Showing posts with label chemo. Show all posts
Showing posts with label chemo. Show all posts

Sunday, 20 January 2008

2007 Dec 6th - Last chemo!

Thursday, December 06, 2007


And now.....the end is near....and so we reach .....the final CHEMO!
Category: Life

I feel like Arkwright at the end of an episode of "Open All Hours"........

It's been a funny old week. If it was a tarot reading the Death card would definitely be in it somewhere.........the end of one phase and the birth of a new one.

Monday was Beating Bowel Cancer comedy night at the Comedy Store in Picadilly (London for all you northern cheeky monkeys, who think that's yellow stuff in a jar). I put on a frock, some legs, my new boots (superb bargain under £20 with more than a hint of FMB about them) and some jewellery. My hair underwent the GHD/After Party treatment and Beckie came by to take me to my final "am I fit enough for chemo" blood test .........or so I hoped. No stroppy women in pathology this time and then it was back home to await Thomas the Tank's stunt driver (Mike) who was moonlighting as our chauffeur to Laaaaahndan. Actually he was on the guest list, but stupidly volunteered to drive!

In true grown up stylee I littered the entire journey with criticisms of Mike's driving (so he could taste married life without the expense of divorce) demanded we stop for a wee wee, food and whiny requests as to whether we were "there yet".

Cockfosters for free parking (thank you blue badge), freezing cold train station and about a zillion stops later we arrived at Covent Garden.............not before having an emergency stop at Arnos Grove.

Mike wanted to stop at Arsenal on account of I have Nil Arse (think about it) but my bag was about ready to explode, it was making me look like Sigourney Weaver, with hair and make up, in Alien. In desperation I flashed my "the bearer of this card has a medical condition.............needs to wear medical appliance........toilet............URGENT" card at a small, unchatty rail employee who silently unlocked the female staff toilet.

Emergency averted........no bag contents running down my tights into my beautiful new boots!

Back onto the tube, chilli con carne for me in the Garden (it's relevant it was red meat). Met Angela and headed for the venue.

Firstly I spotted Faerie, hard not to she's got a mahoosive grin! A very teeny weeny umpalumpa sized Faerie she is too, hugs for her and a much healthier looking Caz than I expected!. Lizzy, another bum bandit, (s)mother and Katie from BBC.

Managed not to cry, was quite keen on getting to the bar to be honest! Stupidly FORGOT to get photos which was just soooo dumb, but we all forgot so blaming the excitement!

Faerie and Caz did their speeches without fluffing, falling off their high heels, the stage or any wardrobe disasters. I just about held back the tears and had a little sister hand to squeeze when it was hardest.

Three beers, some wedges and dips, four comedians plus a very nice compere, later I was stuffing a MacDonalds down my face (more red meat) including a Festive Pie.........it was the beer alright?

After picking up one of Mike's friends and her suitcase after her holiday we were at last on our way home, tired and weary but having all had a jolly good time. I got to bed at 2.49am........I arrived at the chemo suite Tuesday morning at 9.03am.

After four paces into the chemo suite Lisa (the sister) said "You look gorgeous........don't go any further". Oh SHIT. Here we go again. My neutraphils were still at 1.3 as of Monday afternoon. Now considering the length of time and amount of injections I've needed to stay just above 1.5 we were all resigned to me failing the test after only a few hours. All was not lost though, onco Tom said if it was too low that was it NO MORE CHEMO for me, we'd just abandon the final one. After proclamations of love for Lisa, Tom and the entire nursing staff we trotted off to pathology again.

Now by this point I was almost bouncing off the ceiling with excitement because it meant I could be spending the day with my "special chemo guest" without the evil drugs and WITHOUT the PICC line when my blood test came back at 1.4 or something.

Lisa didn't change my dressing, expecting to be removing my PICC line. Ray appeared with the A4 white sheet containing my blood report........get this.........

TWO POINT EFFING ONE!!

Seriously!

I thought he was winding me up.....or got someone else's results......after believing I was going home never having chemo again, to be told I was fitter than ever and would be having this one more treatment was very weird. The only conclusion we could come to was laughter, beer and red meat had bounced my bloods more than neupogen could, or maybe it was the excitement of meeting bum bandits, my special guest, being with the three people who have done the most for me this year (Beckie, Angela and Mike), the excitement of completing another round in the boxing championship against Tyson.

