Chemotherapy is OVER

DONE! WOOHOOO! AHHHH! YEAH BABY! YES YES YES! OKKKKAY! And a big thumbs up! Ahhh – no cause for another infamous swearing streak, today is only for happy words. HAPPY! JOY! RELIEF! RELEASE!Mom and I went in for chemo today. The hospital called our house at 7.30 am inquring whether we’d like to push our appoitment forward. Seven thirty felt a bit too early, so we arranged it for sometime before 11. “Any time before 11.”

So, at about 10 am we rolled into the deluxe chemo clinic. Again, things went well. That is a pattern I’m glad to have maintained during the paxlitaxel. The nurses seemed in a fine mood (but they would, as of the 25th they’ll have a 4 day weekend), one was even dressed in red with an elf hat. Very festive.

Chemotherapy took two and half hours, pretty normal. Afterwards the nurse removed my picc line. Let me tell you – removing a picc line is no big deal. Inserting the thing is a procedure (needles, x-rays, heart a pounding – though worth every second) so comparatively this was a walk in the park. Here is what they do: a heat pack is placed on the arm to ‘relax the vein’, the picc bandage is removed, and then the nurse gently pulls the line centimetre by centimetre till out, after which she presses down with gauze for a few minutes so the hole seals and no air can enter my body. Actually, I only realized half way through that she was pulling the tube from my vein. It was hardly noticeable. Why can’t all procedures be like that?

After my arm was released, we packed up the standards (oranges, pretzels, sweater) and GOT OUTTA THERE. Eighty sixed it – outtie five thousand – see you later alligator – hasta la vista – let’s blow this pop stand – I’m gone! High fives for everyone.

At the house Mom and Dad had a surprise gold star waiting for me. It’s a helium balloon in the shape of a star and is currently floating beside their bed. Pretty clever. Also there were lovely gifts from a few friends, and that was a wonderful surprise too.

Now I’m in the kitchen. Daniel and JP dragged the mattress upstairs so I could sleep yet still hang out. I’d tried sitting in a chair before but ended up sliding my tired ass onto the ground for a nap. This, clearly, is better. Mom just finished making red onion preserve and Daniel is sterilizing some jars. There’s festive music in the background and I’m sitting (sleeping) pretty. Lovely.

Sixteen down and no more to go. Over. Good bye Chemotherapy. Let’s never meet again. Never.

Next up is a vacation, followed by radiotherapy. After that it’s all about reclaiming my life. We’re starting now, which is a great reason for my being here. Marcelle is making sure I eat properly, Tony is treating me, and JP is putting me through a chemo-recovery routine.

If Zsolt were here it’d be absolutely perfect.

About 15 treatments ago I looked at the chemo schedule and thought, ‘how can we get through this?’ Talk about your obstacles; treatments felt like an uphill battle. But look where we’ve gotten – look at the view from the top of this mountain. Big goals were set (are set), and afterwards life became about the baby steps. One week at a time and you can survive. Survive to thrive. This next part (after the radiotherapy) is all about getting better.

I’m so thankful for everyone’s support. Thank you thank you thank you. Your thoughts, prayers, words, and food have been wonderful.

Right – time to lay down. Someone break out that cake! WOHOO!

First is over

Okay. One treatment down – ticking that box off right now.

I think for anyone about to experience chemotherapy, it’d be really helpful to hear about the first experience. Now, I cannot tell you about  the side effect because I only just received my chemo, plus also I want mine to be absolutely minimal – so minimal that I have nothing to write on the subject. We’ll see.

Anyhow – it was a longish day. We arrived at the clinic at 12, just in time for my appointment, and took a seat in the waiting room. Two hours later I went into the treatment room. We left at one point to have some lunch, because the consultant advised that it’d be at least another hour of waiting.

Today the room wasn’t quite so crowded. Apparently they’d had a backlog, but I think it was clearing by the time I was admitted.

I sat down in chair number 5 – so that was as expected, and then I was met by my nurse for the hour. He was quite good, reminded me of a friend from home. The nurse explained my treatment and showed me the syringes. . . one was dark red, the other clear.

First he gave me some anti-sickness drugs, which are helping, so I swallowed those no problem. And then we started the chemo. Basically they put in a canula and start with saline solution. It’s a breeze. Then the nurse gets comfortable and begins with the first injection. It’s not too difficult, they feed it very slowly into the vein. The first drug is the most powerful, so there was some slight stinging occasionally in the vein, but we stopped whenever that happened and let the saline run.

Mid way through I had to visit the loo- and as promised my urine was koolaid red. Gross. And amazingly the drug made its way to my bladder quickly.

Quick aside: I’m sipping on ginger beer and think it’s powerful stuff. Whew! The explosion of ginger!

Next came the second drug, this one clear. It was easier to have this given to me – no stinging pain, though it did make my head feel a bit drowsy.

And then that was it. All over. Not so bad.

Of course, I had decided to try the Zolodex for this month, so all this was proceeded with an uncomfortable shot into the stomach by a very lovely nurse. Zsolt’s hand may have been damaged in the process, since I sized it like a vice as the needle just kept going. Eugh. BUT we’ll see what happens next.

