Tag: Portacath

What’s Done is DONE!!

These days I’m thinking about being DONE and what it means for me to be DONE (yell a bit when I put done in caps, ok?). 

I’ll break it down a bit for you. In the next two weeks I have:

  1. a meeting with my surgeon
  2. my final Herceptin treatment
  3. my portacath removed

Each of these appointments represent a different kind of DONE (nice job) and a bit WOOT WOOT (emphasis here too, please, maybe twist your wrists in a circle).

Surgeon Visit

First of all, surgeon man is very charming WOOT WOOT, so I like to visit him, and this will be my last visit with him. Nuff said about that. Secondly, I’m planning to talk to him about plastic surgery and the hypothetical referral that I was given by someone that I cannot recall right now (I think it was he the surgeon, but could have been my family doc). Bottom line is since I don’t know who said they’d refer me, or who they said they’d refer me to, I haven’t been able to follow up, and therefore I don’t know where I’m at with the referral. This is my life. Just ask my secretarial staff. 

I digress. Why do I want a referral? Two reasons:

  1. My chest wall looks like sand dunes. I don’t need breasts, but I’d prefer tabla rasa rather than a Dali-esque distorted chest wall. Who cares, you might ask? Well, I care. When I wear clothes that cling I don’t care that I’m “flat chested / non-breasted” (the name of my imaginary post-retirement company that sells bathing suits with no cups). But I don’t want clinging tops that show the deep tracts of my scars. That just looks wrong. Troughs across my chest are not a great look. 
  2. I want to have some tatoo work done on my chest WOOT WOOT and I’m thinking that the “memories of boob” bumps could impact the design options. (But what do I know about the effects of bumps on tatoos…)
See what I mean?

So ya, I want to see a plastic surgeon. Can she (yes, she’s a she, I remember that much), … can she do something easy to flatten me out? What about the one deep sink hole? That thing is just going to look worse as the years pass, I can tell you that. 

Belly button #2 and portacath bump in upper right. Vogue material right here. 

You can see why the surgeon appointment is an important DONE for me – because it’s a done with a twist. Done with him, and on to surgeon #2. WOOT WOOT!

Final Treatment

This one is a clear DONE. My treatment regimen was 12 chemo treatments (in a row, so once/week for 12 weeks) and 18 Herceptin treatments (once every 3 weeks for a year). I had to miss one Herceptin treatment because of the heart attack, so that’s why I’m finishing 3 weeks later than prescribed. No biggie.

I’ve been counting down the treatments since the summer, each time taking the nurses the same number of treats as treatments that I have left. So it’s become a bit of a “thing” for me. I started with 13 dipped oreos, then 12 muffins …

…11 drinks. You get the idea…

I really love the nurses in the chemo suite – they’re all so welcoming, positive, gentle, nice… (even the one who I had some reservations about once – I’ve kept my eye on her). Because of the nurses, the chemo suite becomes a safe place to be when you’re in treatment. People are in various stages of feeling shitty, and the nurses treat their patients like family. It’s a nice, calm place to be, and I actually enjoy going. I know that sounds whack, but it’s true. Warm blankets, understanding and a couple of cookies go a long way. 

I can’t say that I’ll actually miss going, but it does feel kind of like the end of summer camp. I have to say goodbye. To make it easier, and to thank them for getting me through it, my good friend Annie is coming with me and bringing a whole bunch of her gorgeous charms that she makes out of recycled glass. I’m going to have each nurse choose a charm for her necklace or bracelet. I’m excited to say thank you that way. I think they’ll love Annie’s work. WOOT WOOT!

Are you surprised that we’re friends? 

Truly though, I won’t feel truly DONE till …

Portacath Removal

I get this sucker out one week after my last treatment. Take a look at this video – it gives me video envy! I have no idea how that woman got permission to video the removal of her portacath, but I’m seriously jealous!! It’s so cool to be able to see what’s being done to you. 

portacath
I am seriously looking forward to this coming out, even though I was offended that I’m not allowed to drive myself home afterwards. I mean, what’s the big deal?

Having the portacath has been a huge asset. It has been so easy for the nurses to deliver chemo and Herceptin. I have seen some of the other patients’ struggles with collapsed veins, and I’ve felt so grateful for my port. It was also super handy when I had morphine injected straight to my heart while I was passing that GD kidney stone! The relief was literally INSTANT (jazz hands here). 

Many people will tell you that cancer is a “journey”. It’s true, it is. My journey is almost DONE. It’s about fucking time. 

Portacath

Port Me

Tomorrow I am going to have my toxic drug portal installed. It will deliver all of the nasty chemicals to my cells without any fuss or muss or burning skin. Ahh. How nice! It’s called a portacath, meaning a portable catheter. It’s made up of two parts: a small disk (port) and a long tube (catheter). Hence the name. 

Port-a-cath

Where does it go?

It will be inserted in my chest, just under the clavicle. Each time I go for a treatment – whether it be for the 12 doses of Paclitaxel (chemotherapy) in the first 12 weeks or the Herceptin (the targeted therapy) in the remainder of the year (18 doses) – the drugs will be delivered through the portacath. Nurses can also take blood through the portacath, even though my veins are quite charming and easy to take blood from. 

Giving blood
I think the nurse had performance anxiety. I can’t recall ever having had a drop of blood spill – or it hurting. Serves me right for taking a picture. 

How is it put in?

Usually this procedure is done in Surgical Outpatients and I would be knocked right out, requiring that a breathing tube be inserted. But as I’m obviously an early adopter, I’m having it done in the Diagnostic Imaging department instead with “twilight anesthesia” (yes, I’m the very first one). This means that I will be in a semi-conscious state. No pain, no anxiety, no need for a breathing tube, no memory of what happened. (This last part is unfortunate, because I’d really like to watch if I’m going to be semi-conscious. I have many questions.) 

In fact today during my teaching session (in which someone tried to teach me…) I asked the nurse how it’s done and waxed on about my vision of the procedure. She gave me a blank look. All she said was “There are 2 incisions.” Blew apart my whole vision, in which … of course I’m going to tell you … I think that the tube is inserted first – it looks like it has to run up and over the collar bone and then down into the Superior Vena Cava. (Remember that one from Biology class? It’s the large vein that runs in to the heart.) The disk is then attached to the tube, and slid under the skin. A couple of stitches later and it’s all done. But likely that’s not how it happens. If I come out of the twilight I will let you know what I see. 

Here is a professional diagram, proving that I am likely very close to being right. 

Diagram of Port-a-cath

How does it work?

Once it is in my chest, each week the nurse just has to poke the special needle through the skin into the top of the port and start the drip. It’s not inconvenient like a PICC line, which is inserted in the arm and has an external port that you have to look after. Apparently I can sleep on my stomach (although I’m not sure if it will be comfortable) and I can swim with it (you can’t with a PICC line). Plus it will make me look like I have an alien microchip implanted in my chest, and that’s cool. 

Bump in chest
See? Cool.