CSN Login
Members Online: 20

Power Port

Landranger25's picture
Landranger25
Posts: 207
Joined: Nov 2009

Had to go today and get my port flushed. Go every 4-6 weeks as I'm sure do the rest of you. I am 5 months post chemo and was wondering what you were told as to how long you might have the port. In the beginning my Doc said about a year which for me will be the month of July. Is there anyone into the second year? Just curious. Thanks in advance.

Mike

Fire34
Posts: 351
Joined: Feb 2010

Mike
I sure wish I had a power port for mine. Due to my course of treatment I had a dual port a cath. I wish mine lasted 5 monts post treatment. Mine lasted about 2. It got infected and had to be removed. About the fourth week of treatment mine started to block off and they blasted it with blood thinners and kept it going. My veins are coming back and I go quarterly now so I am not to worried.
Dave

Kent Cass's picture
Kent Cass
Posts: 1746
Joined: Nov 2009

I was told at the start by my ENT that I'd likely have the Port for 3 years. Go in at the start of every month to get flushed with Hebrin (sp), and something else. "Take a deep breath," kinda time. In a way, my fellow Survivors, with my now being almost-17-months, it is a reminder kinda time for me. Always get it done at High Noon, so I gotta punch-out at work, along with changing my clothes. Thing is, it's a reminder to everyone at work, also. Lest anyone forget, you know, that I've done battle with the monster C, and have so-far won that very large battle...

kcass

CajunEagle's picture
CajunEagle
Posts: 357
Joined: Oct 2009

That's strange. None of the Doctors have ever told me to have my medi-port checked out to see if it still works correctly. Guess this is ANOTHER ONE of these dang procedures that I'm suppose to initiate. Kind of like the Pet-Scan I'm getting tommorrow....I've I hadn't asked about it last week, they would have forgotten all about it. I take Jantoven (a blood thinner) every night due to the medi-port. Suppose I'd better find out.

Larry

Hondo's picture
Hondo
Posts: 5717
Joined: Apr 2009

All the best to you on your PET tomorrow

CajunEagle's picture
CajunEagle
Posts: 357
Joined: Oct 2009

Let's go do it and have NO SURPRISES.

pattyanny's picture
pattyanny
Posts: 523
Joined: Jul 2009

Good luck with your PET tomorrow. Know my prayers are with you! Get that port flushed!

Skiffin16's picture
Skiffin16
Posts: 8062
Joined: Sep 2009

Sounds like another of those features where opinions vary a little.

My chemo doctor has me come in every 6 - 8 weeks to have the port flushed. As for removal she feels that two years is the time frame. We went over this on my last visit a few weeks ago, after having blood work and my routine three month CT.

My blood work has finally come back in to all normal ranges (first time since my initial diagnosis January 2009). The CT was good with no changes also.

She moved me to a six month schedule on scans, next being the PET in August. If everything stays good she said she'll schedule me for the port to be removed February 2011 (two years from the implant).

John

ratface's picture
ratface
Posts: 1235
Joined: Aug 2009

My ENT said she would just remove it while doing the neck disection. That was right after chemo and radiation. I never questioned it. I suppose they can put the damn thing back in if needed.

Subscribe with RSS
About Cancer Society

The content on this site is for informational purposes only. It is not a substitute for professional medical advice. Do not use this information to diagnose or treat a health problem or disease without consulting with a qualified healthcare provider. Please consult your healthcare provider with any questions or concerns you may have regarding your condition. Use of this online service is subject to the disclaimer and the terms and conditions.

Copyright 2000-2014 © Cancer Survivors Network