Friday, 27/11/09

Chemo: Round 3

> After hospital, My life! — Jane @ 15:47

I started back on chemo yesterday.

The pain I’ve been getting in my left hip area has been increasing of late, so after speaking with Dr Hofmann it was decided that I should try having a lower dose of Oxaliplatin at weekly intervals. Way back in February of this year, I was taken off Oxaliplatin because I was suffering several side-effects, the most serious of which was larygngeal spasm: not something I can recommend. However, we discussed possible options, and it was decided to lower the dose dramatically, and to place me on prophylactic steroids and piriton prior to having chemo, in the hope that this would help. Needless to say, everyone was a little twitchy as the infusion started, and Paul was on standby, hovering over my buttocks with adrenaline, just in case!

Thankfully, no reaction, so the problem seems to be dose-related, rather than a sensitivity reaction. Of course, we are not totally out of the woods yet as the drug will accumulate over the next weeks, so we’ll see what happens as the course progresses.

But maybe we’ve just bought me a little more time, for which I am eternally grateful :-)

Wednesday, 2/09/09

Chemo: Round 2

> After hospital — Jane @ 15:59

Just home from the second round of chemo. Dr Hofmann (oncologist) came to see me before I started, to find out more about the symptoms I had experienced last time – all of which had been much worse than at any other time. So, it was decided that I would have a syringe driver attached to administer Cyclizine (an anti-emetic AND anti-psychotic, just to cover all bases!) over the next 48 hours. Which means I have the portable pump going in to the PICC line in my left arm, and the syringe driver attached to my right arm – all of which makes life very interesting!

Not to worry, it seems to be doing the trick, and I don’t feel anywhere near as nauseous as last time.

Dr Hofmann also called to see me before I left for home (that’s never happened before, so she must’ve been concerned about me), and in addition to asking how I felt, said that the genetic test results aren’t back so we are still in limbo as regards incorporating the additional chemo as we blast the cancer cells.

On a joyous note, I have had a happy few days as friends called round with early birthday cards and presents, realising that I may not feel in the mood to celebrate tomorrow. We took in a selection of drinks and chocolates (not that I would ever condone the imbibing of alcohlic beverages or the consumption of sugary treats) for the chemo nurses, so that they could celebrate on my behalf. They all seemed to have an extra skip in their step as they went about their work today… :-)

Thursday, 20/08/09

Return of the Toxic Woman

> After hospital — Jane @ 08:08

Yesterday I had my first round of chemotherapy, so now I have returned to ‘Toxic Woman’ status.

If you missed my original post about chemotherapy, you can read it near the beginning of my blog, entitled “Tell me why – I don’t like Mondays.” I now need Sir Bob to bring out another song called “Tell me why – I don’t like Wednesdays” because yesterday was pretty grim.

I had spoken to the oncologist on Monday about prescribing me something different to help with the intense nausea that I experience (I had decided to take to heart her words “Stop being brave!”), so was given Aprepitant along with Ondansetron. If that’s the good stuff, I’ll stick with the bad stuff. In addition to feeling so sick that I had to come home with a just-in-case bowl (that’s never happened before), I had the headache from hell which meant that I took to my bed and didn’t move (apart from very, very carefully getting changed) until 7am this morning.

The only advantage I could see was that I did at least sleep rather better than usual on chemo night – a small price to pay for feeling so ill.

On a happier note, it was good to meet up with my old comrade-in-cancer, John, yesterday morning. He’s 67-years old, as fit as a butcher’s dog, and sounds to have had his bowel tumour successfully removed. With a bit of luck, he should finish his mop-up course of chemo in a few weeks, and then he’s on review. Our paths have intermittently crossed, so it was very good to hear his positive news.

No doubt he is just returning from his early morning 5-mile walk, whereas I am just returning to the land of the living. But at least I have been able to eat a light breakfast, which shows a definite improvement after yesterday.

This too will be endured :-)

Monday, 17/08/09

More chemo

> After hospital — Jane @ 20:00

Today I had appointments to see both the colo-rectal surgeon and the liver surgeon.

First, it was off to Huddersfield for a chat about how my colo-rectal surgery had gone. The surgeon was very pleased, and even suggested the liver surgeon could reverse my stoma when he did the surgery next month. All very upbeat.

Then I went to Leeds to see the liver surgeon, and the news wasn’t so good. The MRI scan has shown that I now have 16 sites in my liver, so he won’t now be doing the surgery as previously planned. Instead, he had just come off the phone to my oncologist, and I go to see her first thing in the morning, with a view to starting chemo again some time this week.

All of which means it’s a good job I didn’t pack my suitcase, as I won’t now be going to Edinburgh.

