Thursday, November 30, 2006
What have I learned from NaBloPoMo - there's a lot to say even when you don't think there is. I didn't get as much posted as I wanted to however - I'd really hoped to finish a bit more of my whole story of last year but it takes so long to write those posts and I have so many other things going on at the moment that I still didn't manage it. I will, slowly, obviously. I don't think I'm going to Holidailies - a brief respite is needed I think. Plus I really need to do things like write Christmas cards and the like.
I also haven't read as much or commented as much as I wanted to - I'm so bad. Bum.
All in all, an interesting experience and good for the discipline I think. It's been good for me to post every day I think and I shall try to make sure I post a little more regularly than I had been doing. So I guess all there is to say is that no kittens died because of me and
Watch this space.....
Wednesday, November 29, 2006
I do love the sea - the sea, not the ocean. The ocean made me very sick when we sailed across the Atlantic in December when I was about 11. On the Queen Elizabeth II, no less.
It was very luxurious but that's kind of beside the point when you can't leave your cabin because you keep vomiting. My brother spectacularly threw up in a potted plant as well as over the side. I just threw up in the cabin - I was obviously practising for chemotherapy.... Wow. That is so odd - to think of myself as that child and to know think that that child was going to get cancer. My dad didn't feel so hot either. On the other hand, my mother, who loathes flying, was perfectly fine and enjoying herself. She was known to come back into the cabin saying things like 'the waves are coming up to the top deck!' - really? Well, that's exactly what it feels like - funny that!
It was so rough that the first night out of Southampton they had to empty the water out of the indoor swimming pool because there were waves *inside* the ship.....
The dreadful thing was the fact that you couldn't escape it. It's the same with all nausea, I know - but it's so hideous.
Tuesday, November 28, 2006
I had some very sweet comments, which I wasn't fishing for, and I certainly wasn't criticising the few of you who do stop by and comment. But there are a lot of *other* people who, I can see from my stats, don't stop and don't comment.
But anyway, enough of that....
In fact, I have nothing to say today - I am too sad to hear about Laurie and the whole issue with my guides has blown up again...
Plus, it's my 3 monthly consultant check-up next week and I'm anxious. The phantom discomfort in my right leg is preying on my mind.
Enough. Enough. Enough.
Monday, November 27, 2006
I didn't even notice!
Howzat?!I didn't even know until now that there was a "Colossal Meal Replacement Bar" called the Big100 - but now I do! And so do you!
Actually, I didn't even know there was such a thing as a "Colossal Meal Replacement Bar" - and I'm really impressed that it's colossal.....I'd hate it to be all minuscule! ;) It's too bad I shall never be a muscle-bound babe now - no weight-lifting for me - all that lymphoedema fear and caution, you know.... So, I'll never have occasion to eat a Big100 - shame, they come in tempting flavours too: Apple pie, cookie dough, graham cracker - don't you just want to be a weight-lifter type person now?
Actually, to digress, that's one of the things you can't get in this country: Graham crackers (or plain Cheerios, or Annie's Mac 'n' Cheese - or Bernie Bunny as we refer to it in our household) Seems so silly, doesn't it? I also miss serious ice cream flavours - black raspberry, maple walnut, peppermint stick....mmmmm - yum. Also, no one here knows what jimmies are. And you can't get a raspberry-lime rickey. I must stop now - I'm getting a sugar high without having even eaten these things......
mmmmm - ice cream - what's your favourite flavour?
Sunday, November 26, 2006
People whizz by but don't stop - I'm not surprised; it's not a thrilling blog full of my exploits; it's not a 'baby blog' full of fuzzy photos and it does include the word 'cancer' fairly prominently on the first page which does tend to scare people away.
I don't blame people who run away from things cancer-related. Cancer *is* scary - we're all afraid of it really, I think. It's something living in us; threatening our very being and we aren't even aware that it's there for a while. If that isn't scary then I don't know what is. But we exist - people with cancer, people who've had cancer - we exist; and that cancer is part of who we've become and it's hard to ignore or pretend that it isn't. So. I'm not hiding it. So. Think a moment before you run away.
In nicer news - I got to do mass baby-cuddling yesterday - bliss. And I got to feed her. She's very bonny and so talkative! All these funny noises; grunts and things - sweet! I hadn't really noticed that in previous baby-experiences. Ooh, she's a clingy little thing too. She won't sleep unless she's held and ends up sleeping on her mum most of the night. I'm so excited to think that I get to see her grow up.