Mad.

Special guest arrived and swapped duties with Beckie, getting me tea and minstrels and generally making me laugh. Lisa had brushed her hair specially for the visit!

Back home for take out pizza! Not recommended for chemo patients but I was riding high on the blood results and general good mood and company, and was too lazy to cook.

Fast forwarding to today. I bought cakes for the nurses (two each) and sat and waited til they were ready. I didn't need a seat, just the bed! I gave Lisa a hug who seemed really small all of a sudden and she said she'll miss me. My eyes hurt a lot from the tears (stupid side effects). I promised to pop in and say hi whenever I was visiting for check ups. I took a couple of final photos of my right arm whilst I waited for Izzy which are in my Cancer Fings folder.

Not knowing quite what to do next I ordered a bouquet of flowers for my special little sister for all she's done over these chemo months, not just the driving, I think that was the easy bit - we just had an excuse to sit around chatting and drinking tea. It was more for the support, the housework, the offers of help repeatedly even when I repeatedly turned them down until I gave in and admitted, yes I do need you. It was for the unlimited supply of chai and sympathy, the ironing, the child care and sounding board. A comparitively small gesture, a bouquet, an orange Options sachet each and a packet of hob nobs for her tea break at work, but it was all I could think of in the chemo fog.

Feeling very sick today, a bit lonely but now I have a warm feeling where there was just a cool feeling of hope before.

Slept a lot this afternoon and have that "I just swallowed a whole apple and it's stuck in my throat" feeling that won't go away, spazzy hands and dodgy vision that day three usually brings.

I've missed a few bits out......but those of you who know what I'm talking about can always message me privately for gossip and details .

I still find it hard to associate myself with cancer sometimes. Since I turned a corner mentally I don't feel like a patient and I've never felt like a victim but should I keep reminding myself I've been through some serious shit? Part of me wants to forget but another voice says, bury this at your peril cos it'll come back and bite you on the ass all the harder if you do.

I'm sure I've said this before, but I'll say it again. I would rather go through my surgery again than chemo. It comes second to radiation, not least because I am still suffering from the damage from that, not to mention the menopause etc.

With surgery you improve daily, maybe fall back a bit, but always in an upward trend. Chemo is a downward trend of ever decreasing peaks and ever increasing troughs. It saps the very will from your veins to do or think anything on a regular basis. Looking back I'm glad of the blood troubles I had now it's over, it meant I had additional recovery time and subsequent treatments didn't hit me as hard.

The desperate lows I had in my hospital bed after I left critical care, where I couldn't eat, wouldn't eat, didn't care about the fact that I couldn't eat. I've had those on chemo. The tears of hopelessness about my new body, the unfit, unnatural one that replaced the relatively well cared for one I had before - had those on chemo. Lethargy, nausea, depression, cold sensitivity, leg pains, hip and knee pains, lack of balance, dehydration, poor nutrition, diarrhoea and leaky bags.........none of these things are condusive to excercise or maintaining muscle tone.

But it's over, I am saying every mantra and doing every mojo dance in my head that I NEVER have to go through this again. I'm doing the same for all of you who are still in the middle of it or about to start. Hang in there.

Chemo 19th February 2007 - 6th December 2007 RIP.





22:15 - 7 Comments - 6 Kudos - Add Comment - Edit - Remove

Peter

True words. Love you more than ever.

Posted by Peter on Friday, December 07, 2007 at 12:44
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Lisa Left Eye Loopylalalalala

Oh Moley, Moley, Moley. How do you keep reducing me to tears with just a few small words. Hang in there. Love to Mrs Moley too xxx

Posted by Lisa Left Eye Loopylalalalala on Saturday, December 08, 2007 at 00:29
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Caroline

CONGRATULATIONS Lisa on finishing the wretched chemo! Well done hun its time to celebrate!
It was so lovely meeting you at long long last on Monday - we didn't get much chance to have a natter, but at least I got to give you a hug. You look so amazing Lisa - your a very beautiful woman and your sure looking good and so well considering what your have been through! But then again, all of us are looking well! The inside is a different story, but we are all healing slowly but surely!
The Comedy Store night was a real tonic and I've not laughed so much in a long time - it was the laughter that boosted your little cells my friend - cos I think they boosted mine! Felt very energised on Tuesday! LOL xx

Posted by Caroline on Friday, December 07, 2007 at 12:45
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Umpalumpa

*Eyes leaking......*

I'm so proud of you Sis, you are amazing.


x

Posted by Umpalumpa on Saturday, December 08, 2007 at 00:18
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Bad Fish

I laughed (especially about the experience of marriage without the cost of divorce bit), I cried, I cried again and then I nodded a bit ... congratulations and yah boo to that nasty chemo. Hopefully you'll be tasting everything as it should be by Christmas and things will only get better. Hugs and more hugs to you and Becs!