This too will be endured…

Tuesday, 7/04/09

Tell me why – I don’t like Mondays

> My life! — Jane @ 08:04

Off to the hospital at 9am to have my bloods taken prior to chemo. Levels OK, so back home for a couple of hours whilst pharmacy get their act together and mix up the demon brew.

Start chemo at 1pm with premeds of Ondansetron (to combat the nausea and vomiting) and steroids (which will keep me awake all night). Then we get on to the ‘Elixir of Life’ with the first infusion of Irinotecan. This takes about 40 minutes to drip in, and I know after 15 minutes I’m going to become lightheaded and lose the ability to concentrate. No chance to read as the letters won’t stay still on the page, so I stare fixedly into middle-distance, where things seem a little calmer. Then the hot and cold sweats start, and I have to concentrate really hard if I want to answer anyone, as my speech becomes slurred if left to its own devices.

Asked by the nurse if I want a subcutaneous injection of atropine but I refuse as usual, figuring my body doesn’t need any more drugs pumping into it, and so I’ll just put up with the side-effects for the next hour. Paul sits holding my hand, and we both keep glancing at the clock to see how much longer it’s going to take before the flush through with saline can begin.

After an hour I feel well enough for Paul to leave, and the infusion of Folinic Acid starts. This takes 2.5 hours to drip in, so I pass the time by trying (and failing) to do the cryptic crossword, and by doing the Nintendo DS Brain Training game. Anything under a brain age of 90 whilst on chemo I accept as a minor miracle. Today it is 31, so not too bad.

By now, the queasiness has started to kick in, so I begin my mantra: Stay strong, Jane. This too will pass. Break the monotony by trundling with the IV stand down to the bathroom. There I catch sight of myself in the mirror. A wraith stares back, so I decide not to repeat that exercise again for at least 24 hours. Listen to a CD, working out that if each track is about 3 minutes long, then in 10 tracks time Paul will be back, when we can connect the portable chemo pump to the PICC line, and I get to go home.

Home to a bowl of soup – anything else feels like tackling an elephant, as I’m now acutely aware of the feeling of a lead weight in my stomach and a lump in my throat which means the Ondansetron is battling to stop me being sick. Drag myself to a chair, and sit in front of the TV to pass some time before going to bed. I now have the full-on ‘chemo look’ – deathly pale with only the black veins showing on the back of my hands. Paul comments that the vampires have had me, and it feels as though he’s not far wrong.

Although I’m exhausted I know I won’t sleep much due to the effects of the steroids. I have a couple of books to read – both very light on chemo night – and my radio to listen to if needed. After a chapter of a book I feel so nauseous that I abandon that, turn off the light and try to sleep.

Look at my clock a little while later, and am surprised to find it’s 1.21am. I’d heard Michael go to the bathroom a little earlier and wonder if he’s still there (two hours is not inconceivable, but not usually in the wee small hours). Relieved to find him no longer there, which must mean I nodded off at some point. I pick up the book again, but still too nauseous to care, so switch off the light.

Hear a car going past the end of the road, and wonder who on earth would want to be out at 2am. It briefly crosses my mind that it may be our Minister and his wife, as their daughter, Kerry, is expecting their first grandchild. Maybe Peter and Jane are starting the long trek south to Colchester to visit them. An uplifting thought for the early hours.

The silence is permanently broken just before 6am by a robin, hurling out his challenge to a sleepy world. He is joined a little later by a pair of blackbirds, who have a duel outside my window, and then by the collared doves and wood pigeons. I strain to hear the nuthatch and the greenfinch, but either they are too far away for me to hear them, or they are still tucked up asleep on a branch. It’s strange to think that what we perceive as melodious birdsong is really a battle ground in full swing: this is my patch, so stay away!

Decide to add my own call to that of the birds – Stay strong, Jane. This too will pass – and so with mantra and dawn chorus we enter Tuesday morning….

Saturday, 4/04/09

Blog: Day 1 Chemo: Day 69

> My life! — Jane @ 14:33

Welcome to my blog!

I didn’t know I was going to become a ‘blogger’ but Peter suggested it would be therapeutic, set it all up for me, and so here I am.

If you’ve found your way here then you know exactly what’s going on in my life right now. This blog is going to be my way to keep you updated with where I am in my treatment, and will also give you a chance to leave your comments – even if it’s only “Stop whingeing, woman!”

Today I’ve had a visit from Elizabeth, who brought me a copy of one of my all-time favourite musicals, “Calamity Jane.” So now we’re all a-hootin’ and a-hollerin’ around the house, singing “Whip crack away”, and slapping our thighs!

Monday brings Round 6 of chemo. Hopefully this will be the last round, but that will depend on what the CT scan on the 14th reveals, and what Dr Hoffmann decides on the 20th. Fingers and toes crossed on that day, please…