Tag Archive for 'Port Flushes'

Shirley Has a Beautiful Bald Head

On the mondays between chemo session, such as today, I go to the hospital for blood tests. They want to check my blood to make sure that I’m not tanking too quickly. If my white blood cells were to fall too low, they would put me in isolation in the hospital to prevent possible infections. And that would be no fun.

But I don’t have to worry about any of that right now. In fact, according to the results of my blood tests today, I’m getting healthier and healthier as I go through this process (aka: the opposite of what is supposed to happen). They didn’t even give me a booster shot today.

This past week was, even so, more difficult that previous weeks. It’s starting to get harder to keep up with life. I was really exhausted Thursday through Saturday. People asked me how I felt, and I just didn’t have the energy to feign fortitude.

Today was the first day that I dreaded going into the Cancer Center. I like the people that work there a lot, but I’m getting pretty sick of seeing them. Every time I go there they stick me with something, or fill me with something, or rough me up in some other way.

I met a lady there today named Shirley. Shirley has lung cancer and no hair. She was very friendly. It’s funny how cancer patients will tell each other the most intimate details, even if they are total strangers. She took her hat off to show me her bald head. She was old and feeble, but it was kind of beautiful in a way. I pulled out some of my hair to show her that I’m losing mine, too. She told me about her hysterectomy and I complained about steroids. I reminded her of a National Geographic photographer that she used to know, and I told her that he must have been a very dashing young man. She told me that, yesterday, she prayed to die. I’m glad she didn’t, though, because we had a good talk.

Chemo Port

bardport-space

This is a picture of the thing they implanted in my chest to make chemotherapy easier.

Except my “port” is not orbiting in space, above a beautiful blue earth and purple nebula, as the picture suggests. My port is located under my skin, about an inch south of my left collar bone. A tube connects it to my heart, by way of a big vein in my chest.

It is also *not* the size of the earth. (The earth was, seriously, just not a good backdrop for this promo shot. I guess it’s probably hard to make this thing look cool, though. You gotta throw a nebula or an icecap or something like that in to hip it up.) It’s maybe 1/2 inch in diameter. It’s part of me now.

I also sort of doubt that mine is stainless steel like the picture, I believe they told me it was plastic – although I surely don’t know what the thing looks like under there.

If I didn’t have this port, they’d have to put the cocktail straight into my arm. Getting chemo in the arm is the Dirty Harry, “Go ahead, make my day,” psychopathic way to get chemotherapy, from what I hear. The nurses cringe when they talk about it, as if they don’t like giving it like that anymore than people like getting it like that. Something about blood clots, burned skin, melted veins…let’s not talk about it…

I suppose I’m grateful, then, for this funny looking thing sticking out of my chest. It looks pretty stupid, though. They tell me I’ll have to keep it in for quite awhile after chemo is all over, in case the disease comes back and we need to do this again…let’s not talk about it…

Port Flush Me

I had another port flush on Monday.

Shirley was there. Getting chemo, I think. She told me she loved me. I told her I loved her too, but I sort of mumbled it and had trouble looking at her when I said it. Sometimes I do that. Cancer patients are quick to tell anybody that they love that they do, but I guess I’ve retreated back into the alternative. Maybe I’ve forgotten that life is short. I guess I have.

The hospital has asked me to speak at a survivors function in June. It’ll be held in a ballroom in Elgin and attending by survivors, doctors, nurses, maybe patients, too.

What on earth can I say to a roomful of survivors, oncologists, and oncology nurses that they don’t already know?

I’ll imagine I’ll skip the clinical-speak. Surely they know all the statistics. And I’ll go easy on specifics of my chemo. I suppose they don’t need to know what kind of anti-anxiety meds they filled me with, or how many mL of Bleo they put in me.

I told my doctor about the speech and his only advice was that I, under no circumstances, should talk about him.

So I definitely have to come up with something about him.

I’ve got plenty to say about the shoddy shape of the American health insurance system, but I think I’m supposed to be inspirational, and there’s nothing inspirational about health insurance in America.

I could talk about being a pianist. With a CD out (by then, hopefully). Who needs more piano students. And is available for private parties and restaurants. For $75 an hour. Then I could hand out my card and free demo CDs. And maybe put a bumper sticker on my back that says “HIRE THIS MAN”. I could put up a copy of my resume and rates on a projector. Hand out coupons or something.

