Hi my 2 year old daughter also diagnosed at Christmas so I feel what you are going through. It does get easier for them with time. I can say that I have been at the lowest point ever after her diagnosis as I struggle badly with the anxiety of what's going on, is she hyper or hypo! I Am coming to terms with things but it all takes time. My daughter is now coping a lot better with it than I am. Carb free snacks are nuts, meat, cheeses. Low carbs hummous, few blueberries,( handful is about 6g ) blackberries are also low in carbs. Carbs and cals app for phone or book I have found very useful for carb counting. My daughter ate me out of house and home when she got home after diagnosis so to have a pile of carb free snacks around helped us out to. Hope you are ok, be strong from one mummy to another. XThanks everyone for the advice, can anyone also advise me on carb free snacks for a child , because he hates salad or give me a link, would be a lot of help.
The overall carb content per 100g of 70/80% dark chocolate is usually lower than milk chocolate.Out of interest Would you find that milk chocolate will cause you to spike @urbanracer? Or do you just mean the sugar contents is higher in milk chocolate?
Ok thank youThe overall carb content per 100g of 70/80% dark chocolate is usually lower than milk chocolate.
Hi, I have just found this site, my 10 year old son was diagnosed type 1 just 6 weeks ago, sometimes the injections are very painful and it breaks my heart to see him trying to be brave, I do some of the injections and it is horrible to hurt him. He gets very fed up sometimes but things are getting a bit better and on a good day I can see the boy he was before being diagnosed.We have been discussing using a pump and he is going to try one out in the easter holidays, the one with the bluetooth and no tubes, I will post how he gets on with it. Our nurse is very positive about it and there is a 4 year old girl and a 5 year old boy in our area that use pumps, good luck and try to be strong. I will answer anything you ask but it is a very confusing condition wish it was just 4 injections a day without worrying about diet, exercise hypos and all the rest.hi, this is my first post
So basically 2 months ago my four year old son was diagnosed with type 1 diabetes , and it's so hard to come to term with for me more than him. As a mother I feel devestated that I have to inject him as he hates needles and I hate hurting him , he's used to more now but he's always asking why it's happened to him suddenly.
I want him to have the best treatment so this situation isn't as bad, like what's the best blood glucose monitor as it the least painful , and what's better injections or pump, I mentioned the pump to his nurse and she didn't seem keen , I feel as they just want me to get along with the routine I've made but I don't want my son to endure 4 injections daily for the rest of his life, which scares me.
Is there anybody that has a child and how are they coping and what's best pump or injections
I understand that high BGs can make one a bit tetchy, and prior to D-day I experienced this myself without understanding what was going on. I 'feel' almost serene now that I'm down to reasonable levels. A persons emotions can be directly affected by BG control, I'm not saying categorically that it's the reason for any mood swings but it may be worth bearing in mind. You could probably see if there is any correlation without too much difficulty.And elod I can totally relate about the up and down days , his behaviour has become a lot moody since he's beeen diagnosed but there are some good days when he reminds me of how he used to be.
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