beautifulsoul
Super Moderator
I have a question for those of you with CFRD... I only used insulin before my tube feeds at night but since the lung transplant my blood sugars have been really high through out the day too. I went for an appointment today and the doctor said I now need insulin before I eat meals. They showed me an insulin pump, saying I won't need a shot everytime I eat something. I don't really like the idea of it. My question is does anyone else have an insulin pump? What did you think of it before you got it and do you like it now? Do you have to take it out and back in to shower? Any input would be great thanks!