• October 2026
    S M T W T F S
     123
    45678910
    11121314151617
    18192021222324
    25262728293031

    It’s Day 5 and I’d hoped to start feeling better now I’m past the days of extra medication, but it seems that’s backwards: I’m guessing now they were actually cushioning me a bit.

    In news that will be no surprise to anyone, this isn’t fun. My taste buds went on holiday in time for dinner last night, so all I have at the moment is texture and temperature. I’m tired, queasy and a touch short tempered, but otherwise surviving.

    It’s a nice sunny day, I’m doing nothing but resting, hopefully Day 6 will be better when I get there.

  • October 2026
    S M T W T F S
     123
    45678910
    11121314151617
    18192021222324
    25262728293031

    3 medications, 2 sunburnt cheeks, and 4 hours of insomnia.

    Day 3 is proving rougher than day 2.

    Yesterday I worked a little in the morning then needed a rest. I would then have been fine to go back to work for a bit but it was getting too close to my district nurse appointment so there seemed no point.

    The 4th medication is a syringe and is to be taken 24 hours after chemo. I can self administer but for the first time the district nurse has to watch to see I’m doing it right, and then give me a secure disposal bin for the needles.

    I had had a txt exchange and landed on 11am as my appointment time. I arrived 10 minutes early to discover that they now work out of the medical centre, no longer out of the old hospital where I saw them earlier in the year. Thst was okay, I had time, but of course the medical centre was busy.

    The receptionist had a list of district nurse patients but my name wasn’t on it. She said she’d let them know. At 11:45 the nurse came out to see me and said I was booked at 11 but for Thursday, not Wednesday, and while she could squeeze me in she wasn’t able to do this particular procedure I needed to see her colleague who was currently out doing house calls. By now I needed another lie down so I rang and left a voice message and went home.

    She rang back and booked for 3, back at the old hospital, though she insisted it could wait a few days. I rang the chemo nurses who agreed it would be okay to wait an extra day if I had to but they had put through the urgent referral because the oncologist had scripted it to be given on Wednesday.

    I went at 3, and apart from another argument over the urgency, it got done in 5 minutes. I think the problem stems from the terminology. When I had surgery, that was Day 0. Same if you test positive for covid, the first day of symptoms is Day 0. But for chemo it appears that treatment day is Day 1. I reckon the referral said Day 2, i.e. the day after, but the district nurse was counting from 0. Anyway it got fone, and I still had the energy to do some quick grocery shopping on the way home.

    Back to today, one of my medications is nicknamed ‘Tyrannosaurus Dex’ by the chemo nurses, and they recommend taking as early in the day as possible because it causes insomnia. Well I took it early yesterday but still lost 4 hours sleep overnight. No nausea in the night but it turned up while eating breakfast which I must do before taking Dex.

    The sunburn is a side effect of the chemo itself. I’m not likely to get a tan but I’ll be rosy cheeked.

    It feels like I’ve had a long day already and it’s only just coming up to 9am, but I’m going to try working for a bit, resting when I need to.

    It seems treatment week is going to play havoc with my leave balance but oh well, health comes first.

  • October 2026
    S M T W T F S
     123
    45678910
    11121314151617
    18192021222324
    25262728293031

    That’s one less dose to do!

    We arrived just after 9 for the 9:30 appointment so in plenty of time. The staff were all very welcoming and soon I was in a comfortable chair with my crochet and a fresh cup of tea.

    Then the waiting started.

    First the oncologist wanted an ECG done  and to see the results before we went ahead. Then there was a trip over to the main hospital building for another quick scan as a baseline before starting.

    Next, starting about 11:30, I had to be educated by the nurse on all the possible side efects and which medicine to take when. There are 6 different ones with different instructions so it took awhile.

    Finally ready, they started trying to put the line in. For this medication ithas to go into a vein but not at your elbow. My veins proved unruly, so if it hadn’t worked on the fourth try we would have had to go back into the main hospital to do it under ultrasound, but it did work.  I’ll be remembering that vein for next time s I feel less like a pincushion!

    On the up side, the dose itself took less than an hour then we were free to go.

    I slept most of the trip, got out of the car and slept again, woke for dinner and slept again pretty much through to getting up at 5:30.

    I don’t currently feel sleepy but I am a but lethargic and one of the pills I just took says it’ll make me sleepy, so it’s goig to be an interesting day. I have a little nausea, but I did get through breakfast and that’s mostly what the medication is for so I’m hopeful it’ll work.