Saturday, November 25, 2006
Today holds a trip to that bastion of Swedish design - yes, IKEA.....
We need to order more kitchen parts since they've skimped on the number of cabinets and the like in the kitchen - V. POOR!
We also need to head to John Lewis for a new TV - the old one has finally kicked the bucket. Or, rather, is driving us mad with its turning itself off repeatedly and having a picture that resembles a striped deckchair. Bye bye TV! Do TV's have a happy hunting ground??
Oh, and I do yearn for a new, fantastic, enormous bed....ahh, space while I sleep - bliss....
All of this on 'Buy Nothing Day' Whoops. Perhaps we'll just look.
Oh - and it's a playing with babies day - yay! I get to meet my best friend's daughter for the first time this afternoon - she's 3 weeks old....more bliss.
Have a happy (non-shopping) day, y'all
Friday, November 24, 2006
It's also a year since my grammy died - on Thanksgiving Day last year.
She was a fantastic woman who I had great respect for; she had a real sense of adventure - she had a boyfriend who let her fly his small plane; she travelled in England and Scotland on her own a great deal and made friends as she went. In photos of her when she was young she was really beautiful. She wasn't scared to try stuff out - she worked in a hairdressers at one point and she was an operating room aide at another point. She loved little kids and whereever she went and saw kids she could attract them - the babies would smile and stare at her, mesmerised. She was a fantastic grammy - she loved my brother and I very dearly and would always bring us Cheerios when she came to England (you can't get the plain kind in the UK even now!!) and she'd send fantastic Christmas parcels with books and toys. But she would do fun stuff with us too - we always used to go and feed the ducks down at Winchester Centre and she'd take us to the library and to the Science Museum or the Chrildren's Museum in Boston. And when she came to the UK she loved to visit York - especially in the Spring time when all the daffofils were covering the banks. It was so sad when the Alzheimers took her over and changed her - she kind of slipped away and it was easy to forget that she was the fantastic person that she was. I miss the woman who always introduced us by saying 'The British are here!' and showed us off to all her friends.
Grammy, I miss you.
Thursday, November 23, 2006
Dial up! It is slow! I am going insane! It takes minutes to load webpages! Broadband and wireless - I miss you so......
The moving, it did go fairly smoothly....we are in - there are boxes - there is not enough space for all my cooking things in the kitchen. I already miss the kitchen that I designed myself. We can't figure out the timer on the boiler - strange. And the shower is even stranger with one tap working both the shower and the bath depending on which way turn it - bizarre, no?
We went to the pub for dinner and I cried - isn't that interesting? Me, crying? My word - because that never happens....
Must toodle now or the dial up will turn me crazy (er)
Wednesday, November 22, 2006
Damn and blast!
Plus I've just spent flippin' ages working on the flippin' question!
The great move has begun and most of downstairs has been moved to the new house already. It's looks much bigger with no furniture and books in it! Perhaps that should have been the solution - no belongings!!
This is short and sweet because it's late - it'll probably be short and sweet tomorrow too because it's back to dial-up (OMG! Dark-ages! Broadband, we love you! And wireless! Don't forsake us - please get connected quickly!)
Tuesday, November 21, 2006
Monday, November 20, 2006
At my next clinic appointment my consultant decided that after the rest of my chemo treatments I would have G-CSF injections - they are a growth factor that stimulates the bone marrow to make more white blood cells; which, of course, are one of the things that the chemo kills off, leaving you with little protection from infection. So, for five days on the week after my chemo treatment a district nurse would come to my house and give me a Neupogen/filgrastim injection. The district nursing system is a fantastic thing. I paid nothing for this; I would just telephone the DN office or the nurses from the chemosuite would send them a fax with the dates I needed the injections. I would be given the prefilled syringes to take home with me after chemo along with my pile-o-drugs - also all for free. And they would live in my fridge - they had to be kept cool for the week and I had my own sharps box for the syringes which lived under the sofa (of course!)
So, the first Monday morning after my second round of chemo, Mark turned up. Mark was a very sweet, Scottish (I'm a sucker for a Scottish accent), male (in case you hadn't noticed) district nurse. And he was a sweetie, made me feel much better. Asked about how I was feeling and did the injection for me. I point-blank refused to do them myself. Various people kept telling me I could do them myself. My reply was that if I wanted to stick needles in people I would have gone into the medical profession and that there was a reason I went into libraries. I didn't see why I should do them when there were all these people who had been trained to do it!
