I am frustrated with myself after reading my son's blood sugar levels. WHY DO THEY GET SO LOW AND SO QUICK? I get him where he needs to be, he eats great and then later on he will go well below 100. His target blood sugar level being a T1 kid is 100-180. At school he has been getting 76 before lunch. UGH! That is way too low. He goes to the nurse a minimum of twice a day to regulate this. She gives him correction in Milk or another snack we provided that has 15grams of carbs and then he is back where he needs to be. Ready and focused to learn and make new friends, and for that I am extremely thankful for.
Having a hard time not beating myself up about this... but I am. Last night after taking his blood sugar I started sobbing. Why was he at a 86? I have tried very hard to show him how strong we can be with this new life change, but again he needs to see that his mommy is human and everyone has the right to express how they feel.
He ate dinner an hour before AND even had a snack in between and had an amazing reading. Then right at 8:00pm, when he was scheduled to take his night time insulin Lantus, he was way too low for me to administer. I then called his nurse and she told me to just keep rotating in every 15 minutes with correction of 15g of carbs to help him get back up. After 30 minutes he got back to 145 and was ready to go to bed. But, I still was upset with it. Upset that I did not notice he was getting low. I am thinking more snacks will help with this??? For his blood sugar readings we use Accu-Chek Blood Sugar meter. I am very happy with it and we chose a cute and fun basketball decal on the face.There is a program where it stores the time and the reading. Love that feature since being a mom it maybe hard to write down the reading every time. But with this feature I can dedicate my time to go through the screen and write down in his log book.
He is officially in the
Honeymoon phase of his diabetes. This is where the insulin actually communicates with his pancreas and it starts producing it's own insulin on it's own. But.. unfortunately it is only temporary and can last up to two years. So regulation is difficult during this time since levels fluctuate so often. Wished there was this magic pill he could take that would send a message in code to the pancreas and tell it to work for life. Or just transfer it's laziness over to my pancreas and allow his to have the power and energy mine has in insulin creation. I am 30 years old and experienced that whole LET'S EAT WHATEVER I WANT AND NOT THINK TWICE ABOUT IT. He doesn't get that anymore... and I am beyond pissed about it.
{Deep breath in.}
I am very anxious to go to his first doctor's appointment on Friday. It is at Cook's Children's and will always be until he is 18 years of age. I am looking forward to talk more in depth about his nutrition. Look forward to any suggestions from the doctor. Then next month I have a training/nutrition class that is 5 hours long. I am beyond estatic to attend this one. It is all about the disease, correction, and learning how to live with T1. Plus, I will be honest. I am going to make friends with everyone in the class. I'll ask around and see if anyone lives close to us. If so, this will be the start of a group of family and kids that all can grow and learn from one another. I need a sense of community in all of this. So far the closest T1 community is a bit too far for us.
One top of my priority list and always will be... how to feed my whole family a healthy and balanced meal without lacking in taste or insulin calculations.
May the force be with me!
Much love and laughter,
Nush
P.S. Tomorrow I'll be posting a very cool giveaway! Come back tomorrow to check it out.