Showing posts with label parenting a child with type 1 diabetes. Show all posts
Showing posts with label parenting a child with type 1 diabetes. Show all posts

Thursday, January 16, 2014

3 Tips for Parents of newly diagnosed Children with Diabetes

I was recently asked what advice I would give a parent of a child newly diagnosed with Type 1 Diabetes. It has been a number of years since I fell into that category but I can sadly remember it all like it was yesterday.  That being said, it was an easy question to answer and comes in the form of three pieces of advice.
 
First and foremost, live your life four hours at a time.  Do not worry about six hours from now. Do not worry about tomorrow.  Live life in four hour time slots--nothing more.
 
Chances are high that your child is using a rapid acting insulin. They basically last four hours.  Look at readings inside the four hour window.  Look at food and activity in that four hour period.  If you see a reading that is in range for that four hour period give yourself a high-five! You did fabulously! If you see something out of range during that four hours then begin to problem solve.  What can you learn? Did you learn that your child is producing a small amount of insulin now and doesn't need as much insulin for that food at the moment? Did you learn that not all slices of bread are the same number of carbohydrates? Did you learn that hockey practice before supper changes the amount of food and insulin your child needs?
 
Four hours. Its simple. Its manageable...and for an overloaded parental mind, really it is more than enough to handle.
 
My second piece of advice is to find a support system and use it! Let parents, partners, friends, and people from support groups (online and in real life) help! Share with them, unload on them, and again...use them.  Some people will "get it" more than others and that is okay but find a way to lean on even those who may not get it but are willing to learn, listen or take over for even an hour.  You deserve the break.  You cannot be the very best external pancreas that you can be without a break and an outlet.  Its okay to ask for help or even see a counselor. Many families with diabetes have to turn to someone along the way.  Its okay to do this.
 
Finally, cry in the shower.  Go ahead! Stand in that shower and let it all out. Let go of the big girl/boy pants, crumble and let that strong shell crack for just a little while.  Allow yourself to feel the pain and frustration that comes from a diagnosis of diabetes for your child. Allow yourself to feel the anger and hurt.  Allow yourself to grieve while the water washes away a bit of the pain so that you can be strong again once you step back into the real world.
 
You can do this.  There will be bumps.  There will be victories.  The landscape of your life, and that of your child, has changed forever.  This doesn't mean that he/she will never achieve their dreams or live a long and full life.  It means that your perspective will shift a little (or maybe a lot). You will find new friendships that will bring you through the worst of times and celebrate with you in the best of times.  Life will be different but it can still be amazing...just four hours at a time.
crying in shower

Tuesday, June 4, 2013

Its a BAD day for Da 'Beetus

"Mom you should have warned me!"
What was he talking about?
"Mom you should have warned me that we have a clinic appointment tomorrow! I would have done a lot better. Today was a really bad day for da 'beetus!"
He did know that he had a clinic appointment today. He simply chose to forget...like he forgot to test a number of key times throughout the day and like he forgot to bolus for his supper! It was a very bad day for "da beetus" alright!
I have downloaded his meter. I have written out his basal patterns and the result is that I don't want to know what his A1c is because I know it will be bad.  I also wonder what I have been thinking in looking at his basal patterns on the weekend versus the weekdays.  The weekdays are a mess. My first guilty thought was "its time to do some serious basal testing and fix this!"  My second thought was "why?"  This is my son's last full week of school.  Next week is an exam every morning and then slacking...I mean studying every afternoon. After that it is basically summer vacation, a time when we switch over to a permanent "weekend" basal pattern.
I hate the thought of our team looking at his readings. They are a mess but each one tells a story.  They say... "He didn't weigh his cereal."  "He eats constantly and there is no break to test basal patterns."  "He is working out and we are working at learning how exercise impacts his insulin needs."  "Mom has given up asking for data and works with the little information that she gets."
My son said that I should just let our team do their job. That would be great but they have no data either! How do you say adjust that basal or bolus ratio based on a reading that was taken 20 minutes AFTER he ate? Hopefully they will simply be on board with helping to get us a CGM in the fall or whenever the DexCom comes to market.  Perhaps they they will remind him to test if he wants his licence.
I hate clinic appointments. Why do they always feel like you are going into the principal's even though you know that you are doing your very best? Perhaps I will just go in, keep quiet and let my son handle all of this one...that would make things interesting! Wish us luck!
kid diabetes