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20,000 children with diabetes not getting the care they need to achieve good control

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That's terrible. As adults we struggle and complain about lack of support. For my part, although I want to stay healthy and try to do the right things, I have seen something of life. Children have seen hardly anything so need that extra support and care, they are our future.

I think also the parents need the support too. The parents here are well informed and proactive in the care of their children, but not everyone has access to resources like this one.
 
That is out of order!

Although I do wonder if perhaps with children maybe they are setting things slightly higher due to dangerous hypos? I know of someone that has higher HbA1C recomedation because of that. Plus hormones especially since they have stated most being around teenager age, it is probably worth keeping children up to the age of 18 (maybe even 20) in pediatric care, I never was in it, since they are still growing right up until then and if the child has had the same care since a very young age their Endo would know them best and how things work for them!

Also I can certainly say that throughout being diagnosed with diabetes from the age of 16 I've never had decent care - and I know they don't really know whats going on but they should tell us their side of the story. Even my own mother didn't understand Type 1 Diabetes... because they never told us. So it seems that not only is the care itself bad the knowledge and support given is equally terrible. I haven't seen a DSN in probably two years now O_o.

I think as you can see, I have been affected by lack of care AND it makes me angry!!! Just glad i found this place 🙂
 
Wow. That is really shocking. :(
 
It seems to me that, once again, education is everything. Not just for the kids, but for their parents and medical staff as well. It's all very well giving them their meds and hopefully, regular testing, but everyone involved in the child's life needs to understand what the condition is and what it can do if no-one is taught how to manage it. None of us can be in absolute control of our diabetes, the condition itself won't premit that, but we can try. We can only do so though, if we have the right tools and the right support.

Sadly, it seems to me that folk with chronic conditions that need long term management are not a focus of our health system. It's not just diabetics who regularly slip through the cracks but others too, such as asthmatics. Unless you make a pest of yourself medical folk are going to assume everything's fine.

I was lucky, at diagnosis the doctor I had then sat me down and told me what was wrong, what to do about it and how to do it. He also gave me all I needed to make a start with testing kit, strips (both BG and Ketone), diet sheets and exercise sheets. He and the DSN there weee very supportive, but that I've since discovered is comparatively rare and since my return home, I've had fight to get the care and support I believe I need to handle this thrice dammt Big D. Of course, the Big D itself has thrown me plenty of curve balls so that I don't know what I'd have done if I hadn't managed to beat Dr Idiot into submission and get referred to the clinic.

It's going to give me nightmares knowing that there are youngsters out there without any proprer support.
 
That is worrying stats. When I was diagnosed at 16 my experience of my support was poor so I am not shocked by this just appalled that things haven't improved. It would have helped if I was kept on the childrens ward not put in an outpatients ward with lots of older patients where the staff forgot to give me my insulin and tried to feed me frosties for breakfast! I didn't get any emotional support either, I think this is essential for children as it is for all of us really.
 
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This thread is now closed. Please contact Anna DUK, Ieva DUK or everydayupsanddowns if you would like it re-opened.
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