didie said:For me diabetes has been a very positive experience because I'm now fitter than I have been for over 30 years.
However I do hate it when doctors/diabetic nurse ask me about my mood. I understand that some people get depressed with diabetes which must be a horrible experience for them, but I hate the assumption that we're all going to be that way. That's what put me off going on the DESMOND course - the questionnaire about my feelings. I had it doubly at the start because of my stroke - was I depressed about that? Nope, I wasn't depressed, but very grateful to be alive and have a second chance, to have a condition that I could control myself and I just got on with it.
This post has tugged at my heart strings ,SophiaW said:As a parent of a child with diabetes the hardest part for me has to be the fact that you never get a break from it, it's relentless, it never sleeps, has a weekend off or goes away on holiday. Whatever you do and wherever you go it's there constantly demanding attention - either dosing insulin, checking bg, set changes or calculating food, snacks and exercise. When your child becomes ill it steps up a gear and becomes like a demanding nagging pain in the rear end threatening a rise in ketones and a hospital admission if you get it wrong. I would love to be able to give my daughter (and myself) an occasional break from diabetes so that she can go for a sleep-over, have a holiday or a fun day out without fussing over the management of it all.
I asked my daughter what she finds the hardest part. Her answer: having to be sensible about what she eats when all her friends are eating what they want and she knows that she can't do the same. She is referring to functions like parties and school fetes where the other kids might be having cakes, sweets, ice cream etc. She is allowed one treat but can't have all of those things together like some of the other kids will do.
anna29 said:This post has tugged at my heart strings ,SophiaW said:As a parent of a child with diabetes the hardest part for me has to be the fact that you never get a break from it, it's relentless, it never sleeps, has a weekend off or goes away on holiday. Whatever you do and wherever you go it's there constantly demanding attention - either dosing insulin, checking bg, set changes or calculating food, snacks and exercise. When your child becomes ill it steps up a gear and becomes like a demanding nagging pain in the rear end threatening a rise in ketones and a hospital admission if you get it wrong. I would love to be able to give my daughter (and myself) an occasional break from diabetes so that she can go for a sleep-over, have a holiday or a fun day out without fussing over the management of it all.
I asked my daughter what she finds the hardest part. Her answer: having to be sensible about what she eats when all her friends are eating what they want and she knows that she can't do the same. She is referring to functions like parties and school fetes where the other kids might be having cakes, sweets, ice cream etc. She is allowed one treat but can't have all of those things together like some of the other kids will do.
it cant be easy for the youngsters and their parents,
As they walk every step of this journey with their child...
So true sophia it is a condition that never sleeps nor gives us a day off !
Much love and thoughts to both of you.
Anna.
didie said:However I do hate it when doctors/diabetic nurse ask me about my mood. I understand that some people get depressed with diabetes which must be a horrible experience for them, but I hate the assumption that we're all going to be that way. That's what put me off going on the DESMOND course - the questionnaire about my feelings. I had it doubly at the start because of my stroke - was I depressed about that? Nope, I wasn't depressed, but very grateful to be alive and have a second chance
anna29 said:Hi all.
With these replies and input from the childrens parents.
I have often wondered do the children cope/adapt to it 'better' than us adults ?
Meaning do the children accept it as a life experience not knowing the difference
away from it due to being such younger ages when diagnosed.
Not knowing or having memories of life pre diagnosis.
Have wondered if I would have tollerated/adapted to it better if was far younger?
The childrens parents deserve a medal to cope with this lifestyle to implement and lead and tollerate.
Not to mention the sheer worry/stress it must bring at times for their so loved children.
Anna.
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