Selket
Been there - done that
- Joined
- Feb 28, 2000
- Messages
- 4,853
OP here - for now we're going to put off any plans to go to WDW because of the newness of this all and trying to figure out what is best for DS. One person here mentioned that a DAS actually makes things worse for her because of more walking and more sun, and I just want to clear something up that we didn't know either until this weekend. We assumed that more activity and being in the sun and heat would cause lows. It turns out that this doesn't happen for everyone. DS was camping with his Scout troop and even with not having much shade (came home with a little sunburn on his neck) and all the camping activities, his lowest blood check was 90. Now today it's raining and he's at school and there's no outside recess. The school nurse called me at noon because he dropped to 53 and needed juice to recover. So I'm learning that not everyone's needs are the same. I'm finding that DS needs to eat on schedule or he starts to crash but my friend's daughter can eat dinner at 9 pm and she's fine.
I was away on vacation so I didn't see this until yesterday. I think you've hit the nail on the head - that not everyone's needs are the same. My son was dx'd at such an early age that we've had to deal with toddler through teen. There are many times when I swear I could do the same thing twice and get completely different results. When he was first diagnosed we really had to stick with a more rigid meal plan and eating times and many other things and this fortunately got easier over time. There's such a range of treatments (from older insulins like NPH and regular up to new ones like Apidra) and some are on shots, some pumps, some also have a continuous glucose monitor - and I also think the body responds differently depending on hormones and so on - there's no one size fits all when it comes to this disease. He may also be on the "honeymoon" phase (they used to call it this anyway) where the body is still making some insulin - which doesn't always make it easier to figure out how to bolus for food and basal...but it could me that his needs may change over the next few months to a year. When my son was dx's he didn't need any overnight basal insulin for a few months - but then his numbers slowly started creeping up. We also had to use diluted insulin because his bolus needs were so small - a half a unit could bring him down way way too much. Of course now as a teenager it's quite the opposite (he needs more insulin than he may as an adult). Best to him and you and your family and hopefully you can fit the Disney trip in when things settle down some. Feel free to PM me anytime!