Posted by Bad Fish on Monday, December 10, 2007 at 19:37
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suze

bless you loopy - this is a very moving piece of writing. Thank-you for sharing it this way,and I send all the love in the world for a brighter future for you and hope for all us "patients"
xxxxx

Posted by suze on Thursday, January 17, 2008 at 00:20
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Lisa Left Eye Loopylalalalala

I'm such a twit Suze, just found this waiting to be approved in my in box - doh.

And right back at you xxx

Posted by Lisa Left Eye Loopylalalalala on Thursday, January 17, 2008 at 00:29

2007 Nov 26th - Blood Test Rage....and Mobile Phones

Monday, November 26, 2007


The fifth element.................disappointment!
Category: Life

Harumpf!

Strangely I didn't bother washing my hair this morning, I thought, no I'll save the hair washing (with right arm in a plastic bag, it's such a chore) until Wednesday when I have my final chemo pump removed (pump number 15 in total) and PICC line. I had already planned to wear a new lovely purple shirt today which was a birthday present (thanks Angela ) because it looks great with the purple Accessorize bag I put the pump in (again thanks Angela!).

Having been awake (as is usual for me these days) until about 4 or 5 am I dozed off after waking at 8 and multipurpose life sized swiss army knife Becky was again my alarm call and chauffeur, not to mention chemo companion for the day. All was not good with Becky........but not for discussion here! Suffice to say with my lack of sleep we were both growling on her behalf by the time we arrived at the hospital after a quick shower.

It started well. A lady in a little car pipped and waved.............no we hadn't nicked her space (oh yeah I left my blue disabled park anywhere for free badge at home ) it was the red cross lady! She said not to hurry because there was no-one there to make us a cuppa, she was running late. Becky stayed outside to take a call and I strutted off in noisy heeled boots to the pathology dept. I checked my phone before turning it off (out of courtesy as they still have the out of date no mobile phone signs up) and was grinning at a text message. Tapped out a quick reply during which time some spineless jobsworth woman (a patient) remarked to her husband

"There's a sign over there".

Not sure why she was telling him because he wasn't using his mobile............. I told her

"Don't worry I'm turning it off in a second"

Obviously upset that I'd dared to respond to her talking about me whilst I could blatantly hear her, she offered this little gem:

"You shouldn't be using it at all".

Now as I'd had

a) very little sleep

b) very little patience with people who can't say something to my face

c) enough other concerns to reduce nosy parker tolerence levels today

I really couldn't be bothered to recite the following information, which I have been aware of for well over a year and having been an in and out patient at the hospital over the years I know how many doctors and nurses use mobiles in all parts of the hospital. I also know that they don't mind me using them when I've been in for treatment. This is not me playing the cancer card it's because of recent guideline changes reported in the British Medical Journal back in October 2006.

They write that the new, more relaxed, guidelines from the Medicines and Healthcare products Regulatory Agency (MHRA) are "less restrictive but still overcautious".

Dr Stuart Derbyshire of Birmingham University, UK, and Dr Adam Burgess of Kent University, UK, point out that patients, staff, and visitors often have their mobiles switched on, and there is no firm evidence of serious consequences.

The new MHRA guidelines state: "A total ban on mobile phones [in hospitals] is not needed and is impossible to enforce effectively" but "mobile phones should be switched off near critical care or life support equipment and should be used only in designated areas."

The guidelines add that ring tones and conversations may disturb patients, and that the use of camera phones may undermine patient privacy.

But the authors believe this could be more restrictive than the old regulations. They highlight the potential benefits of mobile phones over standard pagers, such as speeding up communication.

Interference with medical devices is rarely a problem, they say. In general, studies find it is "merely an irritation and ultimately harmless to the patient".