So I had a lovely mix of nurses over my six months - a couple of great New Zealanders; Ema who just made me feel so much better on one of the days after Taxotere when I felt like I'd been beaten black and blue with a baseball bat and was practically in tears with the pain in my back and numerous others.
I resolutely never looked when they did the injections - which went into my abdomen. They were always quite uncomfortable because they would sting as the liquid went in - the needle prick didn't bother me so much as that stinging did. It was always interesting to see who was the best at giving those injections - I definitely used to be pleased when one particular nurse turned up because she was brilliant - I don't really know what she did differently but I would barely feel a thing when it was her. I liked having the district nurses come because it made me feel a bit safer - that there were people who knew what was what seeing me at the time when I was most at risk of the neutropaenia coming back and I suppose I felt that if there was any problem then they would recognise it and send me off to the hospital.
The other outsome of the neutropaenia was the strict instructions to use Corsodyl mouthwash several times daily to prevent ulcers or cankers or other sores in my mouth. This stuff is weird, I was given the mint flavoured variety and after the first taste I just thought, mint. After I spat it out I thought, ooh, zingy and then I thought 'yuck' - It seemed to mix strangely with the vile taste I already had in my mouth and made everything taste even more peculiar - including water. So, I was really unwilling to use it: but I did. And the only time I got a mouth ulcer was when I didn't use it for a few days because I had run out. I started using it pretty sharpish after that and was very grateful not to have anything worse go on with my mouth. To be honest, the bad taste was so horrible I was glad not to have any further complications. I just felt like I was in a permanent state of feeling like I hadn't brushed my teeth for months, even if I'd just cleaned them; and nothing tasted right. Everything just tasted strange; I stopped drinking tea and coffee: I just didn't fancy them - they didn't taste good enough any more. Chocolate and sweets went - sugar seemed to leave a really horrid aftertaste in my mouth - probably why I lost weight throughout my chemo treatments. If only I hadn't put it back on again. And I stopped eating cheese because someone told me I shouldn't eat things I really liked while I was having chemo because it would put me off them. Funnily enough, I don't really eat cheese at all now and I used to eat it by the bucket-load.....well, quite often. And no, I haven't given it up because of the whole 'don't eat dairy, it gives you mucus and cancer' thing. I just got out of the habit.
Anyway, so that is the story of my lovely district nursing team - thank you, y'all!
Sunday, November 19, 2006
I am exhausted, they are exhausted - they were up until gone 11 last night doing activities and then they were hauled up again at 6am this morning. We were running activities until 11 last night, then we had to de-brief those sessions and touch base on today's activities so it was 12 by the time we were done, 1am by the time we got to bed and I dread to think what time it was by the time Sarah stopped talking..... Bless her, I love her dearly but she is a real night owl and I am easily led astray except I haven't got the sticking power or the stamina to cope the next day. So I am ready for my bed.....
They're a nice group - when I saw the list I was happy straight off with who we had on our trip. They'll all be at least 15 by the time we go and they've nearly all had some international experience before. So, that's reassuring for us - I swear, some of them have more experience than me!
I think they'll gel together as a group fantastically by the time we go and they'll be in floods at parting when we get back. It was so interesting to meet the international groups from this years trips on Saturday - they were so much more confident and grown up. You could just see the differences. Our girls will learn so much from it - I wish I wasn't so scared about it all.
Must sleep - have to work tomorrow!
Saturday, November 18, 2006
Today is the day I meet the girls we're taking to Peru next summer.
I am running late, so if I'm not careful I'll miss the bus and then miss the train and then miss the start of the GAINING training.
So, t'ra - cross your fingers for a group of nice girls for me!!
Friday, November 17, 2006
And at the moment I am feeling even more consumed by the past. It is a about 2 weeks short of a year since I finished my treatment for cancer and I am acting like it was yesterday. I feel ashamed that I am not 'better' - not a better person for not being able to put this down and get on with life. Like a part of me is hanging on to this. But I do feel so sad - you know, that stomach-aching sad; that bottomless pit sad; that weighed-down sad.
And I have to get up at the crack of dawn tomorrow to get to this selection weekend and I haven't finished packing - I have done some, which is good, but not all.
I don't think I'm ever going to feel better.
Thursday, November 16, 2006
But I would debate this - I think fear is one of *the* most human traits. It's part of our animal nature and I don't think it really disappears because we have a belief in a god or other spiritual being. It's an instinct - and I don't think they can be governed by the logical mind.
