Tuesday 26 December 2017

A wonderful Christmas Day (2017)

Christmas Day is over...all that mental running around and stress of what to buy who, what goodies to eat is over for another year. I think I was pretty ok...I pretty much had mine sorted early on and just had to go to the supermarket first thing Christmas Eve to get the fresh goods we needed. So I was there a few minutes before opening...with about 100 other people!!!!! What a crack up! It was a jam trying to get a trolley and it was slow going through the first few aisles but it was completely worth it! I was done and dusted, back home by 9.00am...even stopping into The Warehouse to get myself a sunhat - I was pretty damn happy with myself.

Since my baby girl and her honey weren’t going to be home Christmas morning, we had decided we would do presents after we got home from the beach, so basically it was get up in the morning, put the cold foods and drinks into the chilly bins, load up the car and off we go. Hubby had loaded the car up the night before with the towels, and anything else which was able to be...it was great. We were on our way before 8.00am.

It was just the best day ever! It was exactly what I had hoped for. We were the second ones to arrive (9.00am) (the first ones had stolen our usual area) and we tried to spread ourselves out (all three of us) in the anticipation of baby girls ‘other’ family arriving. The sun was shining, the water was beautiful and sparkly. We had brekky as soon as we were unloaded, and I was off for a swim pretty much as soon as my food settled. It was such a relaxing day...baby girl and her honey and his lovely family arrived about lunch time I think - it was lovely sharing the day with them. A really lovely family...the kids are great - it honestly was such an enjoyable day. Its nice to have little kiddies around on Christmas Day, they make it a little more fun I think. We didn’t leave until 8.00pm so had definitely been there making the most of the day. Hubby went for a walk around the rocks to do some fishing and came home with a snapper (although he didn’t say anything until we got home) and the other guys went diving and the sisters and kids all went for a walk. Nana is in a moonboot, so her and I sat and chatted away. A tough day for her, with being the first one without her husband. We talk often, I’m not afraid to ask questions about how she is feeling because I understand completely. It was nice being able to chat away as my days of being able to do that long walk or look under rocks etc is over. My back can’t handle it anymore but thats ok...I can still enjoy everything else about it. I was exhausted by the end of the day and could quite easily have jumped straight into bed but we waited for baby girl and her honey to come home to open pressies. A nice end to a beautiful day.



I heard my baby make the comment that some of her friends were saying how boring their Christmas Day was and it kind of solidified what I had been blogging about Christmas Eve when I was a kid and how boring I always found it. And I could tell by the way she said it, that she was pleased that we were all having such a good day and that warmed my heart more than anything else. Christmas is such an important day to me, and important it is an enjoyable day for the girls. Obviously it is changing now with them being older and it does sadden me sometimes that we are such a small family but helloooooo, no changing it now...until grandbabies start to appear and my big girl decides she is ready to meet someone. She is happy as she is...

And so as usual, I have come home sunburnt. I really thought I may have finally learnt my lesson and stayed out of the sun and kept my sunhat on all day but it wasn’t to be...I think I need to just face it. I am a sun bunny, albeit an old one now! But the sun is like a beacon to me...if I see a patch of it, I need to be sitting in it. My big girl is also sunburnt which is actually unusual for her. She’s normally pretty good about lathering that terrible stuff all over herself.

Its Boxing Day now. We are all lazing around in bed except my little girl. She had to work today but is happy because she has an early shift, finishing at 2.00pm. I am back to work tomorrow for three days and then another 4 day weekend - woohoo!!!!

And so the chapter ends for another Christmas but will continue to hold lots of good memories. I can finally tick it off my ridiculously small bucket list but honestly I just can’t wipe the smile off my face thinking about yesterday. What a bloody awesome day...bloody loved every minute of it!!!!

Time now for a cuppa and some toast๐Ÿ™‚

Boxing Day 2017 - 10.28am

Monday 25 December 2017

Christmas memories

As we count down to Christmas of 2017 hubby and I were just talking about how yet another Christmas is upon us and how much they have changed. The girls have grown up into young women leading their own lives and for the second year in a row, my baby is away for the night (Christmas eve) and we won’t see her until we meet up at the beach tomorrow. I feel sad in a way, but that is life...she has her own life to lead now, has a young man and another family in her life. Which is wonderful, to know she has such lovely people in her life. All you want for your kids is for them to be happy and for them to  make good choices and my baby girl has done that well. My big girl hasn’t quite gotten that far yet (meeting a young man yet I mean) but she is happy with what she is doing and although she is working until 11.30pm tonight, might be going out with workmates for a little while before coming home...and so she should be...they are only young, they should be going out and enjoying life. Last year the girls went out to a mates for drinks after we got home from their nana’s place where we had spent the day. First time they had ever done that...And  then I think of David and I wonder where he is. Can he see us wherever he is? And I think about the last Christmas we had together before he died.

We were having a quiet Christmas at my sisters place in Glendene...just us with our babies and a couple of my older friends who didn’t have family (we were their family until the friendship got screwed over). David and I, and the girls were supposed to stay the night...it was all organised. And it was lovely - we were all out in the backyard, the kids playing - a perfect family day. The boys had put a hangi down I think...And then some people my brother-in-law had invited over for a drink arrived. I didn’t know them...and so the boys sat with these people drinking and I sat with my friends and the kids and my sister I think was torn...she wanted to be polite to these people or maybe she wanted to join them but because we weren’t joining in, felt a bit awkward. I don’t really know, we never really talked about it. But my friends eventually left and I didn’t want to join in.  With two small babies I wasn’t interested in drinking and so I packed the girls up to go home. I remember my brother in law was quite upset which wasn’t my intention but it wasn’t the Christmas I had envisioned. I think if they had been people I had known, it would have been different..but I just felt awkward so we left...and so we left David there, to get drunk on Christmas night with people he didn’t know. His priority was to get drunk with strangers and not be with his girls. Six months later he was dead...and no more chances for family Christmases and that is my point, you just don’t know what is going to happen. I often think of that last Christmas and how he chose to stay and get drunk. My choice was to go home with my babies. I am sad when I think about it or maybe its more a case of being slightly annoyed that he made that choice but you can’t do anything to change it and none of us knew it would be our last Christmas together as a family.

Christmas has always been important to me, to make sure it was a fun day for the girls. When I was a kid, it was always such a boring day. But thats only because it was just mum and dad, and my sister and I. Poor Mum would be in the kitchen all morning cooking this big beautiful roast with all the trimmings then we’d have a late lunch, my sister I think would usually go to her mates place afterwards and we’d be stuck at home watching TV. As a kid, I could never understand why people were so excited for Christmas Day. When mum was very ill in hospital, dad decided to do a bar-b-q as it was much simpler. I was about 25 or 26 and it was weird, it felt completely strange and the traditional roast was all I had ever known but that was the beginning of a change in Christmas. I think that was mum’s last Christmas. We had all traipsed up to the hospital in the morning to visit her with a rubbish bag full of pressies, took a tape recorder up and the grandkids sang Cliff Richards Mistletoe and Wine...I remember the nursing staff all standing in the doorway of mums room listening, it was so emotional - that song still has the ability to bring a lump to my throat when I hear it.

So Christmas evolves with whoever is around and whatever is happening...for me, it is completely about family and spending time with those you love. I don’t need the presents or the flash food. We have got our picnic food ready to take to the beach and I am happy with it. No puddings to either take with us or to feast on when we get home. The kids weren’t fussed and I am happy to not have to indulge. The kids and I are looking forward to going to the beach. Hubby has mixed feelings about it I know but I really appreciate his just going along with it. He has even got his fishing gear out to take with us so that tells me, he is going to make the most of it and I love that!

So all these Christmas memories have come flooding back and with it has brought our latest Christmas Day to us. Hubby is fast asleep beside me (slightly piddled) and neither of my girls home. I don’t ever want to be one of those mums who clings on to her kids - I want them to go out and make their own life,  not revolve it around me (but please don’t forget me) but I have to admit at times I struggle. Even tonight with it just being hubby and I at home, I was torn between enjoying the quietness and emptiness of the house, yet knowing it is Christmas Eve and that my banies weren’t here.

Even on Friday night we had a few people from work around and I felt very much a generational difference between them and me. I felt like I didn’t belong...I definitely felt a divide between them and me. Certainly not in a personal way and probably not in a one on one situation but as a group, I definitely felt out of place. Yet hubby was there, his younger brother was there and one of my close workmates who is slightly younger than me, was there so it wasn’t like I was the only ‘oldie’. I don’t know why I feel like that. Maybe its just the load I carry on my shoulders...

But hey, another special day is upon us so lets enjoy it - at a much more reasonable hour! I think I can hear simging coming from somewhere, not drunk singing but like a church choir and goddammit, a bloody alarm keeps going off every 10 or 15 mins. Its very faint, probanly coming from one of the girls rooms but it better not keep me awake...sometimes those quiet noises in the dead of night are like a set of drums going off for me...

Christmas Day 2017 - 12.46am


Sunday 17 December 2017

Summertime...

