I've been on the pump for 7 years now. I love it. I can't swim with mine though. Do I need to ask for an updated version. Mine is not waterproof.
I can detatch it for up to two hrs but I don't .
The insulin is despensed by a cathetar attatched to the pump itself. There is no needle after the initial prick of the site change. The catheter is about the size of a folicle of hair which stays in you and is very flexible. Im a little sensitive to it sometimes cause I am too thin right now. I use the pen to put in a subcutaneous site. But once I gain a little weight that sensitivity to the cathetar goes away. I find that it has helped me feel better, gain a bit of weight when Im well. Interestingly enough the BS monitoring that goes along with the pump lets me know when I'm getting sick about 5 weeks before I get an exacerbation and have to go in to the hospital My blood sugars reflect the infection coming on. Amazing.
I love my pump.
Being so thin I find it a challenge to find plenty of spots to inject the catheter but It works out.
Well thanks for letting me blabber. I have never had another CF person to share pump journeys with. This is so cool.
<img src="i/expressions/face-icon-small-happy.gif" border="0">
JenWren
I can detatch it for up to two hrs but I don't .
The insulin is despensed by a cathetar attatched to the pump itself. There is no needle after the initial prick of the site change. The catheter is about the size of a folicle of hair which stays in you and is very flexible. Im a little sensitive to it sometimes cause I am too thin right now. I use the pen to put in a subcutaneous site. But once I gain a little weight that sensitivity to the cathetar goes away. I find that it has helped me feel better, gain a bit of weight when Im well. Interestingly enough the BS monitoring that goes along with the pump lets me know when I'm getting sick about 5 weeks before I get an exacerbation and have to go in to the hospital My blood sugars reflect the infection coming on. Amazing.
I love my pump.
Being so thin I find it a challenge to find plenty of spots to inject the catheter but It works out.
Well thanks for letting me blabber. I have never had another CF person to share pump journeys with. This is so cool.
<img src="i/expressions/face-icon-small-happy.gif" border="0">
JenWren