Am I frightened? Yes, of course I am - but what does that mean? Well, what am I frightened of? The cancer coming back; dying; not getting to do all things I still want to do; my family and friends being sad; pain; having to go through all that treatment again. Why is all this frightening? Well, it seems to me that it is proving just how strong my instinct to stay alive is. But it is instinct - not logic.
I spent far too long today grokking out on Laurie's blog. I just got sucked on in there and was reminded so many times of what I experienced. It's very bad - I shouldn't do it because it confuses me. I get muddled about where I end and where other people's stories begin. A very strange trait I feel.
This is all very dull - I feel it may be time to stop the waffle.
I'd like to say it'll get more interesting over the weekend but I fear it won't (Well, it will for me because I'm going to meet my Peru team but it will mean short and sweet posts late on Friday, early am on Sat and curled up in a comatose heap late on Sunday - never fear! I'm not letting NaBloPoMo get the better of me!!!)
Wednesday, November 15, 2006
I've been looking at my stats recently and I am saddened by the number of people who come to my site by searching for information about portacaths. So many of them stop by and read a few pages and then disappear without commenting. And to each one of them I want to be able to say 'I'm so sorry' that you're in a situation where you need a portacath. I don't want people to have to go through the kinds of things I went through andI wish you would say something so I could know something about you - because otherwise my imagination fills in the blanks.
I 'met' another BC blogger today - Laurie - and I flicked through a few pages at the start of her blog when I wasn't working today. And, as so often, reading her diagnosis story reduced me to tears. And I was interested that she, like me, had written a post about what and what not to say to someone with cancer. I suppose it's not that surprising - it is hard to say the right thing and sometimes there isn't a right thing; but.....interesting. As I say to people I meet who've had breast cancer - I wish I didn't have this in common with you; I wish I hadn't met you because I wish that neither of us had had to go through what we have. But we have. And I'm very grateful to Kim for her comments and her insistance that I am a strong person. I find it hard to see that because I'm the one wallowing in my own head; and I am wallowing at the moment, I am overwhelmed by myself and lost in myself. I'll get out of it - I think Elaine's hope is rubbing off on me; I really do believe I will - but I think it's going to take a while.
Tuesday, November 14, 2006
SO - tonight you get a picture post - you may not want to know what I had for lunch but you definitely want to see a picture of the cat, right? No? Tough!
What a sweetie, right? No! He is a fiend who will lurk under chairs, on sofas, on stairs and suddenly attack. He is your ankle's worst enemy. You have two anyway, so you can donate him one, OK?
He is the terror of cardboard boxes, which he shreds into a state of collapse.
He adores the printer and likes to stick his paw into where the paper goes in because there must be something good in there to be making those noises.
He is also a huge Creature Comforts fan - he races up to the television and stares at it, entranced when we put the DVD on.
So, I present to you - Maxwell the cat-fink!
Monday, November 13, 2006
The Royal Albert Hall.
I've sung here.
I never got round to telling y'all about it though - what a zizz eh?
I not only sang here, it was for the Proms and it was a premier.
It began when a friend forwarded me a link to the Beeb site asking for singers to apply for something called 'The Voice Project'. They were looking for London and Glasgow-based amateur singers to take part in a collaborative performance with The Shout of a new piece by Orlando Gough.
I filled out the form and didn't expect to be selected - but in the end I received an email inviting me to take part. I was very excited; especially since morale was at a low level then (what, as opposed to now, you mean?)
The rehearsals started a month before our proms (we did 2 concerts) with a weekend workshop with 3 members of The Shout: Carol Grimes, Adey Grummet, Melanie Pappenheim; and they were great - really fantastic.
They not only had incredible voices but were really enthusiastic and innovative in their singing. And what was really exciting for me was that I had met and worked with Adey Grummet before: at an Opera North summer school when I was 15 - and she was just as energetic and entertaining as I remembered her. She was also very kind when I went up to her and rambled about how she wouldn't remember me but we'd met before and I'd really enjoyed working with her then and now. She was kind enough to say that she thought I looked familiar - I suspect that may have been a kind white lie; I think I look quite different than I did then - curly hair and all....
The piece was really interesting and very compelling as well. I was part of the 'London Rabble' and the parts we were singing were mostly nonsense/made up words with a vew 'verses' - the choirs were singing the comprehensible parts with The Shout filling the solo/small ensemble sections.
The Shout were utterly fantastic to listen to - they did a couple of other pieces during the concert and I was just enthralled to listen to them - one of the pieces 'Stand' was just *brilliant* and I had it running round my head for days afterwards - I woke up in the night with it running round my head. I would love to sing like that; as part of something like that.
