First port access tomorrow

Crohn's Disease Forum

Help Support Crohn's Disease Forum:

Joined
Jan 7, 2014
Messages
130
It's been 4 weeks since my power port was placed -- it's still sore, but I'm assuming that's normal since it's a foreign device in there?! Anyway tomorrow is my port access prior to an MRI - as per your suggestions, I did pick up emla cream so I'm assuming that it'll be relatively painless, but I'm nervous about the flush and then the contrast - you know, like just making sure it works! I wish it was my infusion team needling in the first time but such is life... How will they know if it's... Working?
 
They draw blood from it to see if it's working. For myself I knew it was working when they pushed in saline and heparin as you could feel the saline and the heparin made me light headed. Although I'm sure your appointment is done by now. How did it go? :)
 
Thanks Jennifer! It went fine - i shouldn't have been so nervous!! I don't know if they drew blood or not because they told me to turn me head for infection purposes. I actually couldn't feel the saline or heparin at all which I thought was weird lol! I have remicade on March 4 which will be my first one since the port! I can always feel that!! So I'll be interested to see if it feels different thru the port!
 
Back
Top