Published Mar 30, 2010
Keepstanding, ASN, RN
1,600 Posts
lots of paperwork, lots of questions and really keeps me on my toes !
i am always a little nervous when i recieve a new student with diabetes. insulin dependent, fragile, young.........
hope i am not alone in my nervousness !!
praiser :redbeathe
DistrictNurse19
66 Posts
No, you are not alone! A newly diagnosed diabetic who is in the "honeymoon" stage is enough to make your B/P rise big time as their blood sugars ride the crazy rollercoaster all day long!! It is best to have a plan in place, written preferably by the healthcare provider (pediatric endocrinologist) that will address the target range of blood sugars as well as the dosage/time of insulin and the number/time of carbs. If I don't have a plan spelled out, I get real nervous!!
no, you are not alone! a newly diagnosed diabetic who is in the "honeymoon" stage is enough to make your b/p rise big time as their blood sugars ride the crazy rollercoaster all day long!! it is best to have a plan in place, written preferably by the healthcare provider (pediatric endocrinologist) that will address the target range of blood sugars as well as the dosage/time of insulin and the number/time of carbs. if i don't have a plan spelled out, i get real nervous!!
i totally agree district thanks for your input.
praiser:redbeathe
luvschoolnursing, LPN
651 Posts
Especially tricky for you, Praiser because aren't you in elementary? I had a new one diagnosed over Christmas break but he is 15. Not that it is without challenges. Adolescents have their own set of problems not just with learning the routine but accepting the diagnosis. (No-if you ignore it it WON'T go away) Somehow the little ones are scarier, though. You'll do a great job!
mustlovepoodles, RN
1,041 Posts
I have 2 relatively new diabetics in my elementary school. The 5yo has been diabetic for a year and the 9yo has been diagosed about 8 months. The older one was always high until she got her pump 2 months ago. Now her sugars are in tight control and I hardly have to do anything but help her count carbs(and she's getting better that that.) Its the 5yo that gives me a fit. She is very brittle. She can come in at 8:15 at 341 and before 10:30 she's 54. Then lunch brings her up, but by 2pm she's often crashing. Four times last week! and bless her heart, she is just about clueless. Thankfully, she *does* recognize when she's low, and she's never wrong. Still, it makes me a nervous wreck.
BunnyBunnyBSNRN, ASN, BSN
995 Posts
Praiser,
You are not alone! {{{HUGS}}} New dx anything is enough to make any one of us a nervous wreck.
SchoolNurseBSN
381 Posts
You are not alone! This is a prime example of why nurses are so needed full time on every campus. If it makes us nervous, what about the unlicensed people that have to help these kids?
kidsnurse1969
86 Posts
When you stop getting "flutters" in your gut then it might be time to get out of the business.:redpinkhe
rph3664
1,714 Posts
Adolescents have their own set of problems not just with learning the routine but accepting the diagnosis. (No-if you ignore it it WON'T go away)
And for middle-aged Type IIs, eating candy by the pound, smoking, defiantly refusing to take your medicine, etc. won't make it go away either. It can definitely make your eyesight, legs, kidney function, etc. go away, along with the rest of your body eventually.
This isn't just something that kids do.
momof4nurse
5 Posts
I agree nurses are needed in the schools. Having worked in the hospitals I've seen the longterm damages diabetes have on the body. Its sad and depressing knowing much of that could have been avoided of patients had better understanding of their disease and how to manage it. School nurses have a great opportunity to help these kids succeed, make better decisions and live healthier lives. Hopefully we won't see them in the hospitals with diabetes related complications in the future.
Praiser, the parents of that child is fortunate to have you there to care for their child. Keep up the good work.
frann
251 Posts
There's a really good support group for the parents
over at
CWD-childrenwithdiabetes.com
they're my other family there-as my dd was dx almost 5 yrs ago now. Its a life changing experience.
another good resource is type1parents.org
I don't go there anymore just due to time, but they have info really well organized