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RE: [IPk] Help or advice before I totally crack up
Hi Jos and Bev
I do go along with Jos and think there is so much more these days that we have
know about treating
diabetes. My best friend at school started off on one injection a day,and the
whole time I was at school
with her (and when I was at her house which was quite often, I never once saw
her go or have a hypo. I
think Drs then were more interested in stopping hypos that preventing high
blood sugars. I have a very
old book for parents of children with diabetes that was withdrawn from the
library some years ago. I
bought it at a library sale out of curiosity. It makes very odd reading
compared to the things we or our
children are expected to do these days. The best thing was, from my point of
view was that people were
taught to calculate portions then instead of the vague "eat a healthy diet"
with no guidance at all how
to match carbs and insulin.
Sasha hasn't been allowed to go on a sleepover as like Jos's daughter she has
never had any hypo
awareness at night and has had about 6 or 7 seizures during the first two years
of D. We have to get up
every night and test about 2.30am. When she is older and maybe has a cell phone
I can ring her and get
her to check or make sure that she has less insulin. Although Beckie has been
asked to a couple of sleep
overs no one has asked Sasha. She has only recently begun to do her own
I think I would be worried just as much if a child was using a pump, as Jos
said, the site could fail, or
Danielle might misjudge the amount to bolus, or bolus too much, or two close to
another bolus so its all
The only thing is that in a few years time the children will be more able and
confident to take the D
care with fewer mistakes. (one hopes)!!
I do try to let Sasha do most things that the other children do. There arent
many things I say no to.
Sleepovers are one of them at the moment and she has not really made a fuss
about it. You couldnt expect
someone elses parents to get up and test in the middle of the night.
We also have the coeliac problem to deal with too. So the twins have to take
their own food
everywhere!!! Its all so much hassle sometimes!!!
Jackie,Mum of Sasha aged 8 dx 1999, twin sister Rebecca, both coeliac 2001
Mum also to Danni and Nicola, wife to Terry
> -----Original Message-----
> From: email @ redacted [mailto:email @ redacted]On
> Behalf Of J
> Sent: 04 May 2003 11:37
> To: 'email @ redacted'
> Subject: RE: [IPk] Help or advice before I totally crack up
> On 4 May 2003 at 9:31, Smith, Beverley wrote:
> > I would not want them to take the
> > risks I took (never testing my blood, always eating sweets
> > etc) but perhaps I am a much stronger, independent person
> > for having worked all that out for myslef?
> Hi Beverley,
> Do you think that todays ideas of tight control and the
> resulting higher chances of hypos change things though? The
> pump also gives less time and more potential for DKA if
> handled incorrectly. The high BG's experienced by Barbara's
> daughter *could* have been a sign that her site had failed
> and presumably DKA would be well advanced if she had gone
> to bed in that situation?
> I do try and let my children do as much as they would have
> done if they didn't have diabetes. My 12 year old son is
> currently staying with friends on the other side of the
> country. However, it wasn't such a difficult choice with
> him as he is still in the honeymoon phase and on very small
> doses (10 units am, 4 units pm). I think I would need to
> think much harder about Emily going as her diabetes seems
> much more volatile. I would probably aim for her BG's to
> run a little high for the week but even then she would
> probably have hypos. She does her own blood tests and
> injections, knows how to treat hypos and is beginning to
> take an interest in the carb counting side. But, there
> seems to be so much to take into consideration when working
> out the dose, carb value of meal, type of food (she needs
> her injection after her meal if it's pasta), exercise, how
> much to deduct if it's close to the last injection and add
> to correct high BG's. It's a lot for a 10 year old to cope
> with. I would have to work it out over the phone if she
> went any time soon.
> Hypos are not such a problem during the day as she can deal
> with them herself but she doesn't wake with night time
> hypos. She had convulsions at night a while ago after going
> to bed with a BG of 11 and a snack containing 50g's carb.
> Luckily I was working late in the same room. I dread to
> think what would have happened if I had not been there. She
> threw up for 3 hours afterwards but didn't really wake up
> properly. I suspect that she would have had convulsions and
> vomiting without being able to come for help. I suppose it
> depends on how far away the child is from others and how
> soundly they sleep.
> We do a blood test about 2 hours after supper now and
> sometimes need to wake her for food. I haven't been able to
> spot a pattern for those nights yet.
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