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Phoenix, your answer was so relevant to me, it answered a question I have been asking myself since being diagnosed. I was almost there, but couldn't quite get my head around the fact that I needed glucose throughout my exercise, as everyone else seems to say reducing your bolus before exercise...

I reuse my needles too, but only when I use Novorapid. I tend to use the same one all day and then dispose of it. I don't reuse needles when using Levemir as I found it seemed to clog up the pen. I haven't really had any problems yet except for injections being more painful and suffering more...

Louise, the foot pain could possibly be cramp. I had the most awful cramp in my feet, particularly at night, before being diagnosed. Hope everything goes okay at the doctors.

I had to reorder my meter, but it was sent out within 2 days, so excellent service. I love the finger pricker, it doesn't hurt half as much as my freestyle freedom lite. I'm not used to using a new lancet every time I test, in fact I probably only change to a new lancet once every 3 weeks...

sugar2 Do you mean the cartridges that go inside the novopen, if so, then yes I use Levemir cartridges, and so does my son.

DAFNE isn't available in Portsmouth, although the diabetic clinic do run education courses. Anything that helps to easily track blood glucose is welcome.

Squirrel, yes I did register from the same address and same computer. So maybe that's why!

My son's meter arrived this morning, but mine didn't!

I also use Novopens, with insulin cartridges. I didn't realise there were such things as disposable pens, why would they be necessary?

It seems that no matter how you bring up your child, whether breastfed or not, there is always something that you will be blamed for. I have breastfed all my children, far beyond the recommended 6 months, yet the eldest 3 all have hayfever, the second youngest has asthma, and my youngest has...

Excellent, thanks Stu.

Some diabetic children do seem to take longer to recover from viruses than others. My son was ill before Christmas, he had two weeks off school. I don't understand about the leg pain, do you mean in the joints? My son complains about pain in his legs a lot, but having been checked out by the...

I think inheritance does play a part in type 1. I'm type 1, my youngest son is also type one, and my sister's son is type 1.

Sounds like constructive dismissal to me Jimbo, I think you should pursue this further.

Hi Helen I have a son aged 13, diagnosed in June last year. I'm also type 1. You should be able to find someone to answer whatever questions you may have here.

I've been told that I 'don't look like a diabetic', more than once, lol. What does a diabetic look like then I wonder.

I had a c-peptide test and then afterwards a GAD test, which confirmed I was a type 1. Luckily because there is type 1 in my family already, the doctor didn't waste time putting me on tablets, instead I went straight onto insulin, but she still wanted to make sure there hadn't been a mistake in...

My last hbA1c was 7.5, taken in October, but that was when I was on Mixtard, with blood glucose all over the place. I've changed now to a basal/bolus regime and would expect (hope) my next test will be lower.

Ah yes, the sweats! I'd forgotten about sweating, even though it's probably the first symptom I have of night hypos. I do find that when I go very low I can feel really awful, I hate hypos! I haven't tried glucose tablets, although my son loves them, we do tend to stick to jelly beans. Glucogel...

I don't like potatoes, or bread, but must admit I still eat them. My downfall is porridge, I love it. I'm not sure how I would manage my bolus injections if I wasn't eating carbs, I have a feeling that I would always be having hypos.