Its a week out from Christmas, the sun is streaming, as I still lie in bed at 10.15am with the windows open and one curtain slightly ajar, enough to let the rays in. Such a beautiful blue sky and you can hear the birds chirping. What bliss...my idea of heaven...I wonder if this is what it will be like when I die - constant sun, blue skies, birds chirping and no getting sunburnt and peeling! Just feeling the warmth embrace you, no having to grab a blanket to wrap around yourself to attempt to keep the chills out...this is my favourite time of the year. I don’t cope quite so well as I used to. Until a few years ago, I would be lying out in the sun whenever I could get the chance, going from a pastie white colour to a lovely brown - definitely the remnants of my Maori roots coming out, from my mum. These days while I love the sun, I have to hide away under shelter, even with thoughts of wearing a wide brimmed hat to keep it off my face. God, never ever has that thought ever crossed my mind before. Still surprises me that its breast cancer which has gotten its tentacles into me and not melanoma and still I don’t put sunscreen on anywhere other than my face...maybe this year - its never too late to learn!

I had my first beach outing yesterday with my big girl and a couple of mates from work. We had planned it a few weeks ago and so I had been keenly watching the weather as the days went by hoping like hell it wouldn’t go from roasting hot to a bloody tsunami or something...as it was, it was slightly cooler than the other days but it was good enough and it was a good day. I have been wanting to do a long-ish drive for a little while now, so it was a great test run, especially considering we will be going back to the same place on Christmas Day. It felt great, I enjoyed the drive although getting frustrated with the queue of traffic for the last part of the journey. Today I am suffering a wee bit, feeling pretty achy but thats what painkillers are for and it was totally worth it. Its always nice to take new people to ‘our’ beach - Martins Bay. We have been going there for years and have a lifetime of memories, starting with when David was alive and pre-kid days.  My ideal day at the beach is to just blob, swim, eat and blob again. I have never been one to play beach cricket or touch and so I hope the girls weren’t too bored. There was a Samoan family on the opposite side of us with their volleyball net up. I know one of the girls was itching to go join them and I was trying to encourage her to go but she didn’t. ‘L’ started working with us earlier this year and right from the start there was something about this young lady that I really liked, so we struck up a friendship and I encouraged a friendship between her and my girls whom all got on very well. I am sad to hear that she will be leaving us to go back home to the Gold Coast but I understand her reasons. It comes back to that saying, people come and go from our lives...some stay longer then others, and others flit in and out. I hope this won’t be the last we see of her...I have definitely felt a protectiveness over her in much the same way as to my own girls. She was saying last night that she tells other people I am her second mum (I love that) and I think people at work (the younger ones I mean) are surprised that she has hung out with me. What they probably don’t realise is that either one or both of my girls has been with us!









This week will be a quieter one thank goodness. I have a couple of things to do today, my baby girl has a few mates coming around tonight for a pre-Christmas get together so will get out to pick up a few things for that. I aim to have plenty of rest so I won’t be exhausted for our Friday drinks with people from work. I have no idea who will come round but thats okay. There are no expectations, those who do come round can stay for as long or as little a time as they want. I am looking forward to it. The younger ones may see me in a different light away from work but even if they don’t, thats ok. In the light of summer, shit like that doesn’t make any difference...thats the difference between summer and winter - the state of mind. That might change when I walk in the door tomorrow morning...

Sunday 17th December 2017 - 11.10am


Friday 15 December 2017

Everything has caught up

Wow, what a week. Actually, what a month! For someone who says she doesn’t go out much or likes to make sure she has down time, to be able to get through another week of work, I sure as hell haven’t lately! There has been catch up’s with people, lunches, dinners, parties and such like...to the point where I pretty much came down with a crash tonight. Presently, its about 9.40pm and I have had to fight with myself to wake up to go for a wee, that was about 9.00-ish. I even left work just after 4pm, I couldn’t even manage that last half hour, I had had it! I came home, had a snack of cheese and crackers and promptly crashed out in front of the TV bout 5.30...woke up enough to drag myself up to bed, quickly throwing my jimmie jams on and jumping into bed. Had a quick game on the iPad and promptly crashed out again! Thse blimmin eyeballs would not cooperate and stay open. They definitely had a mind of their own...I am now sitting up in bed with the wee fan blowing on me...hubby and big girl gone up the road to get some KFC for dinner.

Its heading towards the last week of work before Christmas. I was set to have a bery busy weekend this weekend but have had to put off my Sunday plans to ensure I get some much needed down time before work on Monday. I am gutted as so desperately wanted to catch up with this friend but have recognised that my body is calling out ‘enough!’

I need to desperately make sure I go to sleep early this week. Hubby and I have invited everyone from our office to come home after work on Friday for a ‘few’ drinks, order in some pizzas and have nibbles. I know for a fact it won’t be for just a few hours, so I need to make sure I am on my game - not for any other reason than for me to enjoy being with these people and having them here at home...a completely different setting. I am looking forward to it but have to say I was getting worried, knowing I had a full weekend in front of me, having been out this week, and having late nights, I was starting to freak out a bit.

This last weekend was chocka full. My sister flew over from Melbourne for the weekend. She was surprising a friend at a birthday celebrationon the Saturday. What a bloody awesome weekend it was too...sissy and I starting off having a quiet, civilised drink, catching up but the drunker we got, the sillier we got and ended up singing at the top of our voices, to the point where my baby girl apparently wanted to call noise control on her mother...๐Ÿ˜ ‘oops’ I don’t really drink very often either these days but it was so much fun. We all went our separate ways on Saturday. Hubby to a darts prizegiving and got home more pickled than a pickled onion, sister to her mates birthday celebration and the rest of us to a 21st. Sunday was a family bar-b-q so sissy could catch up with a few people before leaving home at the crack of dawn Monday morning. I got up just after 4am to say goodbye and so as you can imagine, everything including the tiredness has snowballed. Work Christmas dinner Tuesday night, yet another late night, my lovely cousin from Opotiki arrived on our doorstep Thursday night armed with some amazing Christmas goodies - it was just so lovely to see him and so grateful for the yummies. And then today, we had a shared lunch at work - it was pretty damn amazing...everyone completely outdid themselves so that seemed to top off such a crazy, busy time.

Unbelievable to think Christmas is only a week away...I am being very selfish this year. I think I spoke earlier about how this Christmas was about me and so I have done that. We are off to the beach for the day dependent on weather...will have very simple foods to take with us and have a chilled out day. The really funny thing is that my daughters boyfriends family are doing the same thing...at the same beach...I cracked up when I heard...I find that so weirdly funny but it will work out perfectly for my baby girl and her boyfriend, to have us all at the same place.

I am off work for a couple of weeks at the end of January / beginning of February and have booked myself a flight to Melbourne for four nights to stay with my other sister and her good friend she lives with, who I regard as very much like a sister. I am so excited about going to spend some time with them. We caught up when I was there earlier this year and E had said to me she would have loved for me to go stay with them for a couple of nights. But logistics between where both sisters live was too complicated. So my brain has been ticking over since I got home on how to do this. I am so, so looking forward to spending some time with them both. Its only a short stay but it allows me to have some chill out time and do stuff here in NZ before I go back to work.

Come January, it will be two years since I was diagnosed metastatic. Two years...In some ways its hard to believe, in some ways it feels like it has gone quick but the part that scares me a little is that, it is two years of my life that has gone, leaving me with how many more? I don’t know...by that I mean, while having this cancer I may live for ten years with it, two of those years have gone already...that leaves me with only another 8 to go. Its a scary thought. And yes I know none of us know when our time is up. But believe me there is a distinct difference between living your life and then you die, compared to having it hanging over your head knowing its going to come, but you don’t know when or how bad its going to get before you do. It can truly headfuck you but the trick is to try not to let it, or not to let it too often. The comment I so often get is “well we’re all going to die one day”...that comment just completely pisses me off. I try to be polite and smile but honestly as time goes by, I am getting less and less tolerant and say what I think, to a degree. Kind of depends on my mood...I can’t stress enough how different it is when you know you have this disease in your body that will one day kill you, even if that day is years away. Before cancer I would sometimes think about dying and actually I would wonder what would get me in the end (never for a moment think it would be breast cancer) but it was always a passing thought but knowing of course it would happen one day. Having cancer makes it a whole different ball game. It is on my mind often, it has become very much my reality. I don’t even know if this makes sense. To me it does. But you know, while knowing this disease will get me in the end one day, it is how it affects my life on a daily basis that I really dispise. Yes I am well and I am so very grateful for that...long may it continue. But its the simple things like the weariness I feel, having to be aware that I need to get plenty of rest, don’t over-do things, (or I end up crashing like tonight) leaning over into a cupboard makes my back ache, the constant aching and now with summer here, the throbbing feet once again...these things combined on a daily basis can be such a drag...but hey, it could be much much worse. So I try not to complain too much and take it on the chin. But there is a definite difference in ‘before cancer’ and ‘after cancer’.

