Ports.
Everything you need to know about ……….. Ports. From the patient’s perspective. If you keep reading here, you’re going to be subjected to my own unique brand of gallows humor. Just a warning.
So you have cancer and your doc starts talking about this thing called a port. No, unfortunately I’m not talking about ship ports. I’m talking about a mediport for chemotherapy.
People keep asking me questions about my port — mainly people starting or going through chemotherapy. People seem to be more curious about the port than anything else (I even find lots of people searching about them arrive here through random searches of Google or Yahoo). So … in the interest of hopefully cutting down on how many emails I get about ports … Here’s what I can tell you. As always, your mileage may vary.
What is a port?
A port is short for “mediport.” A port is a small device that is implanted under your skin so that medicine may be delivered directly into your blood system. Blood can also be drawn out of the port to be sampled. The port is sometimes also called a venous access catheter.
Why would I want or need a port?
There are a few reasons you might want or need a port.
1) Certain chemotherapy drugs (including those used to treat Hodgkin’s Disease) can cause serious irritation to the veins when they are infused. When the drug is injected through the port rather than into another vein (such as one in your arm), the drug doesn’t directly enter the skin and the likelihood to cause irritation is drastically reduced.
2) Frequent use of the peripheral veins (i.e. those in your arms and hands) can cause scarring and make the veins difficult or impossible to access. The port “saves” a lot of wear and tear on these veins. Most blood draws and treatments can be given through the port.
3) If you are getting frequent treatment or need frequent blood draws, a port (as opposed to another device) allows you to swim, shower, and basically maintain regular activities.
How does it work?
The port is placed completely under the skin, usually on the chest below the collarbones, but other locations can be used as well if desired or necessary. The port forms a small bump under the skin. This raised part is called the port’s reservoir. The reservoir has a plastic membrane or bubble of self-sealing rubber in it called a septum. The septum leads directly into a large vein or artery.
A nurse uses a special needle called a Huber (or “butterfly”) needle to “access” the port. The nurse places the Huber needle through the reservoir and into the septum. This allows access to the large vein. The nurse can then either draw blood, inject medication, or simply leave the needle in place for future use.
What does it look like?
I took some pictures of my port to show people what it looks like. I’ve found most people are really curious and have never seen a port before. I had no clue what one looked like and had trouble finding any pictures — so hopefully this helps “explain” what a port looks like and gives you more of an idea of what to expect. (If you’re like me, you like to know EXACTLY what you’re in for.)
First, this is what a port looks like when it’s actually hooked up and accessed. The dressing is placed over the top of it to keep it clean and dry. The clear tube coming out of the port is what gets hooked up to the IV machine or to the syringe for chemo. I took this picture on one of the few days I actually had my port left accessed at home.
This is what the port looks like all hooked up for chemo or any other infusion. A port can be used not only to deliver chemo, but for routine blood draws and even to just give you nice drugs like fluids. When it is not hooked up, it looks like a little bump underneath the skin about the size of a nickel with a scar above it. That’s it. (When the port is accessed, you can’t get it wet. But sometimes I would have to see my oncologist the day before chemo and he’d draw labs … to avoid the second stick the next morning when I got chemo, I’d sometimes leave the port accessed over night.)
What does a port itself actually look like?

A port looks something like the image to the left. This is the reservoir part. Ports come in different sizes. The standard adult size port is about the size of a quarter. I have a pediatric port because my mediastinal lymphadenopathy was so large that a standard size port wouldn’t fit. My port is about the size of a dime.
There is a catheter (the long tube like extension attached to the reservoir) attached to the port that leads from the port itself into a large vein or artery.
How long can you keep a port?
A port can be kept indefinitely. Reasons to remove a port include problems with it (such as infection) or simply because it isn’t needed anymore.
When not used regularly, a port needs to be occasionally flushed with heparin to keep it functioning properly.
How did they put it in?
My port was placed using just local anesthetic. It was done in a surgery room in the radiology department. The surgeon made two incisions — one on the right side of my chest below the collar bone and a second incision in my neck on the same side. The chest incision was the “pocket” where the port itself was placed. The second smaller incision was for tunneling the catheter.
I think the standard procedure is to actually put the port on the left. Mine went on the right side because I had so many masses in my chest.
Did it hurt to put it in?
Not really. It was more unpleasant than painful. I had the option for more anesthesia than just local, but to be honest for me the risk of anesthesia would outweigh the mild unpleasantness factor.
The painful part was injecting the lidocaine. That felt like getting stung over and over by a bee. Pleasant? No. Painful? A little, but totally doable.
When the surgeon was actually working on the port, it felt like he was tugging at me. Not painful, just strange.
Does accessing the port hurt?
Accessing the port still requires a needle stick. It hurts probably just as much as getting an IV in the arm, but the advantage of the port for me is there was only one time that required two sticks. I have lost count of how many times I’ve needed to be stuck more than once for an IV or blood draw.
What does the scar look like?
See above. Although there was also an incision on my neck, I don’t seem to have any scar there. That incision was quite small.
Does having a port effect your daily life?
I run with my port, I shower … I usually forget it’s there except for when a seat belt occasionally rubs up against it or something. I like the port because my veins aren’t very good and the port saves a lot of needle sticks.
Anyway, I hope this helps demystify the port!

on February 1, 2008 on 4:03 pm
Thank you for having the courage to show what a port looks like. I was just diagnosed with cancer (not Hodgkin’s) and my doctor wants me to get a port. Seeing what it actually looks like makes it A LOT less scary. So thank you for posting this.
on February 1, 2008 on 6:43 pm
thanks for the post. Oh how I hated my port. I loved so much about it but I also hated it. The scar is interesting and is sort of like a handshake into a secret club. At time people will point to my port scar and then pull down the neck of their shirt to show me their scar. In those moments I feel equally honored and exposed. Again, good on you for posting about it.
