Showing posts with label Insulin. Show all posts
Showing posts with label Insulin. Show all posts
Tuesday, January 31, 2017
The 'What If' Game
5:51 PM
Posted from Facebook 1/20/17
After almost 8 years with Type One Diabetes we have learned to roll with most anything it throws our way. Some days are easier than others and some days are much harder.
Last night while Nate slept his blood sugar dropped unexpectedly. Those little red dots are sever hypoglycemia that he slept through and we almost missed. By the time his Continuous Glucose Monitor alarmed, his blood sugar was 47. I fear it had actually gone much lower but by the time we got to him his body had already started fighting the hypo, thankfully.
His liver dumped glucose (its much more complicated - won't go into it all here) which saved his life. We gave him 10g of carbohydrates which would normally raise his blood sugar by about 100 but his blood sugar soared over 500 and stayed there most of the night.
It was a long night filled with what-ifs, what could have beens, and FUD. I share this not looking
for sympathy or praises but instead to educate.
for sympathy or praises but instead to educate.
Diabetes is not a joke, it's not a punchline, and it's not to be taken lightly.
I don't exaggerate when I write this ---
We could have lost him last night. While he slept. In the next room.
I can't even think about it without tears stinging my eyes and rolling down my cheeks --- it makes my body physically ache to go over what could have happened. And I went over it in my head all night long.
There's nothing funny about that.
And I'm not alone. There were moms and dads around the world carefully watching over their children last night. Forcing them to eat in their sleep to keep them alive, carefully calculating insulin doses to lower dangerously high blood sugars, and some just watching the rise and fall of their children's chest because sometimes the fear is so overwhelming.
There were adults doing it all too. These babies grow up and diabetes doesn't go away! Wives checking husbands, husbands battling with hypoglycemic wives ...
❤️

It's a tough disease and the people that live with it are amongst the strongest people I know! They are warriors.
--- Thankfully smooching Nate's face off this morning while he rolls his eyes, grins his silly grin, and allows me to love on him all while he has no idea what happened last night. 