Friday 15th December 2017 - 11.49pm

Thursday 30 November 2017

Rest day today

5.30am - alarm goes off
5.40am - still trying to haul ass out of bed - body feeling very tired and heavy
5.43am - have shower, dry off and put pj’s back on
6.00am - hop back into bed - wondering if I am able to push passed this
6.41am - playing games on iPad awaiting respectable time to advise supervisor

I often wake up feeling tired or achy or don’t feel like going to work (not just since cancer diagnosis!) but usually once I am up and in the shower those feelings dissapate and I am good to get on with the day.  But this morning I’m just not feeling it at all. I don’t feel unwell, I don’t feel tired like I haven’t had enough sleep (although I am sure I will nod off quite easily) - my body simply feels heavy and feels like it needs rest. The thought of having to sit up in an office chair for hours and function in a worklike capacity - don’t think I have it in me today. Sometimes I forget I should be limiting how much I do, just so I’m able to get through a full week of work.

This last weekend was busy, both days. In hindsight too busy but because I felt good, was able to cope with it at the time. But thats it isn’t it...it hits me a little later and then mixed in with a few late-ish nights (haven’t been able to go to sleep early this week)  it becomes too much for my body to handle and I hit a brick wall - albeit, an invisible one. I can’t even summon up any enthusiasm for a cup of tea - anyone who knows me well will know just how unusual that is.

With Christmas almost upon us, what are we? 24 days away...there is a lot going on. Lunches, dinners, parties, drinkies...I am exhausted just thinking about it. I have a busy weekend coming up, and I am tempted to put off going to Saturdays lunch. I’ll see how I feel tomorrow when I am back at work. A rest day today may be all I need. Its days like today I have had to learn to accept and not punish myself for needing them. Although sometimes I am inclined to forget (briefly) that I have cancer and while I am keeping really well, it has to manifest in some way. So knowing and accepting I need today as a rest day is huge. Made much much bigger by the fact I don’t feel guilty about it. HUGE strides for me...

Afternoon: what I do struggle with, is that due to circumstances, this is now part of my life and I have to think about it and I dispise it. Do you ever come to terms with it? And all that it entails? Maybe the phrase coming to terms isn’t correct...maybe I should say ‘acceptance’. I accept this is how I need to think - accept I need downtime at various times because my body is working hard to keep itself well and so I need to do my bit to help. Don’t stop living life but allow some time to rejuvenate. I don’t know that acceptance is the right term either. What I do know is that I hate having to do this...I hate that circumstances with my health means I have limitations. Combined with being older, carrying too much weight...is it even the cancer that does this to me? Or is it simply a convenient excuse to use? In all honesty, I don’t really know. I do know though that the levels of tiredness have definitely increased. They can be completely overwhelming and I definitely struggle at times to cope. At those times I wonder if this is how an elderly lady in her 80’s or 90’s must feel. While my girls think I am an old lady, I’m still relatively young. Early 50’s is not old yet I feel it. I feel old and frumpy...

I’m glad I have taken this day for myself. I watched some recorded programs on TV earlier this morning but have spent the majorityof the day lying down in bed. Had a wee sleep, not too long but enough to take the edge off. I will be ready to face the world again tomorrow. Oops eyes are starting to feel droopy again. Might squeeze in another nap before its time to get up and cook dinner although its still early.

Thursday 30th November 2017 - 2.41pm


Tuesday 21 November 2017

Memories flood back

I am sitting back in outpatients at Northshore Hospital waiting to see the plastic surgeon who operated on me putting in my implants after I had my mastectomy. Its a weird feeling being here after so long. I don’t even remember the last time I was here. Nothing has changed...its still the same funny little place with the same smell. The ‘short stay ward’ just sitting behind it. One of my many regular wards I stayed in. A nurse came out before to ask if I was waiting for a mammogram...if only, I thought to myself. But those few words have unleashed a lot of thoughts and feelings.



A mammogram...thats where this nightmare began. Why couldn’t I have been one of those women diagnosed (or preferrably with nothing to diagnose at all) but if I had to be diagnosed, why couldn’t it have been with a lump that could be cut out, have chemo (ugh), radiotheraphy and then just get on with my life. Not having to worry about what life expectancy I may or may not have. Wondering if those cancerous cells are swimming closer to my lungs or my liver, or my brain.  But it would probably have been my luck for it to have come back again anyhow. This is the path I was destined to go down. For what purpose I ask myself? To spread the word with my story so I can save someone else? While it would be wonderful to think I may have saved someones life by educating them with my journey, I will never ever know. But I can only hope my being so open does help raise awareness.

I haven’t missed this place...the endless visits back when I first had my surgery. Seeing both the plastic surgeon and the breast surgeon at different appointments but at the same funny little place. Being poked at, prodded, endless people looking at my implants / scars, having dressings changed and so on. It seems like such a lifetime ago but it wasn’t really.

My appointment:

Surprisingly I wasn’t examined. I thought with the length of time since last seen, they may have needed to. Mr K was quite astonished when I said it had been 16 to 18 months since I last saw him. In fact, it was June 2016, so I was pretty much on the nose. What he wantd to know was whether I wanted to have further surgery to replace the implant I lost, or would I be happy to have my case signed off. I told him of my concerns about my dislike for both my implant and prosthesis, was I brave enough to have the implant removed and stay flat, finally ending with how I feel these days I have bigger and better things to worry about. Mr K agreed with me. He said there was always the concern that having surgery may compromise my existing cancer condition and reminding me of the old saying ‘if it ain’t broke, why fix it’. He asked if I would like a further six months or so to think on it more and I said no, lets sign my case off now. And so we have...Feeling a tinge of sadness. This man was a big part of the beginning of my journey with breast cancer. While someone else removed my old breasts, Mr K gave me new ones. He tried to save my infected one, deciding in the end it was better to remove it. My endless appointments with him, that have now come to an end. We shook hands and he wished me luck and expressed his sorrow at how things hadn’t turned out the way we would have wished and I had to fight back the tears. Coming home and relaying it to my husband, those tears finally fall and then again as I type this.

Another appointment next month to see the breast surgeon, back at the same place. I wonder if that visit will evoke old memories and stir up thoughts and feelings I would rather not have.

I lie on the bed, the sky is a beautiful blue and the sun is streaming. Summer is definitely making an impression. How can you have such sad thoughts and feelings on such a beautiful day. God, I wish circumstances were different...



So on this beautiful, sunny late afternoon, it looks like the decision has been made. I will continue to be lopsided, having two breasts when I feel like wearing my prosthesis. I now have to come to terms with having this implant which I don’t like, and get used to the ugly unsightly cavern where an implant briefly was before it became infected, eventually filling with poison. This is me...time to come to terms with it.

When I take my bra off, I am very conscious of the fact that I feel like a weight has literally been taken off my chest. The prosthesis can feel very heavy some days and I drop it on the bed with a sense of relief, feeling a bit like its a small bowling ball or bag of sand.I am then conscious of the fact that I have one breast sticking out of my chest wall. An un-natural one. An immovable object that just stays. No jiggling to be had. And then the opposite side to the immovable object, is this ugly bulk of puckered skin. It serves no purpose except as a reminder of what I have lost. Do I feel less of a woman because of it? No, definitely not. Do I feel embarrassed by it? No, I don’t think so...its just a part of me now. But its an ugly part which I don’t like. I try not to look at it. I know its there and as I put my bra on with the prosthesis inside it, it is yet another reminder of what I have lost.

I wish I could say all I have lost are my breasts but I have lost so much more than that...

Tuesday 21st November 2017 - 6.21pm


Saturday 18 November 2017

Anti-social undies

I have had the laziest, most chilled out Saturday and have loved every moment of it. Had a lie in this morning, then got up to watch my recorded programs. Then my big girl and I watched the last episode of ‘How to get away with Murder’ - one of my most absolute favourite programs. It has been a ritual each Saturday, followed by watching a couple of movies. I am now hibernating in my room with a fresh cuppa. Its been a relatively busy week. Treatment at the hospital on Monday, nothing out of the ordinary with it, out for dinner with friends Wednesday night, works AGM on Thursday night, and so hubby and my baby girl came with me and we had dinner before hand. Admittedly two nights out, even if they are early finishes (home by 8.30), I am exhausted. Tonight the boss was putting on a social occasion in town for everyone at work. As recognition for all the work put in by all with the new system having come into play. Thats where the name of this post came from. My boss asked if I was going to the AGM and I very emphatically said no, I had been going for years, it was time for the newer staff to do their bit. (We usually attend to ensure there are enough numbers and by living close by, we are the ones relied upon. The south Auckland crew get off due to the distance to travel, which never seem to be such an issue a number of years ago. But as time has gone on, traffic has gotten heavier and they just haven’t been expected to attend). But anyhow, I am steering off course. Anyhow, my boss said to me, I hear your not coming along on Saturday either, have you got your anti-social undies on? To which I said ‘yes I have!’ I told him I am not in the least bit interested in socialising outside of work and the weekends are my time. And I don’t regret that decision for one moment! I came home yesterday relieved in the knowledge that I do not have to have anything to do with work until Monday. If I socialise with workmates, it is my choice. However, I did have second thoughts about attending the AGM. I get a lot of support from my boss with regards to everything that has gone on, and he doesn’t ask much of me, apart from doing my job. Attending the AGM is one small thing I can do to show my support to them, even if I haven’t agreed with recent decisions - not that they are answerable to me, or have to make any kind of explanation. Hence going and having a good catch up with some I haven’t seen in a long while.  It was actually really quite nice.

