The Port

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lilacbreastedroller
Posts: 90
Joined: Thu Sep 05, 2013 10:25 am

Re: The Port

Postby lilacbreastedroller » Tue Feb 17, 2015 11:44 am

It took me six months or so to really adjust to my port. I still don't like to touch the area because it feels gross, so I dont. I went to the beach last month and of course put on sunscreen. Well, I never touch the port area, so I didn't. Well.. I got a big circle of sunburn on and around my port because I never put sunscreen on it... D'oh!
dx 6/1/12@45yo
RT, 4 liv, 5 lung
7/12 FOLFOX
2/13 Xeloda 4k mg/d
7/13 DC VAX,1k mg/d metro Xel
11/13 Erbi, Irino
6/14 clinical trial lirilumab, nivolumab
9/14 Stivarga
1/15 clinical trial immunotherapy (young TILs)
RT, mets to liv, lung, adrenal, lns

Peabody5422
Posts: 334
Joined: Fri Dec 09, 2011 10:21 am
Facebook Username: debbie.whitaker

Re: The Port

Postby Peabody5422 » Tue Feb 17, 2015 5:27 pm

I had port place in my left shoulder and received a bad burn at the same time so 2 weeks later after the onoc nurses freaked out, the surgeon removed it. 5 days later I had one place in the right side with no problem. I had to go to wound care for 5 months trying to get the hole in my right side to fill in. My only issue is that my collar bones hurt right above the "old" site and above the new one. Don't know if all this chemo and surgery is the cause or I am just getting old. Ouch!
DX: RC 11/11 T1 N1c MX
Surgery: LAR 12/23/11
Rad & Xeloda: 1/12 - 4/12
Clean CT: 4/12
Reoccur: Lymp 4/14 4 new locations. 2 Aortic, 2 locations Rectum
Chemo to start: 6/14, OXI, Advastin, 5FU
10/14: One tumor left - on Avastin only
Surgeries: 4/15, 7/15 and 8/15 :last tumor w/Illeostomy then Ostomy
NED by 7/15 Surgery

Bat-Mom
Posts: 101
Joined: Sun Feb 09, 2014 8:01 pm
Location: FL was RI

Re: The Port

Postby Bat-Mom » Tue Feb 17, 2015 10:06 pm

I could see/feel the bump. It didn't bother me. Onc said I could keep or remove she didn't have a preference. I weighed superstitions. If I kept the port in it was like I was saying that I believed the cancer would come back. Then I thought if I removed it then I was tempting fate.

I ended up removing it. Hope I don't regret that.
54 y/o
10-2013 colonoscopy
11-2013 colon resect
12-2013 stage 3b results are in 4 of 11 LN
12-2013 - 5-2014 folfox
9-2014 cea 1.7 12-2014 CT clear cea 1.7 3-2015 cea 1.6
6-2015 new doc new lab. Cea now 3.9???

MrsOssie
Posts: 28
Joined: Wed Feb 06, 2013 8:04 am

Re: The Port

Postby MrsOssie » Wed Mar 04, 2015 9:35 am

I forgot about my port being in and got used to that little bump and seeing the "wire" along my collar bone.

Butt... When I was done with my chemo, I waited 6 months and then took the thing out. My onc said that, if I ever needed it reinstalled, they would have no problems putting one in again. The day the butcher/junior Dr took it out it was a great day of celebration and very gross. I took pictures of the port and then said goodbye. However, the decision to take it out was HUGE. You worry that taking it out will mean if you need chemo again then you'll have to go through the pain of having it put in again or have to get a PICC line. You also worry that taking it out means that you really don't think that you're done with chemo or cancer.