"We urge hospital managers and clinical directors to adopt a more flexible approach to the use of mobile phones on the basis that the advantages clearly outweigh their largely mythical risks," they conclude

Now I'm no technical genius but I didn't notice ANY critical care or life support systems in the waiting room for blood tests. It's on the ground floor right in a corner of the hospital away from anything else. Miles from Critical Care (I know I was in there in June).

Rather than attempt to explain this to the woman I just said

"I know what I can and can't do I come here often enough"

"So do I" was the witty retort...................

"If you have a problem why didn't you say it to my face instead of talking about me when you know I can hear you?"

"Oh SHUT UP!"

Hmmm................well there seemed to be no other choice than to tell her to

"Piss off".

I took my coat off and the sleeve that was covering my bloody PICC line and dressings in preparation for blood tests and line flushes - hoping she'd see it and think I was like really ill .............oh wait.........I am hahaha!

Becky came in a minute or two later so I warned her

"I hope you have turned your phone off because this "lady" will tell you off otherwise, she has a problem, an ATTITUDE problem"

Yes I know I wasn't exhibiting the best attitude myself, but seriously couldn't she have just said "Excuse me but I don't think you're supposed to use that in here, there's a sign on the wall". But no, she had to be rude about it so I'm afraid I snapped. I imagine she is rather like Blanche from Coronation Street spreading malicious gossip about all and sundry.

Anyway my blood test hurt and we trotted off to the chemo suite.

Neutraphils were 1.2........great. Had my line flushed and then went through my DLA claim form that had been sent to the hospital (received by them over a month ago but sent on 3rd October). It asked amazing questions like

Explain the condition and include whether it is mild, moderate or severe in your answer................Hmmm Stage 3b rectal cancer..........how bloody severe IS a life threatening disease. Bloody severe I'd say.

At least we got to use the phrase faecally incontinent again........loving that hahah!

So FIVE deferrals, refusals whatever you want to call them and now my trip to London is on the same day as my next chemo day. Also I had arranged to meet someone who was arranging travel details on the Tuesday. Faced with the dilemma of needing to finish chemo, meet friend AND attend London meeting without being affected by Oxali side effects. After debating my entire social life we decided I'll go to London, come back then have chemo at 9am on Tuesday and meet my friend there...........bit weird but well I'll be sat in a chair for a few hours and we just want to meet for a chat. Plus we get free tea from the lovely red cross lady! Sorted.

To compensate for our joint crappy day (two other chaps had rubbish blood and were sent home too, we were all pretty downhearted) we went off for a spot of shopping and lunch at the local department store for a whinge fest. It was great. Washed it all down with a cappuccino.

17:48 - 8 Comments - 4 Kudos - Add Comment - Edit - Remove

Caroline

Hmmmmmm Lisa - you have had a bad day - s**t! You could have done without that awful woman - that's all we need when we're feeling crap! Good for you speaking out - it has to be done sometimes cos peeps like that should just keep quiet!!! I had a rather nasty incident on the bus a couple of weeks ago with a senior citizen calling me all the names under the sun cos he wanted the window seat - he didn't say this - just told me to MOVE!!! I should blog on MySpace, but wouldn't be able to type what actually got said!!!! How dare he and also how dare "Blanche"!!!!
So looking forward to seeing you next week and I hope that the next few days are good ones for you babes cos you certainly deserve it. xx

Posted by Caroline on Tuesday, November 27, 2007 at 00:58
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Lisa Left Eye Loopylalalalala

Well Caz it was a tense day, it was never really likely I'd get the drugs as I scraped through last time with just .01 over the threshold. Nice bus passenger! And they say young people are rude? Still the bonus of no chemo is I'll be looking much better until I see you all and start blubbing! I'm actually feeling rather good overall, just nervous energy today I think and my little umpa has had much worse time lately so I was feeling aggressive on her behalf too, I think. See you in a week xxx

Posted by Lisa Left Eye Loopylalalalala on Tuesday, November 27, 2007 at 01:04
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Bad Fish

I'll send you some virtual pins to stick in the eyes of old bags who feel it's necessary to be jobsworths and whinging bitches!

I nearly got into a fight with some bean-headed little chav at the weekend (called him 'pottymouth' in front of his friends, which they thought was hilarious) and my Good Fish said afterwards 'don't worry - if he'd tried anything, I'd have lumped him'. Bless.