Its been raining off and on most of today...on at the moment and it is so relaxing. Left overs from last night for dinner tonight, so no cooking having to be done...god, this is the life! One more day of the weekend to go, with no set plans.


Tuesday afternoon I have an appointment with my plastic surgeon. Its been possibly 16 months since I last saw him. He said last time “see you at Christmas time” but his nurse told me his Christmas time would probably be closer to March. Both came and went and almost a year later, I finally get one. Not that it worries me, all is well with my implant and non-boob side. If I was to say anything to him, it would possibly be, please take my other implant out. I don’t like it, I never have and I can’t see it happening now. I have days where it feels tight or heavy on my chest - much like the prosthesis. In fact, I just made the comment the other day to my workmates that my false boobs felt tight. The thought of having to go under the knife again does not appeal at all, or having to use my annual leave for recovery time. I’d much rather use it for recreational recovery.

Next month I have an appointment with my breast surgeon. It will have been 12 months since I last saw her. In all honesty, I have no idea why she needs to see me and must make a point of asking.

Come January 27th, it will be two years since diagnosed metastatic (stage 4, incurable, advanced, terminal). Wow...has it almost been that long? I’ve been going round ‘cancer headfucked’ that long? Not sure whether to be scared or impressed. Scared that two years of my life expectancy is now passed or impressed that I have come through it and still in reasonably good health and doing ‘ok’. Bit of both hangs in there...you can’t help it. You just try not to dwell on it too much. Think there is room for improvement!

Saturday 18th November 2017 - 8.03pm

Wednesday 15 November 2017

Deactivation complete...

I’ve done it! I deactivated my facebook page last night and I feel free!!!!! I had to download a game onto my phone so when I pick it up, I still have something to do on it. Its a bit like mind over matter. I could have kept the page but I would have kept checking it periodically and with the way I was feeling about it, it would completely aggravate me. I had gotten to the point where I loathed everything about it. So a break away will be great, even if only for a week. Who knows...

I don’t have anything else to post, simply felt the need to share about what I had done. I feel quite proud of myself, stupid really.

Its halfway through the week thank goodnesss. Been out for dinner tonight with my ‘young friends’ to a lovely little Italian restaurant local to home...absolutely delicious and look forward to going back another time to try something different. Now lying on the bed with a full puku, time for a cuppa soon maybe (or not). Two more days of work before the next weekend. Time is really starting to get away now withChristmas closing on in. I have applied for a couple of weeks leave towards the end of January. Hopefully the weather will be great to do some day trips away. Another year almost gone..where do they go?

Wednesday 15th November 2017 - 8.28pm

Sunday 12 November 2017

Facebook friends

I’ve been culling my ‘facebook friends’. What a stupid term...what even are they? A bunch of people who send you a request because they want as many ‘friends’ as possible or they met you briefly through someone and think it gives them the right to see into your life and check out your photos. And you know what, we’re daft enough to accept it. I know I am...I accept requests because I feel awkward not accepting them (not all the time, but some) and I allow people the passageway into a glimpse of my life. Well I’ve kind of had enough and so I started culling them. Both friends and family who I no longer hear from or never ever really heard from. Why should I give them a glimpse into my life? While I cerrainly don’t hold back on anything to do with my breast cancer, and I try not to post too much on fb, sometimes I do. Why should they be freely given access to it? Its different with this blog...While I know I have a few regular readers, I don’t really know otherwise who reads this, if anyone. I get stats from blogspot but in all honesty, I can’t make head nor tail of them. And thats all ok...I was geared up for the possibility of people I don’t know, reading this and of course part of my reasoning was to help others in the same boat, maybe my thoughts would be their thoughts, I don’t know...and the other reason of course was for family and friends to know firsthamd whats been going on whether with oncology appointments or inside my head.

But I just figure that if people want to know what’s going on, they can bloody well make contact and ask. And yes even after talking about this ages ago, it still hurts that some people I would have expected more from, don’t bother with me. I try not to let it, but those feelings continue to slip in. Funnily enough, when someone dies, we all make the time to attend the funeral but how about making the time while they are still alive and can enjoy the benefit of your company? We’re all guilty of it...I know I am. But I am now on the flip side where this is happening to me personally. I kind of figure if you can’t be bothered making time for me when I’m alive, why bother when I’m dead...except hubby and girls may appreciate you being around then. Unless my bitterness rubs off onto them and they are as offended by the hypocracy as I am.

So yes, a start has been made and I will hopefully continue with it soon before I lose the momentum and stop giving a shit until the next time. I am having trouble keeping my eyes open, so will stop off for a girly break and come back to bed and crash out. I hate to think how many spelling mistakes I will have missed. I try and check them regularly as I type but I find using the ipad, my fingers regularly hit the letter next to the one I actually want. ‘N’ and ‘m’ is a classic one...usually missing those when I spellcheck with my blind, tired eyes!

Anyhow, thats me...

Sunday 12th November 2017 - 2.27am


Monday 6 November 2017

Countdown to Christmas

49 days until Christmas...whoa...

I love Christmas! Over the years I have enjoyed the big family Christmasses, and enjoyed the quiet ones with just us. Last year in all honesty felt like a non-event. The boys put a small umu down at their mums place and then proceeded to get plastered. I played board games with the kids (big kids) and it didn’t feel in the least bit like Christmas Day but think it had more to do with my state of mind. It probably didn’t help that I had one foot in a moonboot after falling through a chair and breaking two toes and suffering from horrendous pain in my tailbone, and worrying about the possible implications this could have with the cancer being in my bones. Especially already being in my lower back extremities.

This year I would like a chilled out day, preferrably at fhe beach but the weather is always so unpredictable. I don’t want lots of food with all the trimmings - I would like a no fuss day that is enjoyable. If we go to the beach, we can swim, lie in the sun, play board games and hubby and kids can have a few drinks. I am more than happy to be the driver. For years I have wanted to do this but worried about the trimmings. How would we keep the pavlova fresh? How will we keep the ice cream frozen? This year I have a little more clarity. Its more about having an enjoyable day with my wee family. The food is simply fuel to keep you going. What it is, is not important. Hubby has never liked this idea but I think I’ll push for it...it can be on my bucket list. Its probably the one thing I can truly think of that I want to do.



My big girl and I went out Friday night. I’ve had a bit of a bee in my bonnet about doing some Christmas shopping, and had made a start a couple of weeks ago. The reality was that once we got to the mall and after looking in a couple of shops, the exhaustion of the week caught up with me very quickly and the enthusiasm waned comsiderably. But we decided we’d try again the next morning and go to St Lukes instead. Which we did and it was bloody awesome! I was so pleased, I got a lot out of the way and my big girl was very pleased with her purchases as well. It feels great, just wish our Christmas tree was up so we could wrap the pressies and pop them underneath!



This year I am being featured in a Christmas edition newsletter for BCFNZ. Its designed to raise donations for their continued support of women with breast cancer as well as to raise awareness and fund ongoing research. The newsletter will be distributed to approximately 75,000 people and will also be utilised through social media.

Hard to believe it’s only been a week since I was feeling so crap. I thought it was never going to end and it’s bloody wonderful to feel reasonably normal again. Still a few ongoing issues such as endless headaches, had a bout of tummy and bowel issues but think they are slowly resolving. Either way, I am feeling so much better - thank goodness! I had been worried about going back to work, thinking I had probably forgotten most of what I has learnt with the new systems which had recently come in and yes I had...but it was a matter of sitting with someone to refresh my brain or sitting down and nutting it out for myself. I think I can now say I’m feeling quite a bit more confident. Wish I didn’t doubt myself so much but I do it all the time. I want to know everything instantly and get pissed off with myself when I get confused. A huge part of it is my memory. I know my memory is shocking these days and it instantly worries me and puts me on high alert. And I am immediately in turmoil before I have even started! So I have pleasantly surprised myself...with a huge sigh of relief!

Five and a half hours before my alarm goes off and a new week of work begins. I had a 2.5 hour sleep this afternoon...I was bloody knackered and could hardly keep my eyes open...now I’m having trouble going to sleep but to be honest haven’t really given it a try. Tummy is starting to rumble naturally since the subject of going to sleep has arisen..what a bloody nuisance.

Wonder what this week is going to bring...normality is always good:)

Monday 6th November 2017 - 12.29am




Sunday 29 October 2017

And so the misery continues

Night 6 since this fiasco of a bug began. While the razorblades and pounding headaches have ceased, the scratchy throat has taken over, with damn awful hacking and coughing occurring all night almost to the point of vomiting. This god awful gel shit the doctor ordered to numb my throat is a joke. Its a thick gellified goo which ‘plops’ into a glass and the same thing happens when you try to use it for your throat. Its a mission even getting it anywhere near the base of your throat which is where the scratchiness eminates from. Given up on it (gel I mean).

Its been six nights of pure frustration and bugger all sleep. I had really been hoping once the razorblades and headaches left, I would be able to finally get some sleep, but no...last night I was up and down from the lounge to the bedroom, trying to decide where to sleep, worrying I would wake hubby up with my endless hacking. But was so uncomfortable in the lounge, trying to sleep sitting partly upright and the comfort of my bed was calling. So gutted...was so ready for a decent nights sleep finally, but no, it isn’t meant to be. Not yet...