It was quite a bizarre experience being in the Royal Albert Hall - people who had sung their before kept saying how huge it felt and how seeing that many people could be a bit unnerving so I was quite surprised when my reaction to standing on the staging and in the promenading space was that it felt a lot smaller that I expected. So I thought that maybe once it was full of people - then it would seem bigger - but no, it seemed smaller again once there were audience in it - it just brought the levels and layers closer down towards me. I wasn't nervous, I wasn't freaked out; but neither was I excited by it. And that is a big sign for me that I am obviously not really 'well'. I ought to have been excited or proud or happy or at least faintly pleased - but I just wasn't. Perhaps that's why I haven't written about it before now. I felt 'dead' - like I do about so much now. Like I've never come out of the anaesthetic - I'm still numb.
Sunday, November 12, 2006
I look at this photo and I see the tiredness in my eyes; the 'deadness' - it's like I'm not there. And although, at this time, things were tough - I had no inkling of just how tough they were going to become. Or, indeed, how much sicker I was going to look by the end. I don't have many photos of me once my hair came out and I started to look really ill - really like a person with cancer. By that point none of us really felt like taking pictures - we didn't want to remember that time; we didn't want to be in that time.
Today as I type this - I am sitting in exactly the same place in my flat, with the same blanket over my knees. What's changed? A lot, a little, nothing? All of the above? Probably.
Some things have gotten better, some have become worse.
I loved this haircut and I wanted it back - but now of course my hair is different again. I can't keep up!
Saturday, November 11, 2006
OK - so that is what I was going to do - but the computer refuses to find the camera - I loathe you, computer! I wish you to know this - ::deep loathing::
And I was going to show you the sweet little baby sweater I've just about finished - it's just waiting for a zipper since I decided I didn't like the toggle button fastenings from the pattern. It has a hood - very sweet. And is destined for Ffion - my best friends 2 week old daughter; who I have yet to meet since she's all the way away in Wales.... :( Hopefully I'll see her before Christimas though - I do want to see her while she's still little. I missed her birth by a matter of days since I was visiting the day before my friend's waters broke - Ffion decided to make an early appearance - by two weeks. She's obviously a performer, like her parents! ;)
Ah well, that's it for today since I've been scuppered and have wasted all this time faffing around with the camera - it's bedtime and then some!
Friday, November 10, 2006
The fireworks are going like mad again even though Bonfire Night was last weekend - they seem to have been going on for weeks because it was Diwali a few weeks before too. I like fireworks - I have fond memories of Bonfire Nights at the top of the garden of some friends. Fireworks and sparklers and hot soup and baked potatoes in the fire and sausages in buns. Until they moved away, anyway. Then we used to go to the public display at St Chads and have chips from Bryan's Chip shop on the way home - my fingers would be freezing because I'd taken my gloves off and the chips would be boiling hot and burn my mouth. And I would tuck one hand round my dad's arm which would keep in a bit warmer.
The bonfire would be built of old branches and old bits of wood or old doors or planks or, I remember one year we burnt an old desk. But before you lit it you would always take the bottom apart a bit to check for hedgehogs who like to snuggle down in the pile of wood and would get burned alive if you didn't scare them away - poor things.
It's amazing how loud and bang-y the fireworks seem to be now. Sometimes when I hear them just for a moment I think it was a bomb - especially living in London, you worry about these things. And I wonder if this is a tiny bit what it was like for my grandparents living through the war. Banging and flashing in the distance if you were lucky - rather closer if you weren't lucky. I wonder if my grandparents ever felt entirely comfortable with the experience of Bonfire Night after the war. I remember my grandma getting rather upset when my brother and I watched whichever James Bond film ends with the massive fight in the submarine bay. My grandma spent at least 2 years of the Second World War without hearing from my grandad who was driving around the Middle East and was injured. I mean, can you imagine that? Not hearing from your husband for over two years and not knowing where he was or how he was? I find it mind-boggling - I have so much respect for the men and women who lived through that time and I am so grateful that I do not have to go through that.
Don't forget tomorrow when at the 11th hour of the 11th day of the 11th month we will be silent and remember those who did not come home to their families; to their wives, to their children, to their friends.
Thursday, November 09, 2006
How do you feel about the green? Too much green?
Green is my favourite color and I'd love a verdant, leafy look to my blog but that would require knowing a heck of a lot more about this blogging lark than I do. Maybe one day when I'm not doing a trillion and one other things I'll work it out......
