Today we had plans to see a movie with the Roses, you know, Wendy from Candy Hearts.
I had a work event and had Wendy come join us to help me with the kids. I ended up not having to "work" the event, but we still got to go and enjoy Kung Fu Panda II.
For some reason, when Wendy and I get the kids together SOMETHING always happens. And it usually involves my kids.
Remember the Playdate at the Mall from last year?
There was also the time when I went with Wendy and Heidi to the Children's Museum and we lost The Superhero and The Princess a couple of times EACH. One of those times The Princess was down the hall in a completely different room, doing art, like a big girl, and all by herself. Both Wendy, Heidi, and their kids were life savers at the museum helping me find my wandering children.
Then there was the time we were at a Diabetes potluck with several friends (Wendy and Heidi included, along with several others) and I lost The Superhero. There was a Relay for Life going on at the same time and he thought some other kids were headed over to the splash area, which was near the Relay and LOTS of people. Wendy found him down the sidewalk. He came back and I tested him, he was low. As much as I don't want to lose a kid, I really don't want to lose a Diabetic kid who is low. Not a good situation. Thank God Wendy helped find him and bring him back.
Well, today was no different.Never a dull moment when out and about with The Ripley kids.
We all went and enjoyed our movie. Only a few minor issues as my kids fought over which of Wendy's girls they were going to sit next to. They seriously LOVE her kids.
On the way out of the movie The Superhero and The Princess were "playing" with the Dippin' Dots machine. I grabbed one of The Princess' hands and got her to leave the machine. She started crying, I thought her hand just got stuck and "hurt" in the machine. I kissed her hand and thought all would be better. Then Sugar (Wendy's D kiddo) said she thought she saw red on The Princess' fingers. I put her down and took a closer look. Sure enough, she sliced 2 of her fingers. I have NEVER needed bandaids before when out and about, so I didn't have any. Thank God for Wendy again, for having bandaids in her purse. We bandaged up The Princess' fingers and moved on.
We went to McDonald's for lunch with all the kids. The kids went to play while Wendy and I ordered. The Superhero was 77 prior to playing and I gave him a juice before letting him run off. When I came back with the food a few minutes later, I called the kids over. The Princess came right down and started eating. I heard The Superhero saying he was scared. I looked and he was up HIGH in the play structure. I don't know why he does this to himself because he HATES heights and he hates seeing through the "floor". He was NOT coming down. And I feared a low, since he was 77 and I was not sure he was coming up yet.
We ended up sending Sugar in with his meter to check his blood sugar. We wait, she was checking, when we called up to see what his number was....ERROR 5! You have got to be kidding me! Of all the times to get a darn Error 5! Seriously?!
Before I knew it, Wendy was climbing up the play structure to get The Superhero to come down. And once he was down, and Sugar was down, I found out she did a second check and he was 98. Thank God he wasn't low. Thank God for Sugar testing him. And Thank God for Wendy climbing in and "saving" him! Thank you God, for The Roses.
After that, there was NO more climbing high up. Just lots of running around and enjoying time with friends.
And to end our day, we went to The Superhero's Endo appointment. He has gained 2 pounds, grown 1 inch, and his A1C went from 7.3 to 7.6 this time around. With the crazy highs lately and his current sinus infection, I'll take it!
*Disclaimer: I am a mom of a T1 Diabetic child and a child with ITP/Asthma/Dysphagia. I am NOT a doctor. I just play one in real life. Please do not take anything in this post or any other post on this blog as medical advice. If you have questions or concerns of your own, please seek advice from your doctor.*
Tuesday, June 14, 2011
Blogsitting today! Check it out...
This week Hallie is leaving for vacation and has several awesome D Mamas blogsitting for her while she is away.
Today is MY turn, and it is an awesome recipe I am sure you will all love.
So click on over and check it out!
CLICK HERE!
ENJOY!
*Disclaimer: I am a mom of a T1 Diabetic child and a child with ITP/Asthma/Dysphagia. I am NOT a doctor. I just play one in real life. Please do not take anything in this post or any other post on this blog as medical advice. If you have questions or concerns of your own, please seek advice from your doctor.*
Today is MY turn, and it is an awesome recipe I am sure you will all love.
So click on over and check it out!
CLICK HERE!
ENJOY!
*Disclaimer: I am a mom of a T1 Diabetic child and a child with ITP/Asthma/Dysphagia. I am NOT a doctor. I just play one in real life. Please do not take anything in this post or any other post on this blog as medical advice. If you have questions or concerns of your own, please seek advice from your doctor.*
Thursday, June 9, 2011
Virtual 5K
Yep, that's right! A VIRTUAL 5K! If you haven't read about it yet, here are the details.