Its a little before 4.00am Sunday morning. I’ve been awake since about 3.00 hoping I’ll quickly nod off again. Tonight has been the best sleep by far. My older daughter and I were watching a netflix series and partly into the third one, I nodded off and got a hell of a shock when she woke me up at the end of it and told me I had slept through most of it. Awesome! Never been so happy to miss a programme in all my life. Waddled off to bed with a lozenge to help ease the not too bad scratchiness and happy to report I was able to go back off the sleep - that was about 11pm. Scratchiness has well and truly settled back in now, so propped upright, had a lozenge, some ibuprofen and paracetamol, a cup of warm water beside me to sip away on - hoping this combination will ease it.

Sleep...somehing we can take for granted. I worry a bit when I don’t get a decent amount of sleep (which is too often) when I have work the next day, but am able to wing it by having a nap when I get home after work. Its not ideal but I can make it through a week of work, wishing everyday was Friday and finally by that lovely blessed day, I can hardly wait for 4.30pm to come when I can jump in my car and go home for two whole days. But THIS! This has been something completely different. Hardly any sleep each night and knowing everyone else in your household is fast asleep and your worried you might wake them with your wanderings around. Thursday night, Friday morning I was so distressed, I ended up ringing the emergemcy number. I was absolutely beside myself. My head felt like it was going to explode, my ears were blocked and sore, made worse by using the waxsol the doctor had prescribed, not so much the razors although still there. But I just didn’t know what to do, and I knew I didn’t have anything in me to go up to A&E so I rang emergency. The dispatcher got someone to ring me and although after asking lots of questions, were able to give me some advice  which I followed. Instead of taking the painkillers I use for my cancer aches and pains, I should have been taking ibuprofen. Within half an hour, I could feel the relief kicking in. I felt a bit stupid to be honest, but these days I am so forgetful and it never occurred to me to take those. Funnily enough they’re keeping my aches and pains at bay as well. I womder if I should continue taking them instead of the other stuff...

Today I have felt like a wrung out dishcloth, or how I would imagine one feeling if it could feel. Eyeballs hanging out but just haven’t been able to nod off. Finally crashed out on the couch late afternoon for a little while, but really need to try and catch up on some sleep later today. I am aiming to go back to work tomorrow, but in all honesty, I don’t feel I can or should. I don’t know that my body is ready to go back into that mode of waking up early (if I’ve even been asleep) and having to sit up for eight hours in an office chair. I don’t know, lets see what the rest of today brings. Even the doctor said to me that rest and fluids are the main things required to get better.

So on that note, lets hope that this is the last post about this damn virus, givng you every single account of what is going on. But in all honesty, it gives me something to do during these dark, quiet hours and it brings a sense of relief being able to get it off my chest. Cancer has definitely taken a back seat this last week and I have to admit I really like that! So many people have made contact and said they are always there is I need to be taken anywhere, no matter what time of the day or night. Their offers are so appreciatd but I am not the sort of person who does something like that easily. I have never found it easy asking for help and that continues now. I would imagine, depending on how urgent it is, would absolutely depend on whether I call someone for help. I had to do it in the early days of my diagnosis, especially all those horrendous trips to the A&E when I was having problems with my wound infections.

The scratchiness seems to have eased now and I am slipping down my propped up pillows, feeling quite uncomfortable. Hopefully I can nod back off to sleep again...think I’ll give it a try.

Sunday 29th October 2017 - 4.40am


Friday 27 October 2017

I am a terrible patient

I am going to drive you crazy...I am going to drive myself crazy...

I hate feeling like this! I feel almost ridiculous even saying this, but honestly right about now, I feel being struck down by this stupid whatever it is, headcold, virus - whatever, is worse than having bloody cancer. I don’t mean to be flippant, or maybe I do. But since having cancer, I have not exhibited any kinds of symptoms that feature so prominently and in your face.  Not even when I had my boobs cut off...I don’t remember feeling this bloody miserable. Maybe I was and I’ve simply forgotten.

I get a bit of a reprieve from  mainly the pain in my throat but the headaches have been fairly constant. They lessen for a while but don’t allow me the luxury of completing disappearing even for a short while. My head is starting to pound at full volume and the sore throat is coming back. I have filled both ears with waxsol ear drops and shoved bits of cotton balls in to block the stuff in. I have given up on the paracodeine and gone straight for the big stuff. 2 x 30mg codeine tablets. I hope they kick in soon. I am almost beside myself, I just don’t know what to do.

Drink lots of water the doctor said, the headaches are from your high temperature. I feel like I have drunk enough water to sink a battleship and my wee’s are almost clear! How much more do I need to drink and why won’t this stupid headache go away????

When hubby went down the road to pick up my script, he was given everything but the shit to gargle and numb my throat! The stuff I needed the most...I am terrified at the thought of having another night like last night hence taking the stronger painkillers. The chemist people were going to order the stuff in and it will arrive tomorrow morning. The doctor said to me if I feel like I am getting worse to start taking the antibiotics she prescribed just in case it is bacterial and not viral. Does this constitute as getting worse because its not getting any better? Or am I just being a terrible patient and being irrational and impatient?

Funny eh, that something as simple as a sore throat and a few headaches can cause me so much distress. When I stop and remind myself I have cancer in my body...cancer that has escaped through my lymph node system and buried itself into some of my bones. This is probably one of the very few times where the cancer has taken a back seat, almost completely forgotten about, and it feels great! I feel like a normal functioning person, like I used to be almost two years ago.

Two years...shit I’ve just realised it is exactly two years since I was diagnosed with breast cancer. It seems such a long time ago and so much has gone on during that period of time. The shock of being diagnosed, not just in one breast but in both. The reality of waking up after my five or six hour surgery realising my breasts which nourishd my babies have gone and implants have taken their place, and not just that, they are also smaller - at my request! Come January, it will be two years since I was told I am metastatic. Two years of my advanced breast cancer years gone...leaving me with how many more? I want time to slow down...its going too fast. It doesn’t help when I am constantly wishing it was Friday so I can have the weekend to sit and do nothing if I so wish. I remember one of the ladies at work many years ago saying to me ‘stop wishing your life away Tania’. I always used to laugh at her but also realising the truth in what she had said. But now of course, it has an even truer ring to it. My life...my shortened life because of this stupid disease.

Even if I was to survive ten years, I have had almost two of those years, leaving me with another 8. While thats quite a reasonable amount of time to live with advanced cancer, it still isn’t very long. When you don’t have this diagnosis, you still don’t know how long you will live but you have the luxury of being able to dream you will live until you are in your 80’s and to see geandchildren and possibly great grandchildren. I don’t have that luxury, not if I am being realistic. Thats not to say it won’t happen. I would love to surprise myself but I really dislike it when people say to me ‘of course your going to live for years and years’. How do they know that? Are they privvy to information that I’m not? I need to be present in the real world with no false ideals. This is my way of coping with it. And if its too hard for someone to hear it, well too bad. This is my story, my journey - I am the one who has to deal with the facts and I don’t appreciate it when what I am saying or that my feelings are being dismissed. You think you find it hard dealing with the reality of my diagnosis? Take a moment and imagine what it is like for me. Knowing I will leave my husband, my beautiful babies. God, that is what tears me up inside - rips my heart into shreds. Knowing from the day I leave this world, I will never see my beautiful daughters again and knowing they will be shrouded with grief and I won’t be here to help them. These girls whom I gave life to, these girls who already lost their father at such a young age...these girls whom I love and adore more than anyone else in the world, the reason I was put on this earth...one thing is for sure, we will all die one day, but a diagnosis of a terminal disease regardless of what it is, hangs over you from the day you are diagnosed to the day you die. What a waste of energy.

Well that put a spanner in the works didn’t it. I was going on about how my throat and head had made me completely forget about the cancer and it comes back with a bang! Neither of those things have settled down either. Still got the blasted headache and my throat is getting a little more sore. What time did I take those bloody tablets? I know they take quite a while to kick in and you are only supposed to take them every 6 hours. By the time the damn things kick in, you really only get a short reprieve.

I hope this virus or whatever it is, gets on its bike very soon. I am hating feeling like this...

It is supposed to be pink Friday at work tomorrow and I was going to go dressed up in my pink breast cancer tee-shirt, fairy wings and tiara which I wore when I did the Pink Ribbon Street Appeal. I am disappointed I won’t be able to participate but guess getting some rest and recuperation time is more important.

Friday 27th October 2017 - 12.06am

Thursday 26 October 2017

Doctors visit for razorblade throat

Thank goodness I finally got to my doctors appointment this morning. I put a message up on facebook saying how I wish someone could take me as I was feeling dizzy, nauseous and was worried about driving as I had also only had minimal sleep throughout the night. I had a number of offers from people, and cripes how humbling. Anyone who knows me well will know I don’t ask for help very often and actually I didn’t really expect such a response. I don’t know what I expected...I just put the post up without thinking. My lovely sister-in-law came and picked me up, so it was a great chance to have a bit of a catch up. I am now home and tucked up in bed. So a huge thank you to my sissy-in-law and also to everyone else for their thoughts and offers. I am so lucky to have so many willing to jump in and help.