SO, green, comments please.....
Still grieving apparently.
It keeps catching me by surprise. I keep thinking I'm done with the crying and then it starts again. I keep thinking I've accepted my lopsidedness; my scar but then the grief gets teased out and the tears come again.
I think I've finally found my anger though - I'm left being angry with the cancer because there is nothing else to be angry with. How dare it come into *my* life? How dare it take *my* breast? How dare it grow in *my* body? And it will never be gone - even though the growing cancer has gone (I hope) - its repercussions and its memories will never be gone. I cannot define myself without it. You try it - you try looking at yourself with a scar like this - or any major scar. For better or worse, it's you and you (I) have to accept it and you have to get on with living life - but you don't like it, the whole way you feel about your body changes. I don't like the way I look, I don't like the way it feels to have one breast, I don't like the diagonal scar - although it's as smooth as silk after all bio-oil it's had put on it. I don't think I'll ever be comfortable - I think there will always be an underlying hatred of it, and it's hard to hate yourself.
In other news, want to see a picture of the new house?
This is the back of the house. Doesn't look like much really, does it? But it is nice....I promise. More pictures when we get some furniture in it.
Wednesday, November 08, 2006
It's a shame that I'm not a better swimmer because I am a bit of a liability in the pool. I am one of those wimps who doesn't like to put their faces in the water - I panic. Guess what!! Something else I'm fearful of! Drowning at the swimming pool! I'm a challenging woman! (See! AJ was right!)
Fortunately I managed to go in the middle of the day before it got busy and/or full of kids swimming lessons. Unfortunately one of the people there was one of those terrible splashy-crawl swimmers. Poor style!! I shouldn't comment since I mostly do a bad breast stroke or a frantic doggy-paddle - but at least my swimming style doesn't cause other people to end up choking on my wake. Grrr.
I hate water up my nose and down my throat and I really haven't got the hang of it.
I can't help it, I come from a family of reluctant swimmers.
My one memory of swimming lessons as a child is in the very baby pool at Holt Park and as far as I remember we were just striding across the pool - water at thigh-height.
It obviously was of limited success. I gained my 50 meters certificate at school and that was an effort. And I'm still not the most confortable of people in the water.
Plus, I now wear the most blah swimsuit ever - black, polyester, high necked, low legged, tummy control. Because of all the pockets and lining for keeping my prosthesis in place I feel like I'm in a strait-jacket or an iron suit (whatever one of those is...)
This is obviously not me and the snazzy beach background takes away from the drabness of the suit itself....it's streets away from the turquoise, flowered bikini that I used to wear (topless) when I worked in Chania. Just another thing that breast cancer has taken from me, besides the pound of flesh. Well, several pounds-worth I should think.....
So, in an effort to improve my swimming, I bought a book. Stop laughing. It's not that funny. Yes, I bought a book in order to get some swimming tips. No, it's not waterproof; no, I didn't take it to the pool with me.
I know it sounds silly - but it's called "Swimming without stress: lessons for land lovers" - sounds like me, yes? And it's based on Alexander Technique; which sounds good to me and it's about being confident in water and releasing and swimming without tension. Sounds like just what I need.
Sadly, I didn't get on well with my attempts to practice breathing into the water. I fear I may actually require someone to be there, in person, to tell me what to do and to haul me out when I half-drown myself by panicking in the water (which I'm sure is half the reason the water spouts up my nose - unless it's some magnetic thing.)
I have to get the hang of this swimming thing. I'm a pisces, for heaven's sake! It's embarassing! And I do like being in the water, as long as noone else is making ripples or waves.
So, if there are any London-based swimming teachers who subscribe to this sort of teaching/swimming method, please drop me a line. I might be prepared to shove a little cash your way if you'll help me out. (What're the odds of that, eh?)
Tuesday, November 07, 2006
Other people don't see the inward struggle - they see that you've finished your treatment and they see that as the end. They've wanted you to be better for so long that they move you into the 'better' category. I haven't worked out how to say - I may not have cancer anymore, but that doesn't mean I'm 'fine'.
Monday, November 06, 2006
Sunday, November 05, 2006
I would not know Prada if it came and bit me on the ankles and I certainly couldn't walk into a shop selling it because I would be far too intimidated by all the smart people and certainly couldn't walk out again if I bought shoes without going arse over tit.
This film annoyed me a great deal.
Mostly because this film was trying to pretend that it was telling some great moral tale about how being fixated on fashion and how you look resulted in unhappiness; sadly, for me, it failed. Because despite the fact that, yes, she did give it all up because she recocognised it had changed her into someone she didn't like - the fact remains that there were lots of undercurrents.
