 2 and a bit units of NPH at night. Yes... that bit is soooo scientific. But if we do 2 units she goes high, and 2 1/2 units makes her go low. So 2 and a bit it is!
5. What are your correction factors ?
1:100
2:200
Remember, she's on diluted insulin for corrections.
6. What are your meal ratios ?
Breakfast - 1:15
Lunch - no shot, she gets between 20-25g of carbs
Dinner - 1:18
Elise also gets 3 uncovered snacks:
10:30 am - 15g
1:45 pm - 5-15g, depending on BG
8:30 pm - 15-20g, depending on BG and level of activity before bedtime
7. What do you do for activity and/or PE?
I monitor like crazy and carry a pocketful o' carbs (that is totally going to be my band's name when I form one). The CGM has been awesome in these circumstances. Activity makes Elise drop like crazy, so I usually just give her more carbs during her snack times to keep her level.
8. How do you manage Pizza, Macaroni and Cheese, or any other "difficult to manage" foods?
We find if we limit the amount of "difficult" foods, it doesn't make her BG go crazy. One piece of pizza doesn't seem to affect her and neither does a scoop of ice cream.
9. How do you prefer to manage your logs/data?
We write everything in a log that Fred designed for us. Seeing all those numbers right in front of me really helps when I need to make changes.
10. What's your A1c?
Dx (Sept '08) - 6.5
Jan. 2009 - 7.7
May 2009 - 8.9
Aug. 2009 - 7.9
Nov. 2009 - 7.0
Mar. 2010 - 7.1
June 2010 - 6.6
Oct. 2010 - 7
Woo! Naked meme... who wants to streak with me?
Tuesday, October 26, 2010
School report card
Fisrt off, Elise's teacher (who is type 2), printed up a slip of paper that she writes Elise's pre-snack BG, how many carbs she ate, as well as her pre-playground and post-playground numbers on. She then gives it to us at the end of class so we know exactly what went on with Elise's BG while she was away from us. Her teacher did this completely on her own and with NO promting from us!
Then, as I was dropping off Elise today, the teacher pointed out the Mom who is bringing snacks for the Fall Party on Thursday (more on that in a second). I needed to know a bit more info on what she was bringing.
The mom described what the snacks were, and then APOLOGETICALLY said, "I know, they're pretty carb-heavy... I'm sorry."
Holy crap-on-a-stick, did she really just say that? Turns out she had gestational diabetes and her FIL has diabetes as well (not sure which type). She then said she would be happy to bring something with fewer carbs. Wow.
Here is my delimma about the Fall Party. The school usually gives the kids their snack at 10:00. The party is at 11:00, during which they will get another snack (what the mom is bringing). As you may know, Elise is on NPH, which lets her have a 15g uncovered snack at around 10:30 (on school days we just let her eat a bit early), then she has to eat lunch pretty much at noon (right after school is over), when the NPH is in full effect (the downside is the strict schedule, the upside is one less shot).
Sooo, what do I do? My thought is to let her have a carb-free snack at 10:00 (so she doesn't feel left out at snack time), then go up to the school and try to figure out the carbs in the party snacks. The hard part is, 11:00 is really too close to lunch and it will make the rest of her numbers so screwy. Plus the snacks (Halloween chex mix, pigs in a blanket, and rice krispies) are bound to send her BG through the roof. I think like most of what I do, I'll just have to wing it and give my best WAG.
This new chapter in our lives has us looking at our pump options. We always said we didn't mind the strict schedule of NPH as long as it worked for us. Well, it's starting to not work. Unfortunately, when we inquired about pump classes we were told there isn't any availabiblty until March. Looks like I'm going to have to get a bit pushy.
I guess our next step is to pick which pump is right for us. That should be easy... NOT!
Sunday, October 24, 2010
Walk to Cure Diabetes 2010
North Texas:
Wagon ride with Grandma Cheryl
Thursday, October 21, 2010
At a loss of words, for once
Though I feel like I should say something.