Jenne
on February 1, 2008 on 7:30 pm
Your one tuff young lady just reading about your
port makes my skin crawl.
on February 2, 2008 on 1:49 pm
Thanks for the port porn! (Sorry, couldn’t resist the alliteration).
on February 2, 2008 on 2:23 pm
Jenny, Thanks for your post on the port. My husband, Kevin (Civil War Memory) pointed out your great blog to me. While I am not a historian, I love reading about history by “association”. But in this case your post on the port was interesting for me because my sister just finished chemo and radiation last year. She is doing very well. However, I wished she would have been offered a port because the chemo destroyed her veins. More important so, you sound like a fighter and your attitude reminds me of my sister’s. Keep it up.
on February 2, 2008 on 3:46 pm
Anybody who can post this REALLY has their head on straight….no wonder that you bounce back from the rough spots….
on February 4, 2008 on 12:32 pm
Amanda, best of luck with your treatment.
Jenne, I love your blog. Good to see another Hodge survivor with a well-developed sense of humor.
Randy, thanks … The port actually wasn’t that bad. And getting it wasn’t very painful even though I just chose the local anesthetic route.
Ben, I knew you’d LOVE the port porn.
Michaela, thanks for checking out my blog. My oncologist considered ports mandatory, and since I had eight months worth of chemo, I’m glad he did. I hope your sister continues to do GREAT!
Bob, I dunno how straight.
on March 26, 2008 on 5:05 pm
Do you know that many dogs, cats and even ferrets also have ports for chemotherapy – and they seem to love them – the owners say it is better than their pets being poked and prodded to find a vein.
on April 20, 2008 on 8:25 pm
Thank you for sharing your information. I was diagnosed 1 month ago uT3 N2…and have to have chemo/rad prior to surgery and chemo post-surgery. Your facts and humor helped me more than you will ever know. Thank you..and God Bless.
on April 27, 2008 on 8:08 pm
thank you for all the Hodgkins/port info. My sister-in-law was recently diagnosed with Stage IIB
Hodgkins. I am one of her primary care givers and she has really “handed over” to us all the decisions, information etc. about her disease…we decipher all the technical aspects, side effects, possible protocols etc. and then in turn simplify her treatment options and disease info for her. You have aided me greatly and I will educate her on what to expect and your experiences.
on September 15, 2008 on 3:39 pm
Thanks for this info – I was just diagnosed with Hodgkin’s 2 weeks ago, Stage 2a. I’m a 28 year old female just like you – and it came out of nowhere. I start chemo next week and will decide after this first one whether I should get a port or not.
Maybe I will now that I have read your blog. Im am not into needles, I mean I profusely sweat when I even think about one. So, this has not been easy for me.
Thanks for all of the info – I am still in shock!
I hope you are doing well and hopefully you are done with Chemo by now! Wish me luck…
on November 1, 2008 on 12:18 am
[...] Ports [...]
on December 29, 2008 on 2:34 pm
Hey there, its Kerri again. I am having my 8th treatment tomorrow, and yes I did decide to get a port. It has been a life saver! Anyone who is thinking about getting one definitely should, it just makes your life so much easier and less painful. My oncologist has decided I should have 9 total treatments, odd number I know. So I will have 4.5 rounds. I guess he just wants to be sure. I will start radiation in February. I did not lose all of my hair, but its pretty thin right now and very frail. It sticks up everywhere because it has broken off in so many places. I try to be so careful with it, but its hard. Im sick of the hair all over my house, it’s pretty gross and frustrating at times. But, its better than losing all of it I guess. Every time I touch it some falls out. Anyways, I just wanted to write again and give an update since the previous post was before I even started treatment. For all of you newbies out there, don’t worry – everything is going to be ok. It’s tough – but its definitely something you can handle. Be strong and this too shall pass. Best of luck to all of the newly diagnosed Hodgie’s on here!
on December 30, 2008 on 10:31 pm
Hi Kerri,
I’m a 30 year old who was recently diagnosed with Hodgkins’s lymphoma. I had my port placement today. I am scheduled to begin my first round of chemo next week. I am a bit nevous because I really don’t know what to expect. How did you feel after your first round of chemo?
on March 4, 2009 on 2:36 am
Thanks you so much for this very valuable information on mediports. My little twin girls Addi and Cassi have Niemann Pick Type C disease which is often referred to as the “childhood Alzheimer’s.”
They will be the first in the US to get infusions of a sugar compound called cyclodextrin and it’s going to be administered through a mediport just like they do for cancer patients. I have been very scared about putting the ports into them and sticking them all the time for the infusions and I can’t thank you enough for demystifying the entire process.
Do you ever get the numbing cream put on your skin so you can’t feel the prick? I think this might help and I plan to do this with my girls so the don’t feel the prick.
I am going to do a blog on this topic and I will point to your informative website for information!
Thanks Again,
Chris Hempel
on April 15, 2009 on 1:49 pm
Thanks for sharing you really helped me understand all that is involved in using and having a port installed.
Anne
on May 17, 2009 on 10:35 pm
[...] morning at 8am Bex will have a port installed through which all of her chemotherapy is administered. The eventual stem cell transplant also [...]
on May 22, 2009 on 12:11 am
hi, great info, just one further question. my husband was just diagnosed with hodgkins and was wondering if he can still lift weights with the port? I heard it can shift the position of the port/ dislodge slightly? what do you think? how are you doing now? we are just beginning this bullshit and are very anxious….. best of luck hope you are doing well…..