For example: dressing prettily and being fashion-concious gets you a man with lots of money and influence
Fancy shoes and clothes mean people respect you
So on and so forth. And these things were there in abundence in the film and I don't think that last 20 min turnaround was enough to negate those messages.
Saturday, November 04, 2006
This is a little of a cop-out post because it's actually what I wrote for the Pink for October site but I think I'd like to share it here because I did take some time over crafting it. It's not a pretty story - but then, so much isn't.
September 29th 2006:
One year, seven months and 3 days ago I sat in a small room in an NHS hospital and heard the words “I’m sorry, it isn’t good news, it is cancer.”
This was two weeks before my 28th birthday. I sat and I stared at a metal cupboard in the corner and I thought “Goodness me, I hope I wake up soon because this is the worst nightmare I’ve ever had. This can’t be true because I. could. not. cope. with this.” But then, it was true and so I said “Well, that’s a bit of a bugger, isn’t it?”
So, from that point the journey went on: through AC and Taxotere chemotherapy, through “febrile neutropaenic sepsis” with IV antibiotics and a 5 day stay in isolation, through a portocath insertion that initially refused to work, through a mastectomy, extensive ‘jollying’ physiotherapy, through radiotherapy, Tamoxifen and Zoladex. Through uncertainty, fear, pain, tears (alright, hysterics) and depression, the journey wended its way. Wound its way through to a day one year and 18 days ago when I came round from anaesthesia knowing (hoping) that along with my breast, the cancer had gone.
The two, interlinked – something I loved with something I hated; something safe with something deadly; something that was part of me with a thing that was invading me without pity.
I spent the intervening time – six months – trying to assimilate what it meant to have cancer; trying to learn how to be someone with cancer. Someone with no hair, no eyelashes, no eyebrows; someone who could barely walk round the block; someone whose collection of medications made them look like a pharmacy – or a drugdealer (anyone for domperidone? I have enough to last a lifetime but, sadly, they didn’t work for me!); someone living with a lump that was trying to kill them.
And then, (now), then(now) it was(is) gone and I had(I’m having) to learn that too – how to be a person without cancer, how to be a person who *had* cancer. Do I still have cancer? They tell me I don’t, but how do they know? How can they know that there isn’t a small cell lurking somewhere in me, just biding its time? In four years – if the cancer doesn’t come back in the meantime – I’ll “officially” have beaten it. My risk will be no greater than anyone else’s. How will I feel then?
My fear is that I’ll never believe it’s gone and will live the rest of my life with a mental scar as prominent as my physical scar.
Friday, November 03, 2006
You probably will have noticed this fact. I feel so much better for not being bright pink but feel that the subtlety of the plain white-ness - i.e. no colour at all - looks a bit dull now. And I'd like to think I'm not as dull as all that.
But I don't really think much of the other colored designs on offer at blogger so I don't know what to do..... Any ideas?
I also wanted to say that I will be making a policy of commenting on at least one new blog each day for the duration of NaBloPoMo - because it's nice to comment, isn't it?
But what is the etiquette with commenting?
When someone comments, do you write back and say 'thanks for commenting' and then do they write back and say ' no problem, you're welcome' - at what point does someone *stop* responding? Or don't you respond at all in the first place? I don't know the rules - help!
Thursday, November 02, 2006
Or, it would be if I knew anything other than what I read on Wikipedia about her; but I think I may need to know a bit more about what she thought.
Today I have been thinking about my identity as a woman or my lack of identity as a woman. I abhor all 'girlie'-ness and somehow feel it is a sign of weakness. Being female is to be weak and vulnerable; it does not comand respect. And so I am not allowed to plan a fantasy wedding or pick out my children's names or look at engagement rings. I am not allowed to wear dresses or make an effort to look pretty. If I wear makeup or dress smartly I feel like I have to put myself down. I hate to cry and be emotional or irrational.
Imagine how this confusion over my female identity has been affected by the loss of my breast.
You must understand that this is in some strange instinctual part of me that I feel this. It is not what I logically believe to be the case and it is not the way I think women ought to feel or what we or I should believe.
I believe in equality. But somewhere underneath I am undermined by myself. And I have no idea where I have learnt this from. Not really. In a roundabout way - I think I've always tried to behave in a non-'girlie' way and somehow that has had the effect of teaching me that to be female therefore must be 'bad'.