Maybe it's because since I heard the news that we had lost another member (and a child at that) of the diabetes community to Dead in Bed Syndrome I have tried my absolute hardest not to think about it.
But it's there anyway.
It's there in the way that tears start to fall any time I allow my mind to go there.
It's there in the way I find myself so freaking mad that diabetes is my daughter's reality.
It's there every single time I haul my tired ass out of bed to make sure Elise's is still breathing.
It's there when I pray for a cure.
It's there when I hug her for about the hundredth time today.
It's there when I don't want to let her go. Ever.
I am so totally heart broken for the family that lost their 13 year daughter to this insidious disease. I cannot imagine the pain. In fact, I'm expending a whole lot of energy trying not to.
Instead, I will add my voice to the rallying cry for a cure.
Let it come soon.
Tuesday, October 19, 2010
We did it!
She did amazing and never even looked back when we left her. I, on the other hand bawled like a baby.
Diabetes-wise, everything was okay... she has been high since yesterday, and remained high throughout the morning. Even this afternoon we're having trouble bringing her down. But high is better than the alternative.
Right before I woke up, I had a dream that her BG was 742 and her ketones were 9. Can you tell I was a bit stressed about the whole situation?
The best part? She absolutely LOVED it. She told me her favourite part was cleaning up, and she made lots of new friends one of which she danced with. And I got to spend some unhurried snuggle time with Mattias. I think I could get used to this sending-her-to-school thing!
Check out these cute pics of Elise:
Monday, October 18, 2010
Two Quick Questions
First, those of you on MDI (or remember when you were) do you find you find the insulin is less/more effective depending on which site you use? The reason I ask is because we just started using Elise's tummy, and it seems when we use this site, the insulin is more potent and we experience lows.
Number two: We just got an email that a student at Elise's pre-school was diagnosed with hand, Foot and Mouth disease. He goes on a different day, but is in the same room. We called Elise's teacher and she assured us that they wipe everything down at night, and make the kids wash their hands before and after snack time as well as after they use they playground (and the bathroom, of course), but I'm wondering if we should send her tomorrow.
If you read my last post, we had pretty much decided we were going to send her despite her crazy numbers, but this latest issue may have changed my mind.
What do you guys think? Am I just being way to over-protective? The last thing we need is an illness around here.
Take this D and shove it
But most of it is because we have not figured that freaking full-strength insulin crap out. And I'm a little frustrated, can you tell?
I can give her the same dose at breakfast, same food, same EVERYTHING and she either goes crazy low, or crazy high. There is no in between with this stuff. Plus her blood sugar is roller-coastering all over the place. Today, only 45 minutes after breakfast, she went down to 63 and skyrocketed to almost 400 after lunch. I didn't go crazy on the carbs for the low, because
she was 132 right before her lunch.But on other days, she stays in the 200s right after breakfast up until about 3:00 pm, when she starts to go down.
I don't get it, and I am so afraid to send her off to school if she's having these lows (which she does every other day or so). I don't even know where to start to make changes and I freaking HATE the fact that we can't even turn to the CDEs for help.
I think the worst part is how it's affecting her behavior. If she's sporting any kind of attitude or throwing a tantrum, it's always when she's rising or falling fast on the Dexcom. It's getting downright nasty these days and we're kind of at the end of our rope on how to deal with her.
Part of me wants to go back to using diluted, because we never saw her numbers roller-coaster like this before. But I know we just need to try and figure it out. Right now is just a bad time to be doing it.
To top everything off, Mattias has reflux something terrible. He spits up at least 5 times after every feeding (that's per side, not the whole feeding). He is so miserable all the time, even though he's on medication. I think yesterday I changed his outfit 8 times and it seems that all I do these days is laundry.
I don't think I'd be as stressed about this if it wasn't for the fact she was starting school tomorrow. How do you guys handle making adjustments on days when your kids are away from you? Should I keep her home until we somewhat get a handle on this?