My appointment: The doctor gave me a thorough going over - she is just lovely. I have pharyngitis which actually is just a flash word for sore throat. My glands are really sore and at first she thought it was probably viral but soon discovered I have a high temp (37.9 - not that high if you ask me) so has given me a script for antibiotics just in case I get any worse. She thought with plenty of rest and fluids (water, not cups of tea), I should come right in the next few days. So I am home from work again tomorrow and also have the weekend to recover. Guess I should have listened more closely to my daughter and supervisor after all! The headaches are from the high temperature, hence why I need to drink more water. The dizziness comes from my blocked ear and has nothing to do with the throat or cold. It is purely packed solid with ear wax (how embarrassing) and so she was unable to irrigate it. So I have been given some stuff to put in my ears (yes, both!) at night time for a few nights and then go back in a couple of weeks time so they can then irrigate them - damn, damn and blast! I didn’t really want to have to go back.

The doctor also gave me a bit of a lecture about my fatty liver results. I need to lose some weight and do exercise before the damage is irreversible. It was quite good, she explained the importance of why I need to. So maybe, just maybe this will get me in the right mode. Also the paracodeine which I swallow on a very regular basis is not conducive to my liver and she is going to try and wean me off it and use something else. She wants me to take something called nortriptyline, at night before I go to bed. Details get a bit hazy here...this stuff will re-route from my brain or to my brain, how I feel about the aches and pains I suffer from, and to stretch out the time between doses of paracodeine. From 4 hourly to 6 and then eventually to every 8 hours. I don’t think this will be too much of an issue as sometimes I do that anyhow, without meaning to. I just forget to take it. I worry about taking new medication without the say so of the oncologist as I think my cancer meds take precedence over everything else. When I mentioned this to the doctor, she was great and said they have this app or something where they can check if any new meds can affect your other meds. This came up as good to go...but I still feel a little nervous. I might ring the oncology nurse and pass it by her to check out with one of the oncology doctors. Simply for peace of mind.

Hubby has gone for a walk down the road to get my script filled out. I might go and have some lunch and have a snooze. I have had bugger all sleep throughout the night and my eyes are feeling a little heavy. Think this tired body requires some much needed rest.

Thank you again everyone for your thoughts and concern. For the early morning phone call from an old friend who was concerned when she read my early morning post about my pounding headache - was lovely to catch up and look forward to seeing you in person very soon - for the offers to take me to my appointment - for the offer from my Opotiki whanau to pay for an Uber - for the concern shown by my supervisor - my cousin in Howick who wished she could come and pick me up - my daughter who would have taken time off work to take me -  to Shell for picking me up and dropping home again - to everyone! You are all amazing and I am so grateful to, and for all of you.

Thursday 26th October 2017 - 1.26pm





Razorblades in my throat

Its 2.13am Thursday morning. I don’t quite know what exactly woke me up, the need to go for a wee probably but coming to the realisation that I am in absolute agony. My head is pounding, my throat feels like it has razor blades in it, my jaw is aching and feels tense and my right ear is blocked yet has this muffled ‘boom, boom, boom’ eminating inside of it and I absolutely have no idea what to do with myself...I drag myself out of bed, and manage to take some painkillers though wondering how long before they will kick in. Then I just lie in bed and wait...thinking to myself if someone was to ask how high is the pain? I could easily say it is a 10/10. That was maybe an hour or so ago now. I am relieved ro say the painkillers have kicked in and while my head still pounds and my throat is still sore, the effects have lessened, thank goodness...

I started feeling like this on Monday - labour day after I woke up from a sleep late afternoon. I woke with a pounding headache and the beginnings of a sore throat, which escalated as the evening wore on, by about 8.00pm, the razor blades had pretty much made their presence felt. I took some painkillers quite determined that a sore throat was not going to prevent me from going to work the next day. Especially if I could keep on top of the pain and so I did..both those things. Went to work, took painkillers every four hours on the dot but by 3.00pm I started to feel crappy, with a twist of head spinning and thought bugger this, I am going home before it either gets worse or I have to drive like this in peak hour traffic.

It always seems to be as evening hits or early morning when your symptoms kick into overdrive. Tuesday night those damn razor blades made their presence known. Unfortunately the painkillers decided not to work so it was a damn uncomfortable night, trying not to swallow too much, drinking warm water, gargling with water and salt but managing to go to sleep, woke up early Wednesday with the same symptoms deciding a visit to the doctor was needed. If my throat is that sore, there must be a reason and it needs to be checked out. So after the usual inner struggle with myself I decided to stay home and at 8.30am (opening time), I rang the doctors to make an appointment and would you believe at the start of opening hours, they had nothing available for that whole day!!!! Was it urgent she said? Is an extremely sore throat and constant pounding headaches in someone who has terminal cancer urgent? I didn’t really think so...but I was not happy. She said she would ring me if any cancellations came up. I got no phone call, so I presume no cancellations or she said that to everyone, or else everyone said their symptoms were urgent and they HAD to have an appointment. As the day progresses to about midday, I start to feel much better and then the guilt starts to kick in. OMG, I could have gone to work after all, I could sit at my desk working like this...but within a couple of hours, I started to feel crap again, quite thankful I hadn’t gone to work after all. It happens every time without fail - I always get a case of the guilts. I have always been like this, I have often said this, even when the girls were little and I had to stay home with them because they were unwell, I would feel guilty. I always felt torn between my family and work. Of course your family comes first, but part of providing for your family is having a stable job where you are able to pay the bills and buy food etc. Work has always been good to me and so one of the ways I could give back, was by being a good employee who doesn’t take the mickey. I still have that mentality now and even with having a terminal illness, feel guilty when I am away, which lately seems to have been a lot. My fear is that because I am away more than usual, they will think I am more trouble than I am worth and decide to get rid of me.

I was having an inner turmoil with myself this afternoon, wondering if I should go to work in the morning before I go to the doctors at 10.30 and see what the doc says as to whether I go back afterwards. My younger daughter is telling me to stay home and rest, but I am wondering do I really need to? My supervisor at work is telling me to put my health first and to listen to my daughter...and I know they are both right, its just me and the way I am.

But as I sit up awake at this early hour of the morning and with being so distressed a little earlier, I know something definitely is not right and so my body needs some down time to recuperate. Bloody terrible timimg though. New systems at work which I am still learning and I feel like this puts me back quite a bit, and actually I feel like I was doing pretty ok picking things up. But its the retaining of the information I am worried about. The more you do them, the more confident you become.

But my younger daughter says this is how she felt last week and was home in bed for quite a number of days. She didn’t go to the doctors but sore throats always make me a little nervous. When the girls were little, I was always worried they could have strep throat which could then lead to rheumatic fever and then my baby had two bouts of glandular fever at ages 7 and again at 13. One of the initial symptoms of it was the extreme sore throat and I remember the nightmare of a time she had both times. The fatigue especially, not just for a few months, but up to a year. My poor girl, every time she says she has a sore throat now, I inwardly panic. So with this bloody, not just sore throat, but bloody sore throat, I would feel a whole lot better getting it checked out. Not to mention get a medical certificate for work. Its a short week thankfully...

I wonder though, does having this terminal diagnosis complicate things? I wouldn’t really think so but the worry is there. Maybe its just a case of  like the other two said today, with my health concerns I need to be careful. What was it I used to say? “Be kind to myself - be kind to my body”

Its been a couple of hours since I first woke up and took something, the headache is still there, throat still a little sore (though a million times better thank goodness) and the muffled noise in my blocked ear is still ‘booming’ away and feels like phlegm is pouring down the back of my throat - ugh!

Roll on 10.30, I just want to go doctors and find out what is going on and put my mind at rest. Its  quite lonely being awake at this time. No one else awake to talk to, or to at least hear anyone else talking amongst themselves. Even the cats are fast asleep.

Cripes, I’d love a lolly or something sweet right about now...and then back off to sleep for a few hours would be great. Actually getting rid of this damn headache would be quite good too.

Thursday 27th October 2017 - 3.33am

Monday 23 October 2017

Lightness comes with a long weekend

God, how much lighter I feel knowing I have a third day to my weekend still to come! Usually on a Sunday night I am kicking myself because the next day is Monday and another week of work starts. Dragging myself around the house getting my lunch ready, picking clothes out to wear the next day, fighting with myself because I know I need to go to bed early yet not wanting to. But tonight, I feel so relaxed just knowing I can sleep in again tomorrow morning and have another whole day to myself. This doesn’t particularly help me in my mission to talk myself into how good it is to stick it out fulltime at work. Imagine feeling like this every Sunday...knowing you have that third day to chill out. Aahhhh.......Oh well, dreams are free and guess I’ll just have to make the most of these long weekends as they come round.



