
ports
Warning, am bored, am still a little sick, have digital camera, need to entertain self.
This post is solely Hodgkin’s Disease / cancer related; if you want to skip down to the Civil War stuff, go to the Civil War posts and enjoy the second post about ……. the history of Hodgkin’s Disease. haha. Actually Hodgkin was alive during the Civil War, there’s a tenuous connection. Ok. If you’re still here, you’re reading a post about cancer ……
Since I’m bored, I decided to write about my port.
No, unfortunately I’m not talking about Admiralty law. The law of the high seas. You know. Arrrrgggggghhhhhh. Pirates! Didn’t you read the whole “I’m talking about cancer” disclaimer above? Don’t you know I make it a practice not to talk about the practice of law even though I’m a lawyer? I’m talking about a mediport for chemotherapy. (Sorry about so many cancer-related posts this week. These things run in streaks, you know?)
People keep asking me about my port — mainly people starting or going through chemotherapy, 1 but also people who are just curious. 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 (ok, I’m kidding, I love hearing from readers even if it is about ports) AND BECAUSE I LIKE HELPING PEOPLE :) … Here’s what I can tell you. As always, your mileage may vary.
All right, for the morbidly curious or for those who really want to know because they are considering getting one … I got tired of the questions, mustered up my courage, and took a picture of Victor. By the way, I did name my port. Victor. As in I love the smell of napalm in the morning … Smells like … VICTORY. (Or the death of thousands of Reed-Sternberg cells. Same difference.)
(Any doubt that this is my port can be dispelled by noting the copy of “Gray Fox” among other Civil War titles in the background on the shelves.)
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.
(Generally, your port is only hooked up like this for an infusion or for a test. I had to have a PET scan following some blood work, and to avoid two needle sticks, I told them to leave the port in — which is why I have it accessed at home.)
Here is a close up of my chest port scar. It’s located about an inch below my collarbone on the left side of my chest (usually ports go on the right; I had too much supraclavicular and chest lymphadenopathy going on in the right side).
OK, now let me let you in on some secrets about the port. The stuff your doctors may or may not tell you but I think are important from a patient’s perspective.
(You may not want to continue if you don’t like gallows humor. I like gallows humor very much. And if I’m not employing it, chances are I’m REALLY sick, so take it as a good sign, not a bad.)
1. Get a power port!
Not just because it sounds so much cooler when you strut around chemo, pulling your IV pole behind you …. “My port’s a POWER PORT.” Actually you want a power port if possible because they are really much more useful. This is the type of power port the Cleveland Clinic gave me.
A power port comes in handy because it can be used for CT scans. CT scans use a special pump to inject the dye that can destroy or damage a regular port. A power port is specially designed to be used for CT scans.
2. They make two incisions.
Getting a port is usually an out-patient surgery. A general surgeon or a vascular surgeon can put it in (mine was done by a vascular surgeon). They will give you drugs to go to sleep or you can go hardcore with just local anesthesia and bug the surgeon like I did. (My surgeon was so cool.) The surgery took about half an hour.
The surgeon makes an incision to put the port in on your chest, then he makes a smaller incision near the neck to tunnel the catheter. (The tunneling felt FREAKY) I have a scar on my chest but no scar in my neck, though if you look very carefully and know what to look for, you can see the line running up in my neck vein.
Pain wise … I was awake. The liodocaine (the local anesthetic) burns and stings. Other than that, you mainly feel like someone is tugging and pulling at you. Scale of 1-10 with 10 being please kill me now, the port surgery was about a 2-3.
Visibly, unless you’re showing off your chest, no one should know you have a port unless they know something about them and then who cares? My scar is hidden when I wear a sports bra, so even then you can’t see it. Good job, Doc. :)
3. Needles?
Yeah. There are still needles. They use a special type of needle to access a port. 2 You do get stabbed, except there is no need to hunt for a vein and rather than getting stuck in your arm, you get stuck in your chest. By the way, stabbing a port is called “accessing it.” Nice euphemism, but it just means stabbing.
Your chest has less nerve endings, so the stabbing isn’t close to as bad, especially since they almost never ever miss. Plus you can put cream on it to numb it before you go get stabbed if you really are afraid of needles (I never used the cream so I dunno how well it works). Also, there is no cumulative damage to your arm, hand, or other veins.
4. Don’t expect everyone to know what to do with a port.
Unfortunately while any good cancer or chemotherapy center will know what to do with a port, don’t be surprised if nurses or techs in other areas don’t know how to access it. Don’t be surprised if you even hear “what’s a port” and be sure to warn the x-ray people that it’s there so they don’t flip out about the weird thing in your chest.
Also, it’s a good idea to carry your port card (basically just a card that says you have a mediport) because it can set off medal detectors, though usually only REALLY sensitive ones (I’ve had no problem at the airport with mine).
5. But using it at least for chemo will save your veins …
Certain chemo drugs, including many used to treat Hodgkin’s, can literally burn you inside out. And if the IV leaks, you’ll end up with a painful problem. The port saves you a lot of that problem with ruining your veins, plus if your doctor is like mine, he will love to get your blood as often as possible. (Hematologist is medical speak for vampire. I’m positive.)
6. I forget it’s there. But you do gotta keep it flushed.
Seriously, I am a little leery about touching the spot, but most of the time I don’t even think about my port. You can’t really feel it or anything like that.
When you’re out of treatment, you have to get your port accessed and flushed every six weeks. It takes like five minutes, but it something to consider in keeping your port long-term. I’m kind of attached to mine (cue laugh track), but Dr. S is too conservative to let me take it out short of 2 years anyway.
Doctors seem to have different “rules” on when you can have your port removed. My doctor insists on remission for two years. Your mileage may vary.
7. Badge of Honor
When I see someone with a port scar (sometimes they are higher on the chest than mine for example or the scar is bigger for some reason) or pick up on the neck catheter, I think ah there goes another chemo warrior, a survivor like me. Seriously.
8. Sometimes your doc will attack your arms anyway.
Sometimes for various reasons, you doctor will have to get blood drawn peripherally anyway. (For example, if there’s something wrong with the port or he suspects an infection in it … or for certain tests, or because you said something mean and he’s mad at you and trying to make you life miserable … you do know I’m kidding about that last one right?).
9. It doesn’t save you from shots.
Yup, Neulasta (white cell booster) and Arnasep (red cell booster) seem to be given as shots, so you’re still getting stabbed for those. The port just reduces the stabbings somewhat. Basically anything you can use an IV for, the port can be used for.
10. Having a port can be fun.
A confession. One time I was goofing around with one of my local running friends and we told the rest of a group (who didn’t know I had cancer) that I had been abducted by aliens. When they guffawed, I showed them the scar and said that was the tracking device. You should have watched their jaws drop. (OK, so you guys all know I have a good sense of gallows humor! This proves it!)
- I wish no one ever had to go through chemotherapy again ever. [↩]
- It’s called a Huber Needle, if you really want to know. [↩]
Tags: ABVD, cancer, chemotherapy, hematology, Hodgkin's Disease, oncology, ports

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.
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
Your one tuff young lady just reading about your
port makes my skin crawl.
Thanks for the port porn! (Sorry, couldn’t resist the alliteration).
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.
Anybody who can post this REALLY has their head on straight….no wonder that you bounce back from the rough spots….
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. :)
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.
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.
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.