Hello everyone. I was wondering if any of you check your children's bs at night to see if they experience any lows while they sleep. My sons Endo suggests at every appointment that we check him for a few nights around 3am. Well it usually ends up he's fine. I was told by some type 1 friends that if his bed is soaked from him sweating it's because he went low during the night and his body reacted to raise his bs level . He has woken up like that but not a lot. This week he ended up being low 1 night. I checked him at 3am the first night and he was in range but he woke up higher than when I checked him at 3am which has me thinking he may have went low after I checked him and his liver produced some sugar. The following night I checked him at 4am as I figured 3am was to early too catch the low. Well he was 3.3, so an oj juicebox was given and I checked him again just before 5am and he was good. I will probaly check him every night now as I won't be able to sleep due to worrying if he's dropping in his sleep. Losing sleep is a sacrifice I can make. And yes he gets a bedtime snack before he goes to bed. So much for being well rested to got to work LOL!. Oh well, work sucks but that is another topic I will talk about later.
If anyone else experiences the same thing with their kids and have found ways to avoid the nighttime lows let me know.

Views: 9

Replies to This Discussion

Thank you all of you for your insight and stories and wonderful advice. The protein before bed is great and helps our son throughout the night. We still occasionally check him but normally it's only if we have a feeling that he needs to be checked. Since I do not work shift work anymore and have settled in to a new job it has been more of a challenge to get up and check him but my wife has it pretty well nailed down for his snacks before bed and we have not run into too many lows. We make sure he has a glass of milk every night with his snack before bed and we also keep a baby monitor beside him to listen to him and keep us at ease a bit. I still go through some sleepless nites and weeks but I feel better knowing what his levels are and I eventually get my sleep back, lol.
I am glad to see I am not the only one worrying, I worry more than my wife does but we have been dealing with it so far. I am glad to say he has been healthier since he had tubes put in his ears in July and I pray that means a good winter this year compared to last. We are used to him having back to back colds all year and no real break from being sick. Since the tubes he has been cold free which is fantastic but his asthma seems to have gotten worse a bit this fall. I swear we're a travelling drugstore when we go out. Lol. Anyways, he has started JK this year and so far so good. No real issues with the teacher other than making her understand his D and putting emphasis on communication between all of us. The one thing I put my foot down on was we were unaware he had another teacher who we had not spoken or met with to discuss his diabetes. She also would not let him eat his snack in the library or computer room! She would make him go to the office to eat it, not what we wanted to hear. He felt like he was being punished for having to go to the office. One of the things we stressed to his teacher was that he not be singled out or made to feel different because of his diabetes. Let his friends watch when he gets his finger checked and when they question why he is having a snack tell them why, don't hide his D, they will be the ones that will be looking after him as they grow up together and they should know all they can to help him. This is no longer an issue according to the principal who has been helpful in making this an easy transition for us. We eventually want to meet all staff as he gets older so that the more people who know about him and look after him the better.

I noticed a few other questions about daycare and such, please feel free to ask my wife or I anything. Our son has been in daycare cince he was a year old and only missed 6 months after he was diagnosed. We found a great daycare, which happens to be inside his current school, and the people there are fantastic. We had the local diabetes association (it was a challenge getting them to go) meet with them as well as us showing them how to work his meter and explaining what to look for in signs of lows or high and how to treat them. We are 100% confident in the workers there that look after him. School will take a bit more work as this is new ground for them. Unforunately, the area here is very "diabetes dumb" to put it bluntly. This also includes some healthcare workers as well, but that is another discussion.
Thank you again and if you have anymore suggestions please let us know.
I check my son at least twice during the night, maybe more depending on what his sugar is when I check it. I'll give you the main reason why. When I checked him at 4 this morning his sugar was 50.
I feel your pain! This can happen even with tested basals. We are 3 and a half years in and her lows are more erratic than earlier in dx, can't pinpoint a specific reason all the time. Also, where she always used to come up with juice or glucose tabs, it now sometimes takes more than one treatment to bring blood sugar back up.
my son was just diagnosed 3 weeks ago today and i was told not to check him at night time but since my son has autism and does not speak i do check him more often in the day time because i dont know when he is low or high

RSS

Advertisement



REsources

From the Diabetes Hands Foundation blog...

Together, We Can Get Diabetes Co-Stars to 10,000 Views!

Above is a photo of Diabetes Hands Foundation’s own Manny Hernandez with the stars of the Diabetes Co-Stars Video, “Strength in Numbers.” In case you haven’t heard the news yet, there is a new video making it’s way through the …
Continue Reading

Congratulations Diabetes Advocates Scholarship Recipients!

The Diabetes Hands Foundation and Diabetes Advocates Program is proud to announce and congratulate the members of DA who were granted scholarships to attend diabetes conferences in 2013! Thanks to a generous grant from Novo Nordisk, in 2013 we were …
Continue Reading

TuDiabetes Team

DHF STAFF

Manny Hernandez
(Co-Founder, Editor, has LADA)

Emily Coles
(Head of Communities, has type 1)

Emily Walton
(Business Manager)

Mike Lawson
(Head of Experience, has type 1)

Corinna Cornejo
(Development Manager, has type 2)

Heather Gabel
(Administrative and Programs Assistant, has type 1)

DHF VOLUNTEERS


Lead Administrator
Bradford (has type 1)

Administrators
Lorraine (mother of type 1)
Marie B (has type 1)

Teena (has type 2)

Brian (bsc) (has type 2)

jrtpup (has type 1)

 

LIKE us on Facebook

Spread the word

Loading…

This website is certified by Health On the Net Foundation. Click to verify. This site complies with the HONcode standard for trustworthy health information: verify here.

© 2013   A community of people touched by diabetes, run by the Diabetes Hands Foundation.

Badges  |  Contact Us  |  Terms of Service