This patient support community is for questions related to juvenile diabetes including
Celiac disease,
depression, diabetic complications, hyperglycemia /
diabetic keto-acidosis,
hypoglycemia, islet cell transplantation,
nutrition, parenting a diabetic child, pregnancy, pump therapy, school issues, and teens with
diabetes.
I've read "somewhere" that our urine should be nearly colorless with jsut a bit of yellow; darker yellow means we're not well-enough hydrated. I use that rule of thumb myself, but do check it out with your child's doc.
Perhaps others will post with good info to share, too.
While we'd normally expect to see adverse symptoms during the high or low, itself, perhaps it's the total accumulatoin of all that that causes the symptoms in the aftermath.
I'm glad to hear things have levelled out with the pump. **Thank you** for taking time to share your insights here!
Hello - I am the parent of a 9 y.o. with diabetes (originally said to be type 1 but now they are looking into MODY). Our daughter is not Celiac -
She has a very high pain tolerance but has had intermitent bouts with stomach pain over the past year and a half - which is when her diabetes started.
OUR pediatrician and endocrine both state that they "don't think her stomach pain is related to her diabetes" - I know it is - she NEVER had this pain especially this often before her diabetes.
I can say that we have gotten to a point of nearly ZERO stomach aches and pains by either removing or significantly reducing her intake of dairy (milk and cheese), processed foods, high wheat foods and complex carbs (bread, pasta, white rice etc). We also increased her intake of fresh fruits, veggies and natural foods. And added a fiber supplement (benefiber) just to help her body with digestion and processing what she does eat. Her body did not have any problems diagesting the foods that she struggles with now before her diabetes.
The pancreas has multiple functions in that it produces and secretes hormones (including insulin) and digestive enzymes necessary to break down carbs, protein and fat.
I actually found this website just this evening looking for some type of study about the pancreas and its' other functions and how it could affect a person with insulin dependent diabetes.....
We are 100% sure that this has helped our daughter - but I am determined to find a study or something to help substantiate our findings so that I can forward that information to other parents that deal with our same frustrations.
It is such a powerless feeling to just watch my daughter in pain. We are new to diabetes (11 months) but we have always been a very nutritionally conscious family.
By keeping her diet clean and simple - we have made a huge difference in our daughters stomach aches.
If we all keep reaching out to one another and working toward gaining more knowledge and empowering ourselves - hopefully we can figure this out so that our children don't have to suffer......as KManis stated above - It is diffucult enough to see your child suffer with diabetes.
We took her to the pediatrician and they did an X ray of her stomach area and a blood test to test her pancrease to rule out pancreatitus (pancreatitis). They also tested for bacteria in her stomach/blood stream. All tests came back normal. He put her on Prevacid.
So we kept track of her blood sugar, keytones and food eaten. I did this for a week and then called her Endocrinologist. I faxed them the log and they said that they didn't feel it was diabetes related and told us to go back to her pediatrician and have him do a Celiac test.
We went back in to see her doctor and he took some more blood to do the Celiac test. While at the doctors she seemed in no pain. This happened all of the time. No one seemed to be witnessing the pain she gets in so it seemed that no one belives us. The pediatrician increased her Prevacid to 2 pills a day. I had tried Prevacid for a week now with no change in the pain. I tried Tums and Peptobismo. Neither helped the pain. I tried childrens Tylenol (doesn't help). I also tried Hydrocodone (she had this from when she broke her leg) and it didn't phase the pain and infact she said it made it worse.
So when we were leaving her doctors after the blood test for the Celiac, she doubled over in pain. She was getting in the car and had just shut the door and was screaming. I thought that she had shut her hand in the door. When she could finally talk she said it was her stomach. Of course I was panicking and was going to rush her to the hospital. I thought it may be her appendix. It ended up subsiding so I took her home but she was very lathargic and wouldn't eat. We took her to the childrens hospital that night.
They did a blood test and a CT Scan and tested for all kinds of things. All came back normal. While we were there the pain was gone. So all the doctors saw was a little girl with nothing wrong with her. It's been very frustrating. They ended up saying that her bowels were slightly impacted (but she was always having daily bowel movements). So they gave her an enima and sent us home. So we still have no answers after all of this.
We started exploring the posibility that it was in her head and possibly stress related to school. Although we noted that over the holiday while she was out of school it continues to happen. So that kind of discounts that. Her blood sugar has been high for no reason. I'm going to start watching for it to go high then bottom out and then get normal and see if that is when the pain happens. She has had some keytones but not consistant.
She's back at school and having less pain but she went through about 2 days of no pain and then it was back at one point. So I'm not confident that this is over. Nothing helps the pain at all. If we could just at least get her some relief from the pain, that would be better then nothing since no one can figure this out. It's bad enough that she has to got through shots and finger pricks but now stomach pain. What more could a 6 year old go through. I just am so frustrated and concerned.
We feel so alone but reading everyone's emails make me feel slightly better. At least we are pretty sure that this ISN'T all in her head. What's hard is the lack of help we got from her diabetes team. The doctor is really, really good but very busy and didn't provide much help to us. I would think that he'd be familiar with the stomach pain related to diabetes. Reading all of this sounds like there are lots of people going through this. Surely someone has figured this out.
Meanwhile, our tiny daughter is in pain and we are attempting to get her mind off of things and get her back in school so that she's not behind and left out of life with friends and class mates during the holidays. She seems to be a little better but what the heck caused all of this???!!!
What I'm wondering is if this might have anything to do with her pancrease finally shutting down completely. We've been in the "honeymoon" period all this time and with the blood sugars going high for no reason, I'm wondering if possibly the stomach pain is related to the extrem highs then lows and the hights might be caused by her pancrease completely shutting down. We have started increasing the insulin over the past 2 weeks but are going slow since shes so young. Don't want an extreme low in the middle of the night. It's happened a few times and she hasn't woke up every time.
I'm just frustrated that we're having to diagnose this all by ourselves. Good luck everyone who is going through this same thing. My heart goes out to you and your kids!