Its been a lovely few days, participated in Diwali celebrations Thursday night, had lunch with my big girl yesterday after we potted round getting a few things done of which one was buying myself a new mobile phone. I’m so excited and goddam I bloody love it! What took me so long getting one???? I know, the guilt of spending so much money on something so small and what I felt was frivolous and un-necessary. But actually when I really think about it, I don’t think it either of those things. And I figure, goddam I work hard, I drag myself off to work fulltime even though I’m not the best of health, keep the household going financially and I just figured “fuck it, I deserve it!’ and mobiles are such a big part of our lives now. It’s a means of contact with others when using landlines isn’t an option. Actually if it wasn’t for hubby’s mum, I might even have contemplated cutting the landline off and just using the mobile.

Today I was able to catch up with a friend whom I have not seen for so long and I wonder what tomorrow will bring. I have a bit of a bee in my bonnet at the moment about getting a start on my Christmas shopping so who knows. I might go off tomorrow and get a start on that. Either way, its my day off and I can spend it however I choose.

I had been invited to a couple of birthday celebrations for Saturday night. I had said no to both of them. On one hand I was recently moaning about having no social life in the weekend evenings and then I get two invites for the same evening and say no to both of them. I have my reasons why I didn’t attend either of them and don’t feel I need to go into any detail to explain myself. I don’t say no for the hell of it or to be spiteful or rude, I usually just don’t have it in me to go. I would assume that people who know I have breast cancer will understand without any long winded explanations. But in actuality, one of these celebrations I would very much liked to have gone to except it was out of town and so for a number of reasons felt I wasn’t able to go.

It has taken me to get cancer to realise I don’t have to offer an explanation of any kind. I have days where I just don’t feel like doing stuff and so I won’t. I try not to muck people around. If I say I will go somewhere, I try very hard to stick to that decision but there are times when I just don’t feel up to it. I think because I ‘look well’, people assume I am and so expect me to go on with life as normal. But there are days when I just am unable to do that or just don’t want to. We have a social event coming up at work soon - I won’t be attending. In this instance, I simply don’t want to. My weekends are precious and they go so quickly as it is. Work already has me for 40 hours each week, that is enough. Do I feel guilty? Not in the slightest. I’m over doing things because I feel obliged although that still kicks in every now and then but it is getting less. Maybe I do have an attitude problem, a sense of entitlement because I have the dreaded ‘cancer’. My attitude has definitely changed, not necessarily for the better either. At least I acknowledge my faults. I’m just not sure I care enough to change them.

Monday 23rd October 2017 - 12.11am








Monday 16 October 2017

Waiting room, Oncology - building 8 - 16/10/17

My thoughts as I wait my turn:

I hate this room - this waiting room full of people who have cancer and their loved ones. Most people have someone with them - I am alone. But it doesn’t worry me. It’s only when I’ve had scans and waiting to receive results that I feel I need someone with me - in case you get that awful and devastating news, that the cancer has shifted further afield.

There’s something terribly depressing about this room. We’re all waiting, the doctors come to call out a name and you look at them expectantly wondering if it will be your name they call. You look at the other people here and wonder what sort of cancer they have. Some look well like myself, others have headwear on and so you know they have had or are having ongoing chemo. Having poison poured through their veins in the hope that it will kill off the cancer or at least send it into submission for eternity (I don’t really know what chemo does).

I still think this appointment is a mistake. I should only be here for my treatment and then be on my way to work. Guess I’ll find out soon enough. Briefly the thought goes through my mind, did they forget something at last months appointment? Did they see something in last months blood tests?

I can hear the people around me chatting. I don’t want to catch anyone’s eye - I don’t feel like smiling at anyone - I don’t feel like talking or being sociable. I feel like today is not such a great day in my head. I feel like the positivity has seeped out and completely left me void. I am an empty cancerous shell. I have the realisation I am MBC - with no cure. I mean of course I have known it all this time and most of the time I just get on with it. But sometimes it smacks me in the face all over again. I wish I could just get on with life and enjoy it but the constant aches and tiredness are a never ending reminder and so instead of enjoying time, you spend it hating cancer, feeling anxious, hating the ongoing symptoms you exhibit and its bloody exhausting to be honest.

Treatment time:

Oncology appointment over, now down at acute oncology for treatment. No sinister reason for the call back this month - she just wanted to check something out. We had stopped some tablets I was taking, not cancer related and just making sure no issues arising from it.

My calcium levels are elevated which could be due to being dehydrated at the time of the bloodtests. These are being checked again today and so the nurse has taken them but is reluctant to start the zometa infusion until she finds out from the oncologist if we need to wait on blood results to see if I need a drip to help hydrate me before the infusion.

While I wait for the nurse, I can see a tow truck is hooking a car up and the hospital clerk has just come in to make sure we all have our oncology paperwork on our dashboards. Getting stricter and who can blame them...these carparks are for the convenience of those of us who need them. Its like disabled carparks - they are there for a reason and shouldn’t be abused.

Nurse has come back - oncologist just wants to see trend of calcium levels as they have been on the rise for the last three months . No waiting around required - hook up of zometa infusion starting and I’ll be out of here soon.

This little unit ‘acute oncology’ is so much nicer than building 8. Maybe because it is smaller,  not so many people. I just find ‘8’ so depressing. Perhaps its simply because of what it stands for...

*********************************************************************************

These were my scribblings in my notebook today while I was waiting to be seen and during treatment.
I won’t see the oncologist for another three months, so January 2018. They will send me for a CT scan before so I can get results at the same time. These are the results that make me nervous - they show if the cancer has spread. Its a constant fear that is always in the back of your mind...but for now I will continue on the same regime since it’s working well

Monday 16th October 2017

Sunday 15 October 2017

Giving back day


I was a volunteer for the pink ribbon street appeal today for a couple of hours. I had my ‘knowledge beats breast cancer’ tee-shirt on along with some pretty pink fairy wings and a pink fluffy tiara. It felt good to have a bit of fun while doing something so important for such a serious issue. This is my own personal feelings, not everyone feels the same way and we are all perfectly entitled to feel the way we do.  It was gteat to interact with people especially the kids. They seemed to get a bit of a kick to see an old gal dressed like a pink I don’t know what...I’d see them looking at me or pointing me out to whomever they were with and so I’d give them a wee wave, and nine times out of ten they’d come back with their donation looking ever so proud. Just gorgeous! I have to say though standing for two hours was quite tough and by the end of it, my back was aching.  Not my feet which have to hold this weight up, but my back. Cripes, these last two collections, today and daffodil day back in August help highlight how bloody useless I am. Daffodil day I collected late afternoon, and was exhausted by the end of it and we were only there for an hour, so I decided volunteering needs to be done in the morning. But now after today, apparently I may need to be a ‘sit down’ volunteer. Anything else???? But anyhow, regardless of the aches I thoroughly enjoyed myself. I got to meet new people and make people smile.



After my volunteering, I met up with a friend for lunch and had a good catch up which was great. And so home to do a bit of housework and cook dinner, even had a couple of alcoholic beverages with my big girl before settling down to watch a horror movie. And thats Saturday gone. Another 40 minutes and it will be completely gone.

I am so glad to say this week has been a much better week. I have felt relatively human again, albeit a bit of a stupid one. Major changes happening at work and so the way we all do our tasks has completely changed. I will be using a completely different system as to the majority of those at work...just a small handful of us using it and so training to use it within a live system is quite scary. I know without a doubt I will pick it up but goddam it is so bloody frustrating for the moment. I want to know it all NOW! And because I don’t, I feel so damn daft. So I have been going home feeling completely frazzled and brain dead. But I think I have it relatively easy compared to the rest of the staff.

I was shouted to a Chick Flicks movie night on Wednesday night. We saw ‘Mountain between us’ which has Kate Winslet and Idris Elba in it. Brilliant movie - I thoroughly enjoyed it. I was bloody exhausted mind you, and my eyes were starting to get heavy but I managed to make it through to the end. And good golly miss molly, thats not where it ends! Hubby and I went to my cousins last night for a barbeque and a few drinks and yes, I even had a couple of red wines! It was a lovely evening spent with family whom I haven’t seen for many years, and getting to see a cousin and her husband while here from Brisbane. They were flying back home today. So all in all, it has been a pretty busy and social week for me. Admittedly, to go out during the week especially after being at work all day, sometimes I have to dig pretty deep to make myself go. Its not that I don’t want to, its just that damn word again ‘tiredness’. Once I get there, I am ok...its simply a case of getting myself there. Other times I simply have nothing left in the tank and have to stay home to refuel, definitely if its a working day the following day. But it really does make a difference getting out and not always being stuck within four walls. Doesn’t seem to matter which four walls they are, whether it be the lounge walls or the bedroom walls. They are a safe haven most of the time but can also feel prisonlike.

And so what does this coming week bring? I have an oncology appointment Monday morning followed by my usual infusion. I will go on my own as no test results or anything, so no necessity to take anyone to take notes. And that way, I don’t need to drop anyone off at home, I can go directly to work after its all done and cut down another hour that I could have been out of the office. Next weekend is a long one, so the prospect of a three day weekend is bloody wonderful!

It really will be the countdown to Christmas then...

