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Why my child? finding it hard after 8 months
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<blockquote data-quote="helenlavery" data-source="post: 47009" data-attributes="member: 13562"><p>Hi there, my son was diagnosed with type1 July last year he is 11 years old i no exactly how u feel x i couldn't get my head round it too i was crying every day for weeks why my child but am now getting on with it as every day life because uv got to my son uses insukin pens so i cant help u with the pump dont no anything about. eye site could be coinsedince. all you can do is what im sure you are already doing being there and helping her understand things my son is going through a bad honeymoon period so we are opting for the basal/boulus to help control his bs as just now he is on the 3 daily injections but this is not get any steady bs anymore. It is an awfull lot to take in and a worry about all the complications but if u help her keep good bs then she'll be fine and adapt to every day life with the condition my son has totally amazed me he is so brave and has accepted it better that i have it is hard and confusing having to count everything they eat especially when eating out but like everything else you learn the more you do it and soon will become part of everyday routine hope u get the info your looking for just thought i'd reply as i dont no any other parents just new to the forum take care and hope to speak again soon.</p><p></p><p>Helen</p></blockquote><p></p>
[QUOTE="helenlavery, post: 47009, member: 13562"] Hi there, my son was diagnosed with type1 July last year he is 11 years old i no exactly how u feel x i couldn't get my head round it too i was crying every day for weeks why my child but am now getting on with it as every day life because uv got to my son uses insukin pens so i cant help u with the pump dont no anything about. eye site could be coinsedince. all you can do is what im sure you are already doing being there and helping her understand things my son is going through a bad honeymoon period so we are opting for the basal/boulus to help control his bs as just now he is on the 3 daily injections but this is not get any steady bs anymore. It is an awfull lot to take in and a worry about all the complications but if u help her keep good bs then she'll be fine and adapt to every day life with the condition my son has totally amazed me he is so brave and has accepted it better that i have it is hard and confusing having to count everything they eat especially when eating out but like everything else you learn the more you do it and soon will become part of everyday routine hope u get the info your looking for just thought i'd reply as i dont no any other parents just new to the forum take care and hope to speak again soon. Helen [/QUOTE]
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