So, for me, taking it out was a symbolic F U to my 5FU and has freed up time so I don't have to have the thing flushed each month. No right or wrong way to go, IMHO.
Stage IV - 2 +ve lymph nodes & liver mets
32 F - Dxd Oct 2012
FOLFOX Dec 2012-Aug2013 (12 cycles)
Liver & colon resections, ablation, radiation & ileostomy Feb-Jun 2013
Ileostomy reversal Sept 2013
2nd Liver resection Feb 2015 - 1 met

kiwiinoz
Posts: 1170
Joined: Thu Jan 03, 2013 11:44 pm

Re: The Port

Postby kiwiinoz » Thu Mar 05, 2015 7:02 am

Had mine in for 2 years and am looking at getting it out soon.
I don't carry a lot of weight on me and it is really noticable when I wear business shirts (Mon-Fri) and when I wear short sleeved shirts (6 months of the year)
On the whole it doesn't bother me but I notice it a lot more recently when I go running and I seem to feel it perhaps as I am pushing it around a bit more.
On the whole I am really glad I have had it in but seems like a good time physically, and mentally, to have it out
Kiwi
Stage IV Rectal Cancer (39 Year old male at dx)
pT3N0M1 (wish that was M0)
Diagnosed 05 Dec 2012
LAR 05 Jan 2013
VATS 27 Feb 2013
FOLOFX April 2013 - Sep 2013
Clear Scan 03 Dec 2013 - August 2020
Port Out 26 March 2015

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elise
Posts: 1519
Joined: Fri Apr 27, 2012 5:09 pm
Location: Ontario (Canada)

Re: The Port

Postby elise » Thu Mar 05, 2015 10:59 am

I hate my port. It's uncomfortable when I lie on my side and a constant reminder of my situation. And yes I can definitely see and feel the catheter. GAG!
2012
Feb - Stage 2 (T3 N0 M0) CC @ 30
Mar - R hemicolectomy, 18 LN
May-Nov 6 - Chemo (8 Xeloda)
2013
Feb - NED
2014
Feb - NED
May - Stage 4 - 1 liver met @ 32
Jun - Liver resection
Oct - CLEAN SCAN
Aug-Jan - FOLFOX 5 rounds, 5FU X 6
2015
Ap, Oct - NED
2016
Mar - NED

Peabody5422
Posts: 334
Joined: Fri Dec 09, 2011 10:21 am
Facebook Username: debbie.whitaker

Re: The Port

Postby Peabody5422 » Thu Mar 05, 2015 11:18 am

The big yuck is that you still have to have IVs even thou you have a port. Those things hurt to someone like me with rolling veins!
DX: RC 11/11 T1 N1c MX
Surgery: LAR 12/23/11
Rad & Xeloda: 1/12 - 4/12
Clean CT: 4/12
Reoccur: Lymp 4/14 4 new locations. 2 Aortic, 2 locations Rectum
Chemo to start: 6/14, OXI, Advastin, 5FU
10/14: One tumor left - on Avastin only
Surgeries: 4/15, 7/15 and 8/15 :last tumor w/Illeostomy then Ostomy
NED by 7/15 Surgery

User avatar
mstults
Posts: 1327
Joined: Fri Nov 30, 2012 11:23 am

Re: The Port

Postby mstults » Thu Mar 05, 2015 9:27 pm

The only time I've needed IV's is for arterial gas and extra access when I was in ICU. I was sedated when in ICU so that was ok. For the artery, 3 nurses refused to touch me. The 4th got it first try. My veins are very small and hard to find. I love my port, catheter and all.
Male Age 53. Dx CC with numerous liver mets 6/23/12. Colon res 6/24/12. Started folfox 7/24/12. Added avastin 8/27/12. CT 12/27/12 still showing shrink. Took 17 rounds of FOLFOX. Then 5-FU + Avastin. Switched to Irinotecan for 1 yr. CEA rose to >400. Switched to Vectibix 2/18/15. CEA decreasing. Scans show some growth in liver mets. Lung Mets stable to shrinking.

https://www.facebook.com/michael.stults2/about?ref=home_edit_profile&section=work


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