Posted by Bad Fish on Tuesday, November 27, 2007 at 00:58
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Lisa Left Eye Loopylalalalala

Haha I love that expression......it's one I'm quite familiar with as I can be one when riled.

I've done a lot of fishing myself lately and got a few in the net.......not decided which ones to set free and which one to take home for dinner!

Posted by Lisa Left Eye Loopylalalalala on Tuesday, November 27, 2007 at 01:06
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Peter

Oh dear, it must be something to do with the chemo(?)

Mrs. M was feeling stressed and took a day off last week so we went for a nice lunch together. A popular resturant, we waited for a table which was fine. Having ordered our food and bottle of wine, this "lady" with two very young children in tow ignored the queue for tables and said "you've got a table for four so we'll join you". So, in the best chemo tradition I replyed that, no, she wouldn't.

I wont bore you with the rest but neither Jackie nor I had wanted me to go into one but I did anyway!

Posted by Peter on Wednesday, November 28, 2007 at 01:09
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Lisa Left Eye Loopylalalalala

Hmmm now she's obviously rubbish at maths that woman if she thinks three adults plus two kids equals four anyway! I hope she was suitably embarrassed and you enjoyed your meal in peace after that, but I'm guessing she didn't have the courtesy to be embarrassed with such a lack of manners!

Poor Mrs M :o(
Poor us getting no evil chemo :o(

Still at least it was a bit warmer today...............my fingers didn't hurt once!

Posted by Lisa Left Eye Loopylalalalala on Wednesday, November 28, 2007 at 01:13
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GlitterGirl....

How funny that we're all discovering our confrontational sides...! Had huge fight with dippy neighbour who decided she was entitled to block the access road whilst using the cash point (slowly!)....her response? "But I live here...!"

I have never called anyone a "f*&king halfwit" to their face before. But it felt surprisingly good.

And don't get me started on the scrote who drove into the back of my car at the M6 toll booth on Friday....

Posted by GlitterGirl.... on Tuesday, December 04, 2007 at 20:28
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Lisa Left Eye Loopylalalalala

Fuckwit is Beckie's favourite cuss word lately, she was gutted one of the comedians used it ....she shouted "that's my word!" but not too loudly thankfully.........

Posted by Lisa Left Eye Loopylalalalala on Wednesday, December 05, 2007 at 00:48

2007 Nov 17th - Chemo Round 2 No 7

Saturday, November 17, 2007


What a slacker..........
Category: Life

Oh I say, I've been really lazy about this blogging malarky haven't I?

I think Santa may have got my note because despite my neutraphil count being only 1.3 on the Friday they somehow got up to 1.6 on the Monday!! Woohoo! Chemo number 7 full steam ahead. However I was desperately tired having been awake from 3.30pm on the Sunday and just wanted to sleep. Tough luck. I managed to sit myself next to a poor old chap who had enjoyed good health his entire life only to end up with leukaemia and then have a stroke mid treatment. To be fair apart from the fogginess and memory loss he was doing really well, no paralysis or speech trouble, unlike one of my bowel cancer buddues who had a stroke on the operating table, then got lung problems on top of being stage 4 and was looking pretty grim for a while. (If you or Sandra are reading this Dave, a big High Five for hanging in there and coming out the other side). He was in a total fog and asked me the same questions about 6 times. It's not an easy thing to reassure someone in a worse state than you when you are on the verge of madness through lack of sleep. Every time I closed my eyes to try and doze, he asked me again, "How often do I come here love?".

Tuesday I saw my lovely surgeon (now by lovely I do not mean the marrying kind, he's just a bloody good surgeon and he saved my life). More agonising examinations......grr I wish I didn't know how big those rigid sigmoidoscopes are.......just the thought of it makes me clench. He couldn't see enough due to the pain (and my cries of OW were probably putting him off) so is going to do a flexible sigmoidoscopy under sedation in the new year. I have had one without sedation but given my radiation damage it's too painful now. Of course given that my sisters seem to be immune to sedation I'm not looking forward to that either!

If everything looks OK and has healed properly then I should get my reversal sometime from March onwards. Five days in hospital and then about 3 weeks in the toilet (must redecorate them both as a priority) and oh bugger - I get my body AND my life back.........

What the hell am I going to do then?