❤️

Tuesday, May 8, 2012
Insulin Overload --- what could have been a fatal mistake
6:52 AM
in·su·lin/ˈinsÉ™lÉ™n/
Noun: |
|
Insulin . . . such an important part of my life today. The small vial of insulin that I pick up at my local CVS pharmacy each month literally keeps my son, Nate alive each day. Without his insulin pump, the OmniPod infusing insulin into his body 24 hours a day/7 days a week Nate would not be able to live.
I've said it many times the scariest part of Nate's T1 is that the very same insulin that keeps him alive and healthy can actually cause extreme hypoglycemia which could lead to a coma, brain damage or death. It's a very, very fine line.
The insulin isn't magic and Nate's pump isn't magic . . . although that would be really nice. Jim and I have to calculate each dose of insulin that Nate receives through his pump. It is a non-stop, never-ending, always-changing job that keeps us on our toes at all times.
Mistakes are not an option when it comes to insulin.
That being said . . . Saturday the 5th of May, 2012 a monumental mistake was made and it could have been fatal. I'm not saying this to be dramatic ---- it is a fact! If we had not realized what we had done --- the mistake that was made ---- it would have been fatal.
Most of my readers know that Jim and I are going through a divorce, he works out of state most of the time and I handle most of Nate's diabetes care. Jim can do everything that I can do --- he's just not here most of the time so the every day ins and outs of D care are mine. Nate has been pumping with the OmniPod for over 2 years now and I can probably count on one hand the number of insulin injections I've had to give Nate from a syringe. In that same time Jim has not had to give Nate any injections via syringe.
So, Saturday was a rare day for us. Jim was in town, it was his weekend with the littles but he had a ton of work to do so I volunteered to hang around and help out so he could get it all done. Yea . . . pretty much I had nothing else to do all weekend so you know --- I was nice. :)
I decided to take the kids hiking Saturday afternoon and at the last minute Jim decided to take a break from work and tag along. I was actually happy he decided to go. As much as I love hiking with the littles --- it can be a bit challenging solo.
As we were hiking Nate's pod fell off and being the stellar D Mama that I am I didn't have another one with me (I always have an extra or 2 with me EXCEPT for when I actually need one). I wasn't worried at all during the hike because he stays in range with the help of a lot of carbo boosting along the way. After our very long, hot and dirty hike we decided to grab a bite to eat and instead of doing a pod change we decided to just give Nate an injection to bolus for dinner. No. Big. Deal. Except it turned out to be a VERY. BIG. DEAL.
We SWAGGED dinner and decided that Nate needed about 1.25 units of insulin. Jim drew up the insulin and was handling giving Nate the injection while I took the girls to the restroom. As I was leaving the table I could tell that Nate wasn't too thrilled about a shot so I decided to grab the syringe and give the shot in Nate's arm really fast while Jim was distracting him. I never even looked at the syringe just picked it up, stuck it in, and pushed down on the plunger. As soon as I did I knew something was very, very wrong. I asked Jim how much insulin he put in the syringe and he very confidently answered 1.25 units. I asked him to show me on the syringe because I knew . . . I knew by the feel that I had never given that much insulin before. When he showed me on the syringe he pointed somewhere between the 10 unit line and the 15 unit line and my knees went weak. He thought the 10 was 1.0 and the 15 was 1.5.
I actually felt the blood drain from my face and I saw the look of absolute fear in Jim's eyes when I told him what we had done.
We gave Nate 12 units of FAST ACTING APIDRA.
To date Nate's largest bolus has been 4 units and that made him bottom out. His current total daily insulin intake is around 11 units per day. 12 units of fast acting insulin in my 3 year old son was a fatal dose and we kind of freaked the F out.
The part that scared us both the most is that if I had not decided to turn around and help with the shot Jim would have never known that he gave Nate 12 units of fast acting insulin. The what ifs and the what could have beens were pretty overwhelming.
I usually handle all things diabetes pretty calmly --- I avoid the hospital like the plague when it comes to Nate and diabetes. I'm pretty cocky . . . always thinking ---- I got this. This time I was ready to go straight to the ER --- I was pretty scared. I stayed calm and Jim and I very calmly and quietly discussed our options. We were soon overwhelmed when we realized Nate's dinner time insulin to carb ration (I:C) is 1:30. That means he only gets 1 unit of insulin for 30g of carbs eaten. That meant we need to feed Nate 360 grams of carbs to keep him safe. CRAP! I did call the on call endo at Children's but she said 'just give him some ice cream' . . . ummmmmmm ok!
Jim and I decided we could handle it and it would be more traumatic for Nate if we took him to ER for glucose drip. So, we began the carbo overload right there at Uncle Julios! We started with regular Coke --- 2 glasses, ordered sopapillas with extra honey & ice cream. When we left the restaurant we stopped and picked up a few treats . . .
Jim kept up with carbs on paper and I kept up with my iPhone calculator.
I kept adding to my calculator each time we convinced Nate to eat something else. I like this picture because if you look closely at the top you can see a message from Lexi was coming in to check on me. I absolutely loved the way the D moms and dads, family and friends rallied around us Saturday night. Every text message, phone call and FB message seriously kept us going and kept us encouraged enough to know that we would be able to get through one of the scariest nights of our lives.
And no . . . Nate didn't eat GaGa . . . she brought cookies and treat over for him to eat so I guess instead of writing all of those things down he just wrote GaGa. :)
Nate's blood sugar hovered between 90 and 159 all evening. It would drop, we would feed, drop and feed, drop and feed. We ended up finally giving 270g of carbs and 2 mini glucagon (4 units each) and he never dropped below 90 not even when the Apidra peaked.
When we finally saw his bg rising later that night we put a pod on and started his basal again. He ended up pretty high after the pod change but after the long night that we had . . . I was so ok with it!
Oh yea - - - did I mention that 270g of carbs had Nate bouncing off the walls? He was CrAzY!
As per usual all pics were taken with my iPhone so please excuse the terrible color and all that blah blah blah!
Nate was in carb heaven . . . he and the girls never knew the severity of the situation or really that there was a situation at all. They just enjoyed munching on candy, coke and ice cream all night.
We kept calm and carbed on!

Labels:Apidra,Diabetes,Insulin,Insulin Overdose | 19
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Just a Mom
I am NOT a doctor, nor do I play one on this blog.
I AM a wife.
I AM the mom of 3 wonderful children.
I AM my son's pancreas.
The information provided on this blog is from our personal experiences with Type 1 diabetes. Because something works for us does not mean it will work for you.
Please consult your doctor if you have any questions or concerns about your health care options.
I AM a wife.
I AM the mom of 3 wonderful children.
I AM my son's pancreas.
The information provided on this blog is from our personal experiences with Type 1 diabetes. Because something works for us does not mean it will work for you.
Please consult your doctor if you have any questions or concerns about your health care options.
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