Man oh man... it's a "diabetes-can-suck-it" kind of day.
Friday, October 15, 2010
Elise is IT!
What is your name?
Elise C (gives full last name)
How old are you?
(holds up three fingers) 3!
When were you diagnosed with diabetes?
I don't know
Do you remember what happened when you were diagnosed or how you felt?
Not good
Do finger pokes or shots [or site insertions/infusion set changes] hurt?
Yes
What is a high number?
31 (Well, she IS only 3... and half Canadian. Maybe she's measuring in mmol)
What is a low number?
3... E-L-I (at this point she starts to spell her name). Technically, she's right, again if she's measuring in mmol
What does low blood sugar feel like?
Feels like you need to eat something
What’s your favorite way to treat a low?
Bunnies (Aunt Annie's fruit snacks), bananas and goldfish crackers!
How do you feel when your blood sugar level is high?
Not good
What’s the best thing about having diabetes?
Lots of food (?)
What’s the worst thing about having diabetes?
My sensor (inserting the Dexcom sensor)
Do you worry much about diabetes?
Yup (she wouldn't elaborate)
If one of your friends were diagnosed with diabetes, what would you say to that friend?
You need to have a shot and foods
What’s your favorite food?
Yogurt and apples
What’s your favorite snack?
Granola
What’s your favorite low-carb food?
Salad
Do you know what a blog is?
I don't know
Do you know that I blog about diabetes?
Yes
Do you care?
I don't know
Why do you think I blog about diabetes?
Because I have Diabetes
What’s your biggest wish?
Chocolate
Who’s your best friend?
C (a friend of hers that moved away)
What do you like about him/her/them?
Sharing and playing
What’s your favorite thing to do?
Playing with trains
Do you have a hero?
What's a hero?
What do you want to be when you grow up?
A tiger
Who’s your favorite person in the whole wide world?
Momma
Are you afraid of anything?
Monsters and gorillas
Fill in the blank. (Your name) is___________. There is no right or wrong answer.
Elise
Well, that was fun! When we were done, Elise asked if I had anymore questions for her. I think she enjoyed being interviewed. I think it would be fun to revisit this meme every year, just to see how her answers change.
Wednesday, October 13, 2010
A new chapter
Every time I read that, it struck my little 10-year old brain as very sad. I don't know why, it just seemed so empty to me, so without hope. I guess maybe I focused on the last part too much.
Now that I've given you a glimpse into the beginnings of my little glass-half-empty mentality, I'll get to my point.
Remember that pre-school I blogged about a few weeks ago? Fred and I went to visit them last week, and were very impressed with what we saw. The director took us for a tour, and asked a ton of questions about Elise's diabetes, and what their role would be if she because a student there. About a week later we received a call saying they would love to have Elise come to their pre-school!
Today we met with the lady who will be her teacher. We were told that she had type 1, but it turns out she's actually type 2. To me, it's no big deal... she knows how to check a BG, she understands about carbs, and she seems so on top of things. She even took it upon herself to do some research before the meeting.
We went over Elise's needs, showed her the CGM and all of Elise's supplies. We even had a low BG while we were there, so it was good for her to see how we treat it. I was impressed at how proactive she was, especially when she asked if she could check Elise's BG during the meeting (at a time we would normally be checking, of course).
The school was ready for Elise to start this Thursday (tomorrow), but we're still tweaking her insulin since the move to full-strength and I don't feel like we have it right yet. So Tuesday will be Elise's first day of school!
And now that inscription has taken on a whole new meaning. Yes, I am afraid of letting her go, but I love Elise. And she needs me to let go of her so she can start to find her own way in this world. Yes, even at the tender age of 3, she needs to start taking those baby steps towards independence. And because she is mine, I can always feel confident that she will come back.Especially since she will be so loved and well cared for while she's away.