Apparently, Luce Irigaray started to say that that women could/should be equal for what they were, which is different to men. But that society did and does not recognise that. I believe that the 'third wave' feminists are the women out there who are saying that feminism is actually about choice - it is about choosing which elements of femininity to embrace. Which, I think, is what some 'mommybloggers' out there are saying - especially SAHMs who counter the arguments that they are undermining the work of feminists gone-by who fought to get women out of the home and into the workplace. That actually, being a feminist is about having the choice - of choosing or being as female as you wish.
But I can't be a woman - I haven't got the right shoes.
Wednesday, November 01, 2006
My parents had rung David to let him know what was going on - poor soul - I think he must have been so scared - he wasn't in London and couldn't get down to see me that day.
After a while, Keith came by - he was his usual cheerful self - nothing seems to throw him. He massaged my legs and feet which was strangely reassuring. I think it's a human-touch thing - it's comforting and reassuring to be touched. We are tactile beings and we need to feel connected. Keith offered to lend me his CD player and a couple of relaxation CDs after I told him what was going on - he could see, anyone could see, that I was in a total state.
Eventually Ivy comes by - she's another reassuring sort but she explains that the chemosuite is really busy so we'll have to wait until things have quieted down a little.
So we carry on waiting - it's amazing how much you wait.
And the sun moves round and streams through the window and it gets hotter and hotter and I was already hot to begin with! One of the nurses finds a fan which stirs the air around a little.
Finally Ivy comes back - this time my parents are allowed to stay in the room. She has me lay down and she starts to feel the whole area around the port - trying to feel where it is and how it's lying - I am like the proverbial board, and so tense; I grip my dad's hand and he tells me to squeeze, hard. Every time Ivy presses or touches the area it's all I can do not to writhe and wince. It hurts, my shoulder is so stiff and I don't want anyone to touch it - but I let her. Once she thinks she's found the right place she puts the needle in - when the needle is put in it goes through the skin and punctures a silicone rubber bubble covering a chamber which connects to a catheter which is connected to a vein. The bubble is self sealing, so when the needle is removed, it seals over.
Unfortunately because mine is so new, I'm still bruised and sore so the pressure of the needle going in presses the base of the portacath back into an already sore spot. The needle goes in, but again, nothing is coming out. I'm freaking - I have this foreign object inside me - freaks me out already and in addition, it's faulty, it doesn't work, it hurts, it's all bad, bad, bad!
Ivy tries to move it around, pushing it down, moving it around slightly - it's excrutiating, every time she does it a shot of pain goes through my shoulder - I am brave, I lie there and take it and squeeze my dad's hand and try not to gasp too much but I can feel it catching and grating. My mum stands at the bottom of the bed - holding my foot. I think she must have found it very upsetting - it's hard to see your child in pain and not be able to help. After about half an hour Ivy says that it seems to have been put in quite deeply, that the stitches are in the way and that it's quite swollen. She thinks the problem is that these factors are preventing the needle from going far enough into the port - she wants to try a 1" needle. However, she'll put some Ametop cream - a topical anaesthetic cream on the area to try and decrease the pain somewhat. The cream has to be on for 45 minutes before it really takes effect so Ivy goes away for her lunch.
I can't remember that time really - other than a feeling of sheer and utter panic - I often described the way I felt last year as 'twanging with anxiety' and that's what it often felt like - I was so wound up and tense with anxiety that I felt like the vibration and sound and tautness of an elastic band stretched out as far as it will go. I was at snapping point for a year - I never knew if I was going to completely lose the plot from one moment to the next.
Ivy came back, she cleaned off the cream and put the new needle in - it still hurt. I think it was the underlying bruising and pulling of the stitches that hurt more than it was the needle going in. This time a little bit of blood pulled back out into the syringe but not much and it was hard going for her - it still wasn't really working. Ivy did move it around a little more, with no better results. Eventually she said that she wanted to stop - she could see how much it was hurting me, it wasn't working properly - probably because it was swollen and the stitches were still in. She would put in a cannula for the antibiotics and we'd try again another time. She didn't want to hurt me any more.
She redressed the portacath site and stuck my hand in hot water to bring up the veins and put a cannula in the back of my hand. Which she did beautifully, without a hitch, so that I barely felt it - why couldn't they have done that in the first place?
Nightmare nurse came back and injected the first lot of antibiotics into me - it felt cold in the back of my hand and up my arm but hopefully they would start to do their job.
They still had no idea where the infection site actually was.
This is part of the view I could see from my room.