Well firstly I'm going to have to start applying for jobs closer to home now. I need to find an employer who doesn't mind the fact that I'm going off sick for four weeks minimum in March............end of the financial year.......hmmm. Busy period for most businesses. Of course you'd think I'd consider going back to my current job - firstly no-one has bothered to tell me what the hell I can do IF I go back. My seconded job has ended, my desk no longer exists. My job prior to secondment a year ago has been subject to re-organisation and no longer exists. Add to that, I haven't been there since February and have probably forgotten how to use our systems. Oh and the thought of driving for an hour each way with an unpredictable rear end doesn't fill me with excitement. My best friend, both at work and outside work is out in the field following promotion and a lot of good people have been made redundant or left in my absence. I'd love to be made redundant. Just this one time.

I've done the trekking down to London to hot desk down Shaftesbury Avenue at Performance offices where you can just plug your ipod into the sound system that filters music into to the office all day. I've done being out of the house for 13 hours just to complete a 7.5 hour working day and frankly it sucks. I spent 7 years working my way around the company to get a job I loved, was good at and wasn't phased by meetings with directors because they knew me by name. My half pay is probably all I'd get locally for doing a full working week! But it's all relative. I've been working since I was 14 (part time then obviously) apart from the 5 years I took off to be with my babies. Thanks to insurance my mortgage is now much smaller so I can afford a drop in income. This is the first year I've ever claimed Tax Credits and am frankly stunned that I qualified on what I thought was a bloody good salary for additional pay outs.

I just want something easy with a small friendly firm, close to home or schools which covers the mortgage, the bills, fuel and food with a little left over. Which is exactly where I was before but I had a bigger mortgage! Weird thing is, now I know I'll still get tax credits to top me up to over the income I was earning before..........so I feel guilty if I accept them because I've always managed without benefits since I was 18. Then I think about the hoardes who never bother to work at all. I think about the hard graft I've put in working 7 days a week, or 5 days and one night shift a week (I'm practised at staying awake for over 30 hours at a time and still feeding children, doing laundry etc). I think about all the prescription charges I paid for when I was entitled to an exemption and I think SOD IT. I got cancer, I dragged myself through it with a lot of help mostly from my little Umpalumpa and three very good friends (Angela, Hayley and Mike). I've earned the right to take what's on offer for the next year or two aren't I? More importantly my children have earned the right to see their mother recovering and NOT being away from home. The thought that I may now be able to take them to school, fetch them home with a bit of work in the middle is keeping me going. Once I've got some energy back and am not bedridden by lethargy, pain and side effects. Next year is suddenly looking a hell of a lot better.

Meantime, I've got to jab myself in the belly with the GCSF - little soldier cells just have to fight their way through to 26th November so I can have a party on the 28th when hopefully the 53cm spaghetti will get ripped out of my arm!

WOO.....AND INDEED....HOO!

Please keep them crossed people xxxx

13:49 - 4 Comments - 4 Kudos - Add Comment - Edit - Remove

Mandy

Great to hear from you Lisa,

Having a laugh at the thought of you re-decorating the toilet and the hospital though (sorry)!

Fingers crossed the next chemo runs to time, I know how good it feels to finish before Christmas, as that's what happened to me last year.

Take care
Mandy x

Posted by Mandy on Sunday, November 18, 2007 at 22:47
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Peter

They're all crossed for you.

Posted by Peter on Sunday, November 18, 2007 at 22:47
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Bad Fish

I sympathise with the work thing - I can't bear the thought of going back to work in London - 3 hour daily commute - and not having been there since February either, I'm not sure what I'll be facing. Some of my friends have left too ...

Got an e-mail from one of my bosses yesterday evening asking when I was coming back. Er - next year do?

I was laughing at Peter Hain's interview on the Today programme this morning about Inacapacity Benefit: 'it's not what people can't do, it's what they can do. Can they sit in front of a TV screen, sorry, PC with a mouse'. Well Pete I can, but I can't type properly, I can't grip competently either (so no lifting) and I don't want to travel for an hour and a half with a bunch of morons on a train to not do it.

Posted by Bad Fish on Tuesday, November 20, 2007 at 17:53
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Umpalumpa

Fingies and toes crossed, champagne on ice xxxxxxxxxxxxxxxxxxxxxxxx

Posted by Umpalumpa on Tuesday, November 20, 2007 at 17:53