    That’s it for this update but wen I dd the flowers the other day I mentioned that the native iris wasn’t in bloom. Well now it is. Pretty, isn’t it?

  • October 2026
    S M T W T F S
     123
    45678910
    11121314151617
    18192021222324
    25262728293031

    Hi Damon here just an update Charlotte will do her own.

    The treatment in thames took 45min, most of the day was other checks, finding veins for IV line

    Got back in the car 2.30 and heeded stright home, Charlotte sleeped the whole way. Straight to bed at 3.45

    Have got her up at 6 for some tost and medications then back to bed

    She can fill the detail in later.

    By for now

  • October 2026
    S M T W T F S
     123
    45678910
    11121314151617
    18192021222324
    25262728293031

    It’s officially winter now but our garden doesn’t seem to care.

    I already posted photos of the hibiscus, so here are some of the other flowers popping up. I don’t know what they are, generally, other than pretty. I’ve captioned the ones I do know.

    Aloe vera
    Orchids, a bit ran and wind damaged

    As for fruit, well our couple of surviving cherimoya are still growing and still rock hard so not ready to harvest. They’re stunted but when they soften they should be tasty.

    Then there’s the orange tree which is heavy laden.

    The fruit are almost ready, we’ve started eating a few. When they’re ripe their flesh is quite dark, almost like a grapefruit, and sometimes streaked with red like a blood orange.  Here are two side by side for colour comparison.

    Either way they’re tasty.

  • October 2026
    S M T W T F S
     123
    45678910
    11121314151617
    18192021222324
    25262728293031

    It may sound silly, I mean I know I am on a cancer journey, I’ve had major surgery, I’ve been bouncing between scans and medical professionals for that very reason, but I just don’t feel like someone who has cancer. What’s that supposed to feel like? I’m not sure, but most of the time right now I feel quite normal and that surely isn’t normal with cancer? Is it?

    Well anyway, yesterday I met my new oncologist. Or, as it turned out, oncologists because I have two: Emma and Sarah. Sarah is the senior oncologist and I spent more time with Emma but at future appointments it’s likely to be one or other rather than both. It does mean if one is bisy or away there’s always someone around, which is nice.

    The latest scan results still show no sign of spread into any organs or muscles, and that’s important because that’s where sarcomas like to live and spread. That’s pretty much what these scans are for, to watch for that. So far so good.

    That said, there is something going on in my lymphatic system. It’s not where sarcomas generally go but mine did. I had 5 lymph nodes removed in November’s surgery and that means the ones left are having to work harder, and that could be the full explanation of what’s happening. Still, out of an abundance of caution, my oncologists are being particularly vigilant.

    Long story short, we’re going to try a round of chemotherapy. It was offered, not pushed on me, and it may have no effect on the lymph nodes if the changes aren’t to do with cancer to begin with, but I think it’s worth doing. I was told back in November that the testing proved the cancer is still somewhere in my body. It hasn’t made itself visible so far, but I’m in favour of giving it a shove back anyway.

    I’m not looking forward to this. I’ve just got life back to normal, and I could have said no, we don’t even know if we’ll be able to see if it’s having an effect.  But I’m mentally ready for it, and I figure getting through it in winter means I should get a nice summer, so that’s something to look forward to.

    The details of when it starts haven’t been figured out yet, but likely before the end of June, running for 18 weeks with treatments every 3 weeks so I have recovery time between. There’s no point trying to guess what impact it’ll have on me, it might be really rough or I might sail through, but the two things I can expect are nausea and lower immunity, so I might be more inclined to linger at home. Which I don’t mind, there’s plenty of crafting to be done.

    I’ll update as I get more details but for now I’m continuing on and going to enjoy each day as it comes.

    I suppose I might now at least feel like a real cancer patient at last. 😊

    Last minute edit: as I was about to post this the phone rang and I have my first treatment date: 16 June. So here we go.

  • October 2026
    S M T W T F S
     123
    45678910
    11121314151617
    18192021222324
    25262728293031

    It’s almost the first day of winter, and certainly we’ve had the odd cooler evening and chilly morning but overall it’s been incredibly mild.

    Right now, mid-morning I’ve just been for a walk in short sleeves on a sunny day. Amazing.

    Perhaps our change in altitude helps. It would have been a damp, chily morning down on the flat today. Look at these two photos, one from 6:30, the others from 7, and town is invisible, blanketed with low cloud.