Which would be shameful.

No, it’ll need to be something personal. About how I got through chemo and planned on going on a great, inspirational trip to the California mountains. But then I got offered money to stay home, so I didn’t go on the trip, and instead worked 7 days a week to make about 1/2 the money one would need to live comfortably, and then had trouble looking people in the eye when I told them I loved them. And I stopped watching the seasons change, or relaxing long enough to see a movie with my girlfriend, or go to dinner with a friend. And I only replied to e-mails that related to making money. And I ignored medical bills, and racked up my credit card, and ruined my finances, and mostly just became a small person, with small ambitions, and a short wick, who never went anywhere except work and bed.

But that wouldn’t be very inspirational.

Maybe I’ll say how I decided after being diagnosed that I’d never lower my ambitions to anything ordinary, and instead, I’d live an extraordinary life as a musician, and an author, and a friend, and a lover, and a traveler. And even though it is never easy, I know that life is too short to forget my intentions.

But which version is true?

Both.

Maybe I’ll just try not to talk about myself. Maybe I’ll talk about Shirley or Courtney. Courtney – maybe after your surgery today you can do something inspirational, or funny, or cute, and I can talk about anecdotally in June? Just waking up will seem pretty inspirational to me, but we’re talking about a roomful of oncologists here, it might take more than that.

By the way, Courtney, I’m worried about you today.

Comments

Margie: “I am also in the process of getting chemo treatments. I…
May 5, 2012, 5:59 pm
Dale: “Family of cancer patients get the same thing. My mother had stage…
May 3, 2012, 3:58 pm
Renee: “Thank you for sharing. My 2 year old just started chemo 3…
May 1, 2012, 7:47 am
Leslie: “I can empathize. I am going through chemo now and I HATE…
April 30, 2012, 8:32 pm
alanna: “Thank u so much for sharing. Ill be starting chemo either the…
April 30, 2012, 4:58 pm
Judy: “Well, I just had my second of six rounds of Taxotre, Carboplatin…
April 29, 2012, 7:28 pm
delta goodrem: “actress & singer. she is also a judge on 2012′s the voice…
April 27, 2012, 9:18 pm
Sandy: “Thanks for sharing that exactly how I feel. I started chemo on…
April 27, 2012, 5:23 pm
Sarah Yoon: ““Waiting for the show I guess” haha. But you’re quite calm about…
April 27, 2012, 8:55 am
Sarah Yoon: “You actually look quite handsome on the right :) good luck. You’re…
April 27, 2012, 8:42 am
Nikki: “;) it’s true….
April 25, 2012, 5:05 am
Tina: “Thank you for sharing this. My mother starts Chemo soon for Pancreatic…
April 24, 2012, 10:10 pm
Susie: “I am writing a book and one of my characters has cancer,…
April 22, 2012, 1:33 am
Jon: “My dad’s going through chemo at the moment for a mesothelioma. What…
April 21, 2012, 8:38 am
Missy: “Thank you so much for sharing this. I’m so sorry you’ve had…
April 19, 2012, 3:04 pm
Rina: “Thank you for sharing your experiences. My Mom is right now recovering…
April 19, 2012, 10:24 am
Victoria: “I couldn’t read through this. Having had the “pleasure” of experiencing…
April 17, 2012, 8:03 pm
hilary: “aww that sucks thank you for sharing this my best friend has…
April 17, 2012, 5:49 pm
Michelle: “My coworker is not doing well… Hospice has been called. He is…
April 17, 2012, 12:17 pm
Naomii: “My Mum was diagnosed with IIIB last week Wednesday adn I…
April 16, 2012, 5:27 am
Gwen: “Thank you for sharing. I feel the same way. I…
April 14, 2012, 12:11 pm
Taylor E: “thank you for explaining your expierience. my gfs mom is going to…
April 12, 2012, 12:34 am
Nina: “I was diagnosed a few months ago and have a brother and…
April 10, 2012, 6:10 pm
terry tirabassi: “its amazing to find someone who can describe the way i feel…
April 9, 2012, 3:45 pm
Leigh Loree: “Thanks for the information – my daughter just had chemo on Thursday…
April 8, 2012, 8:46 am