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Cystic Fibrosis Forum (EXP)

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shaky and sweaty

ClashPunk82

New member
<blockquote>Quote<br><hr><i>Originally posted by: <b>Anonymous</b></i><br>Nicole,

I have CFRD too, do you use the pump or do you have the pen neddles? I am just using the needles but I have to take usually 5 a day for everytime I eat. I asked my doc about the pump but he says he doesn't know if it would be better for me or not. It's been 4 yrs since I've had it and it seems that I need more insulin now than i did in the beginning, do have feel the same way?



Lindsey 21, w/cf, cfrd<hr></blockquote>

Hey Lindsey. I actually use the vials. I like drawing up my insulin. The pens are ok but I prefer doing it that way! <img src="i/expressions/face-icon-small-happy.gif" border="0"> I never really wanted to do the pump because it just isn't my thing. I have had diabetes for 7 years now and have been on insulin for maybe 4 or 5. I do need more than I did when I first started and I use different insulin than I did back then. I take humalogue and lantus and then I take NPH at bedtime for my tube feedings. It's a lot to take during the day but I am so used to it now I don't think about it much. I hope you are doing well!! <img src="i/expressions/face-icon-small-tongue.gif" border="0">
 
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