One of my favorite D Mama bloggers, Reyna over at Beta Buddies, has a super awesome sister. Her sister has come up with the idea to do a virtual 5K. This way, we can raise money for JDRF AND get active at the same time!
For all the details check out Tara's blog HERE. The cost is only $10 per person and ALL the money goes to JDRF.
There are prizes up for grabs and most importantly, we are raising money for a GOOD cause! I challenge ALL of my friends to sign up and walk/jog/run the 5K during the weekend of June 24-26th.
Go ahead, go sign up, now...HERE. And enjoy being active for a good cause!
*Disclaimer: I am a mom of a T1 Diabetic child and a child with ITP/Asthma/Dysphagia. I am NOT a doctor. I just play one in real life. Please do not take anything in this post or any other post on this blog as medical advice. If you have questions or concerns of your own, please seek advice from your doctor.*
Wednesday, June 8, 2011
Last night...
Last night.
Last night was one of the worst nights we have ever had.
Seriously sucked.
I will use our Dexcom graph to explain what took place...
Not sure where the 300's came from at dinner time. We bolused. He ate (cereal!). We bolused. He went HIGH. We changed his pump site. We bolused.
He seemed to come down fine. A little too much. We gave him a small "snack" before going to bed. When I went to bed at 10:30 Dex said 197 with a slanted arrow up. Rod was already sleeping in The Superhero's bed (he fell asleep with The Superhero). I went to bed.
1:30am. I wake up to The Superhero SCREAMING. I thought he fell out of bed and ran to his room. Rod was still in there and The Superhero was just SUPER upset. He said he heard a noise that scared him. He was genuinely SCARED. It was horrible to see him THAT scared.
I immediately grabbed Dex to see what we were dealing with.
I saw this...
Dex had said something in the 80's, but it looked like he had been LOW for 4 checks before going back up to the 80's. I did a finger check, 65!
I have no idea if he really went LOW (below 40) or not. We were sleeping. It was about 15 minutes after the LOWS that we were woken up to the screaming. I am really hoping he was laying on it weird and he didn't go THAT low.
But, if he did, THANK YOU GOD for keeping my boy safe while we were sleeping! And THANK YOU GOD for him waking when he did!
We treated the low with snacks. I also started a temp basal decrease. I had a feeling the lower numbers came due to the site change (often happens with new sites). And of course lots of hugs were given out. He was SO SCARED.
Rod and The Superhero got up and went to the couch. The Superhero was still SCARED. They were going to watch some TV for a bit.
Apparently when my temp basal decrease ended, The Superhero started to drop again. Rod treated and started another minus temp basal to get through the rest of the night.
This time, definitely over treated a bit. It is all such a "guessing" game.
I woke up at 5:30am to find The Superhero STILL awake on the couch. I told both Rod and The Superhero that he needed to go back to sleep, even if only for an hour. He has art class today and I am NOT taking an overly tired, cranky child with me.
I was happy to see when I woke up at 7, that both boys were sleeping on the couch.
I was not happy to see The Superhero had been HIGH for a couple of hours (to no fault of anyone, but Diabetes). Ugh.
An hour and a half later right now, and he is down to 367. I am RAGE bolusing this morning and need to get him DOWN.
Especially since he wants cereal for breakfast. I told him his blood sugar has to have a ONE in front of it.
I hate Diabetes. No silver lining. No rainbows. No unicorns here today.
*Disclaimer: I am a mom of a T1 Diabetic child and a child with ITP/Asthma/Dysphagia. I am NOT a doctor. I just play one in real life. Please do not take anything in this post or any other post on this blog as medical advice. If you have questions or concerns of your own, please seek advice from your doctor.*
Last night was one of the worst nights we have ever had.
Seriously sucked.
I will use our Dexcom graph to explain what took place...
Not sure where the 300's came from at dinner time. We bolused. He ate (cereal!). We bolused. He went HIGH. We changed his pump site. We bolused.
He seemed to come down fine. A little too much. We gave him a small "snack" before going to bed. When I went to bed at 10:30 Dex said 197 with a slanted arrow up. Rod was already sleeping in The Superhero's bed (he fell asleep with The Superhero). I went to bed.
1:30am. I wake up to The Superhero SCREAMING. I thought he fell out of bed and ran to his room. Rod was still in there and The Superhero was just SUPER upset. He said he heard a noise that scared him. He was genuinely SCARED. It was horrible to see him THAT scared.
I immediately grabbed Dex to see what we were dealing with.
I saw this...
Dex had said something in the 80's, but it looked like he had been LOW for 4 checks before going back up to the 80's. I did a finger check, 65!
I have no idea if he really went LOW (below 40) or not. We were sleeping. It was about 15 minutes after the LOWS that we were woken up to the screaming. I am really hoping he was laying on it weird and he didn't go THAT low.