    6:30, with the aid of the camera flash which makes it seem brighter than it was, no sign of town
    7am, no flash needed, still no twn but it’s lifting, you can see a little more of the trees and shore between our neighbour’s and the tall trees at the bottom
    7am, the sun is up but hidden behind the ridge for us

    By comparison, here’s a morning view of town from a few weeks back

    The sun is also behind the ridge in tbis photo

    In the garden things are still growing and blossoming. Here are some recent photos of a handful of our hibiscus – we have about a dozen, all in different colours.

  • October 2026
    S M T W T F S
     123
    45678910
    11121314151617
    18192021222324
    25262728293031

    Two weeks after the lst scan I finally have a date for my next oncologist appointment: 4 June.

    Given the casual nature of the conversation I had with the bookings clerk (who was going to ring sometime in the next fortnight to make an appointment if I hadn’t rung her first), I can only assume they saw nothing upsetting in the scan results, which is a positive thing.

    My Auckland oncologist, Michelle, has referred me to the public team in my own region, which should mean shorter trips overall and also it’s free rather than seeing her on my medical insurance and paying the shortfall, but I can still contact Michelle if I’m worried about anything.

    According to the appointment letter my new oncologist will be Sarah, though it also says ‘or registrar’ so we’ll have to wait and see. I have to go to Hamilton for this first appointment but after that apparently appointments, scans and treatment can all be done in Thames which is much more convenient.

    It’s good to have a date. Another full day of travel but then shorter trips after that sound very good.

  • October 2026
    S M T W T F S
     123
    45678910
    11121314151617
    18192021222324
    25262728293031

    The weather this weekend was great and we made good use of it.

    My clotheline area is now cobbled, so no more walking on the dewy grass.

    My husband and father-in-law levelling th ground
    Halfway done, stopped for a cup of tea
    Cobbles are done so the washing can finally get out

    The washing got out mid afternoon and surpriningly all but three items did get dry before we lost the sun for the day. Impressive for the time of the year.

    While the boys were busy cobbling, I was alternating between, cooking, dyeing wool, and yes resting as well.

    I was recently given a second hand pie maker, so gave that a go with some leftover beef stew to make steak pies.

    12 steak pies

    I’m still figuring out how long to cook them, whether or not to eggwash the tops, and so on. The machine only does two at a time so it was an exercise in patience waiting for it to cool down beween sets.

    Fortunately I had the dyeing to fill in the gaps. It’s been nearly 18 months since I last did any, and finding all the various bits proved harder than expected as things have gotten scattered. I was hoping to use my avocado and onion leftovers – the the avocado skins and pits are taking up space in the freezer – but those have to be done in two steps for best results and I couldn’t find my alum. We found it on Sunday but by then it was really too late. I’ll do that over the next few weeks.

    So for this time I’m using Ashford acid dyes. I have three colours left over from my last dye experiments in late 2024: violet, orange and coal. I suspect they’re well past when they should have been used but the results show the violet at least is still potent.

    The set up on the front deck while the cobbling was happening out the back
    The result, 4 dye lots in different shades

    Mixing the dyes in different propotions gave me a range of purples doen to a dusky rose. That last is mostly orange with just a little violet.

    I still have yarn left for the avocado and onion dyeing when I get to them.

    8 skeins waiting for dye

    I’ll post the results when they’re done.

  • October 2026
    S M T W T F S
     123
    45678910
    11121314151617
    18192021222324
    25262728293031

    Today’s trip went well.

    For a start it was supposed to be raining but while it was misty and damp, it wasn’t actually raining.

    Town with the clouds breaking up. See the low drift of white cloud over the bay

    Then as I was packing the car, I saw a kereru/native wood pigeon in the neighbour’s tree over our driveway. I tried hard to get a picture without chasing it away. You’ll have to zoom in.

    The road was wet and misty but traffic was light. I’d left very early both for the weather conditions and for the roadworks on Pumpkin Hill before Tairua, and ended up arriving a full hour early. Which proved fortuitous as I was taken in early and was on my way out of town before my scheduled appointment.

    By the time I left it was turning into a nice day in Thames. Still misty over the hills and dreary and wet between Hikuai and Tairua, but from there it was brighter. Here’s the view from the roadworks queue on Pumpkin Hill, showing sreaks of blue in the cloud cover.

    It was beautiful between Coroglen and Whenuakite but then started clouding over again in Whitianga. There were more roadworks just coming into town, so I took another snap then

    View towards town
    Clouds coming over the hills

    It’s rained a little since I got home, but I’m home and it’s warm and the trip is done. Yay.

    No word yet on the next appointment but at least the scan is done.