Sunday 15th October 2017 - 12.05am

Sunday 8 October 2017

A slightly brighter Sunday

How bloody wonderful to feel so much brighter today! Its been a bit of a strange day I suppose. I managed to crash out again after publishing my last post here this morning, about 7.00am or thereabouts. I managed to sleep until 11.30am and woke up feeling quite refreshed. Had a shower, had brekky, kept up with those wonderful painkillers that I had taken earlier this morning and felt so much better, even having a bit of oomph for a change. 

Its just been a relaxed kind of day. I lay out the back on the outside couch propped up with a big pillow, playing games on the ipad, Ember (black cat) curled up beside me enjoying being outside - had my little radio on...just lovely.

Even cooked dinner tonight, cooked up my chicken pieces for this weeks lunches, took down the washing still hanging up - wow, what a difference a day can make.

Do I regret anything I said in my previous post? No I don’t...I’ve been feeling ‘invisible’ at work for a while now and sometimes I couldn’t give two shits and then other times it bugs the hell out of me so will just deal with that one on a day by day basis. I do worry though that I will say something that cannot be taken back. I can be very reactionary these days and say or do something that I will later regret. Done it a number of times already in the last 12 or so months.

I have always been a quiet, calm person who doesn’t really like to make waves and so when someone with a strong personality says something I don’t like or agree with, I will back down just to keep the peace. Well I don’t want to do that any more...why the hell should I? We’re all entitled to an opinion, so why not voice it.

But anyhow for now, I feel like I am back on track - what a relief. I feel like I am on a never ending roller coaster ride. 

I look forward to starting this week off at work feeling not quite so tired. I think keeping on top of the pain is a large part of the equation. Unfortunately though, the meds that work the best can make me drowsy. 

Speaking of drowsy, my eyes are starting to droop. It is quite late especially for me and I need an early start at work tomorrow - a big day with lots of stuff that must be finished, so will leave it there.

I bloody hope I continue to feel this good as the week goes on...

Sunday 8th October 2017 - 11.31pm

Lonely in the wee small hours

As I lie here in bed, its a little after 5.00am, I was up about a half hour or so to take some strong painkillers, I am hating on myself and this stupid cancer. I’m not scared I am going to die, not right at this moment although those times crop up, but my body is so sore and I hate it. Last night I wanted to break down and cry, simply with the frustration at this shell of a person I have become. I feel like I have lost my fun side...I am always so serious or feeling so damn intolerant of people.

Last night I told hubby I was bored. I was so sick of being stuck at home, even though that had been my choice for the day. I was wondering to myself, who could I go visit? And while I could think of a couple of people, thought they are probably out doing something or at home chilling with their spouses. I even thought about going to surprise some old ‘friends’ whom I haven’t seen for many years and certainly haven’t heard from since my cancer diagnosis but in all honesty, thought it was a little late to be thinking now about going out visiting, especially if I had to make the effort to look presentable. But I said to hubby, why doesn’t anyone come to visit me? But the answer is the same, everyone has their own lives, or they don’t felt like venturing out in the evening and usually when I do catch up with people, it is during the day.

My head isn’t in such a great spot for now, I am feeling quite down. Feeling worthless really. Feeling like a sad old lady, with no life. My girls are out doing stuff (and so they should be, they are only young), hubby gets to go out regularly to play darts and gets on the piss with the boys, my sister has her workmates and has drinkies with them...but what do I have, I have a sad, lonely life. God, do I even want anyone else reading this sad, pathetic bullshit??? I sound so ridiculous, whining about having no life but this journey is such a lonely one. It has placed limitations on me, the aches and pains I feel are so real and at the moment are making me feel pretty low. And I feel like no one really understands but of course that is true about any situation - until you have walked in someone elses shoes, you will never truly understand what they are going through. But when I see pics on facebook of people who are out enjoying themselves, I wonder why can’t that be me?

Old and pathetic...thats how I feel and nowhere more than when I am at work. I have been there since April 2004 and when I started, I was one of the ‘younger’ ones - probably mid range. Now as time has gone by, the older crowd have finished and as they employ new staff, they seem to be getting younger and younger. Is that a bad thing? No, of course not and the ones I have gotten to know at my office are all very nice young ladies. But because I don’t work directly with them and because I am a different generation from them, I feel invisible. Some make the effort to come and say good morning when they arrive, some say good morning as we pass by each other, others don’t say anything until we come face to face. Do any of them take the time to actually stop and talk to me, have taken the time to get to know me? No, not really...because I am one of the old bitches in the place, I’m not fun enough...and so sometimes in all honesty, I really don’t give a fuck. These people literally mean nothing to me and I don’t mean this in a nasty way but it is the truth....they are people who are employed at the same place I work, I don’t work with them on a daily basis - they are simply names and faces and at times I just cannot be bothered making the effort, because I know truly, they don’t give a fuck about getting to know me. Is this bad? No but it is hurtful because I think I am the kind of person who takes an interest in others...who always has time to lend an ear, but they simply see me as an old lady...too old to be of any interest. Should I care? Not really...I have the ones at work with whom I have a connection, why can’t that be enough? Because I am feeling so fucking precious right now. I want them to appreciate how hard it is for me to get up and come to work each day and just understanding that having terminal breast cancer and coping with fulltime work is not quite as easy as it is for them. And if people took the time to get to know me, would eventually see that I am an ok kind of person, who can laugh and joke as well as anyone else. Are my priorities different? Of course, I have done my drinking and partying - my priority is my family (actually probably looking after myself these days). But it takes me a little while to open up to people and let them in. But for those who take that bit of time, I appreciate it. I wonder if I will be a passing thought when I kick the bucket...or simply ‘out of sight, out of mind’.

And so as I lie here in the dark, hubby sleeping quietly next to me, one of the cats sitting on my little dresser next to me watching closely for signs that I will haul my ass out of bed to feed her, I can feel that those blessed painkillers have finally kicked in - thank goddness. Being in pain constantly is very wearying. To boot, it was a tough week as I said in my earlier post. My brother took sick early week while he was here at our place and I had to ring an ambulance. While they didn’t take him to hospital as he had already been at A&E earlier in the day, they reassured both of us that it was not life threatening but the anxiety my brother was going through was very real and I don’t mind admitting, it terrified the bejesus out of me. He is on the mend now thank goodness but as he is on his own, he really only has his son and I to ask for help. He was there for me when I was going through the original breast cancer stuff, running me to the hospital for my op, taking me back for check ups, not to mention the multiple times I had to go back to be admitted for numerous things. I envy his being able to go back to feeling his usual normal self and the joy on his face as he realises he is feeling so great is bloody wonderful to see. God we take something so simple for granted, until we don’t have it any more. For me, that is unobtainable...the best I can hope for is that my aches and pains will disappear for a few hours (apart from the cancer behaving itself of course!).

Summer is coming or is supposed to be coming soon according to the calendar and so hopefully with the warmer weather and daylights savings, I will be able to get out and about to do more stuff and be a bit more social. Hopefully my moods will brighten up. I think work is hard for me because in the old days, we were all a reasonably tight bunch and they always felt like my other family. Now it doesn’t...it feels like a place I have to go to each day to work and I am kind of sad about it.

A few posts ago, I was talking about how lucky I am to have so many people who love me, around and of course I am... all those people have their own lives or they live far away and we aren’t in contact all the time. And I do miss having a bestie or is it my idea or interpretation of having a best friend that I am missing? Over the years I have had very close friendships where we talked constantly, did things together constantly, even when the girls were little, we had close friends where we did things together with our families. Over time, those friendships have died, I lost confidence in myself big time and have never come back from it I don’t think. Don’t get me wrong, I have good friendships and I love them dearly - I don’t know. I don’t even know if I am making sense -in my head I know what I mean but having trouble expressing it properly. All I know is that I feel lonely...sad and lonely and I don’t like it. And I don’t know that I like admitting to feeling this vulnerable. I don’t know who reads this blog and so as I pass people, I wonder if they have read my deepest and darkest thoughts and what they think of it. Its freaky knowing people are reading your thoughts. Complete strangers is ok because I have no idea who they are...close family and friends because then they get an idea of what is happening and how I am feeling without having to repeat myself over and over again but I look sideways at people and I wonder “have you read it?” “What do you think of the thoughts I am spilling out?” But I remind myself, first and foremost I do this for me. It is such a release to get my thoughts out of my head. Sometimes I feel so heavy and weighed down by everything swirling in my head. I can’t believe how therapeutic writing this blog is. And while sometimes I have concerns about people reading it, it makes a huge difference knowing that someone is actually doing that. What they get out if it, I don’t know.

A close family member recently commented to me that she loves reading the blog...thats so awesome to hear but I wish I had asked why...sometimes I think it is too dark and depressing but having terminal breast cancer isn’t exactly a joyride. And as my cousin pointed out, people don’t have to read it. Your lucky, you get to leave the page if you don’t like what your reading...but this is my life. These are my thoughts and feelings felt pretty much on a daily basis. But what I want people to be aware of, is that when someone has a godawful disease, whether it be cancer or something else, while we may ‘look great’ as so many point out to me, the fears of your condition are always with you. It can completely headfuck you. I love hearing people say that I look great but I also want people to know that I don’t always feel so great...selfish of me? Possibly...

Sunday 8th October 2017 - 7.07am