But, if he did, THANK YOU GOD for keeping my boy safe while we were sleeping! And THANK YOU GOD for him waking when he did!
We treated the low with snacks. I also started a temp basal decrease. I had a feeling the lower numbers came due to the site change (often happens with new sites). And of course lots of hugs were given out. He was SO SCARED.
Rod and The Superhero got up and went to the couch. The Superhero was still SCARED. They were going to watch some TV for a bit.
Apparently when my temp basal decrease ended, The Superhero started to drop again. Rod treated and started another minus temp basal to get through the rest of the night.
This time, definitely over treated a bit. It is all such a "guessing" game.
I woke up at 5:30am to find The Superhero STILL awake on the couch. I told both Rod and The Superhero that he needed to go back to sleep, even if only for an hour. He has art class today and I am NOT taking an overly tired, cranky child with me.
I was happy to see when I woke up at 7, that both boys were sleeping on the couch.
I was not happy to see The Superhero had been HIGH for a couple of hours (to no fault of anyone, but Diabetes). Ugh.
An hour and a half later right now, and he is down to 367. I am RAGE bolusing this morning and need to get him DOWN.
Especially since he wants cereal for breakfast. I told him his blood sugar has to have a ONE in front of it.
I hate Diabetes. No silver lining. No rainbows. No unicorns here today.
*Disclaimer: I am a mom of a T1 Diabetic child and a child with ITP/Asthma/Dysphagia. I am NOT a doctor. I just play one in real life. Please do not take anything in this post or any other post on this blog as medical advice. If you have questions or concerns of your own, please seek advice from your doctor.*
Labels:
CGMS,
Dexcom,
Diabetes,
ITP,
Rough nights,
T1 Diabetes,
The Superhero
Saturday, June 4, 2011
The Princess and Her Shoes
As I was searching for a pair of sandals in "the basket" the other day, it occurred to me that The Princess has A LOT of shoes.
Back in 2009 I posted HERE about The Princess getting new shoes. That specific time shopping, we ended up with 6 pairs of shoes. And I thought that was a lot.
Her latest collection of "current" shoes (shoes that fit her NOW), is MUCH larger.
So as I was looking for that pair of sandals the other day, I decided to line up her shoes and count how many pairs she has, and of course to take a picture to share here on the blog.
To my surprise, this 2 YEAR OLD has SIXTEEN (16) pairs of CURRENT shoes! (2 not pictured, flip flops)
And with THAT I would like to say two things...
1) Yes, she really wears ALL of them at one time or another.
2) I did NOT buy her all of these shoes. She is lucky to have a shoe obsessed NaNa who helped this collection grow. :-)
Love little shoes!
ETA: After reviewing the shoe photo, I decided to label each pair with who bought them. Maybe I am more shoe obsessed than her NaNa?
This pic below is labeled, it does not include 2 current pairs I couldn't find the match to last night. I also have 2 pairs up in the closet for when she grows a bit. :)
Tally: 1 Aunt Tricia, 5 NaNa, 1 Formerly The Superhero's (maybe NaNa?), and 9 Mommy!
*Disclaimer: I am a mom of a T1 Diabetic child and a child with ITP/Asthma/Dysphagia. I am NOT a doctor. I just play one in real life. Please do not take anything in this post or any other post on this blog as medical advice. If you have questions or concerns of your own, please seek advice from your doctor.*
Back in 2009 I posted HERE about The Princess getting new shoes. That specific time shopping, we ended up with 6 pairs of shoes. And I thought that was a lot.
Her latest collection of "current" shoes (shoes that fit her NOW), is MUCH larger.
So as I was looking for that pair of sandals the other day, I decided to line up her shoes and count how many pairs she has, and of course to take a picture to share here on the blog.
To my surprise, this 2 YEAR OLD has SIXTEEN (16) pairs of CURRENT shoes! (2 not pictured, flip flops)
W.O.W.!!!!
And with THAT I would like to say two things...
1) Yes, she really wears ALL of them at one time or another.
2) I did NOT buy her all of these shoes. She is lucky to have a shoe obsessed NaNa who helped this collection grow. :-)
Love little shoes!
ETA: After reviewing the shoe photo, I decided to label each pair with who bought them. Maybe I am more shoe obsessed than her NaNa?
This pic below is labeled, it does not include 2 current pairs I couldn't find the match to last night. I also have 2 pairs up in the closet for when she grows a bit. :)
Tally: 1 Aunt Tricia, 5 NaNa, 1 Formerly The Superhero's (maybe NaNa?), and 9 Mommy!
*Disclaimer: I am a mom of a T1 Diabetic child and a child with ITP/Asthma/Dysphagia. I am NOT a doctor. I just play one in real life. Please do not take anything in this post or any other post on this blog as medical advice. If you have questions or concerns of your own, please seek advice from your doctor.*
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