Now I’m at home, writing this blog. Truthfully I am starting to feel pretty darn tired, and my stomach feels rather bubbly. Optimistically I had Zsolt run out for pizza, but realistically it’ll probably be boiled rice tonight. Also, need a bit of fibre to help everything move along.

Anyhow – I am alive and fine and coping. Thanks for all the texts, and the good thoughts.

Time for bed!

After the mastectomy

Today is Zsolt’s 29th birthday. He’s a fine kind of man and getting better every year. In the morning I serenaded him with  multiple rounds of happy birthday, followed by some birthday crepes (made by Zsolt with my help), presents, and a game of football. England vs Germany – at this point things aren’t looking hot for England because Germany just scored their fourth goal. Brutal.


Later today Zsolt will make us some birthday quesadillas while I cheer him on, and we’ll have some cheesecake that my colleague’s wife bake especially for Zsolt. It’s looks really delicious and is sitting in the fridge just waiting to be eaten.  Overall this isn’t the birthday we expected, but to be together is enough.

Tonight my mom flies out from Ottawa and will land tomorrow morning at Heathrow. She’ll be here  early afternoon-ish. Thank goodness for that; I can hardly wait to see her. Processing this away from home can distance me from those sad emotions, but not being able to hug my family sucks.

So – after the mastectomy, as promised. If you don’t want to read a long post I’ll give you a quick, poetic-type summary:

After the mastectomy – short version, by Catherine

Groggy, sleeping, blood pressure, needles, pills, waking, washroom hurdles, drinking, vomit, drinking, needle, waking, talking, sitting, bored, sleep, Zsolt! taxi, bed, painkiller, painkiller, numbness, stiff arm, stiff neck, missing breast, don’t look, look, don’t look, look and finally get up, get out, get on. And eventually back to bed, because I’m still a little tired.

After the mastectomy – long version, by Catherine

So it’s been okay. Thank goodness I’m out of the hospital.  Did you know it’s nearly impossible to sleep in a hospital? Forget about sleeping well, every moment of dreamy bliss is quickly taken away by an alarm, a neighbouring patient, or a visiting nurse. Of course, they’re just doing their job and considering how low my blood pressure was, I very much appreciate that.

After Zsolt was asked to leave the ward I drifted off, but was woken soon after for a blood pressure check. Attached to my catheter was a drip, which helped me stay hydrated because I couldn’t keep anything down. It was a slightly messy night with details I won’t mention, but I must give a shout out to Lou in the bed opposite who pulled my curtains shut and handed me a tissue when the nurses couldn’t attend.

The staff was busy, but still very supportive. And thank goodness for that midnight shot in the butt. It was a big needle, but stopped my nausea cold. I don’t even know the name of the nurse, but I really appreciate her care.

The following morning I had a visit from one of the surgeons. She didn’t do the operation, but she had been there to assist. Apparently everything went smoothly; I should have one neat scar across the right of my chest. Actually, she was very friendly and informative.

Then I was visited by one of the breast care nurses. She explained my upcoming appointments (consultation in 2 weeks, they’ll examine the lumps and see how weak/strong the cancer is), and gave me a little additional information. I’ll be fitted with a silicone breast in about 6 weeks time, after the scar has healed more.  Also she warned me to moisturize my arm and hand, to wear gloves around chemicals, and not to get any cuts in my right arm because without the lymph nodes I’m at greater risk of illness in that area.

Finally Zsolt arrived, and we were both visited by another nurse who checked out my bandages, which I didn’t look at, and gave me some exercises. Also I received two comfys, which are soft fluffy forms to slip into my bra. Frankly, a bra is totally unappealing at the moment but it’s nice to know I have spare boobs available.

Pain wise it’s not bad. There is a numbness beneath my arm (because they removed the lymph nodes) that is slowly changing into a tingle. But no – I’d say a paper cut with its shocking sting is more painful, though less constant.  However this is my fucking breast so ultimately a paper cut doesn’t compare; stupid example.

Point: it’s not too painful.

Comfort wise it is different. I feel like something is constantly pulling on my side and the numbness is a bit disturbing. Also there is a drain in my chest, which leads into a long tube, and down into a container which Zsolt empties once a day because I can’t stand to watch. I’m leaking fluid and blood. Gross.

Body wise it’s a shock. At the hospital I never looked down. At home I was crying when Zsolt helped me change shirts. The uneven slant of cloth across my chest is bizarre. I miss my perky peaks; now it’s all downhill.

However, today I didn’t cry, and I didn’t freak out. This is my chest and I’ve got to accept that. And I think that once the discomfort stops, I’ll really be able to adapt to my new look. I still look forward to visiting the beach, and I still look forward to wearing pretty dresses with v-neck tops.

Bottom line: I still love my body.

That is after the mastectomy, as promised. Anyone about to undergo the procedure – all I can say is have a chat with yourself, know it’s the best and just get through. Everyone reacts differently to losing a breast, but we all come through it. And it’s better on the other side. This cancer is out of my body, and even if anything remains  – I’m going to blast the shit out of it with treatments to follow.

So here’s to the first step. And here’s to Zsolt, my new carer and 29 year-old hunk. Happy birthday Zsolti, I couldn’t have managed without you.

Cheers!