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Posts Tagged ‘chemo’

A bit of a setback?

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I went to see my surgeon, Mr Robert Carpenter, on Friday. It was the first time I’d seen him since my initial diagnosis, since when he’d left me in the capable hands of oncologist Dr Alison Jones. It was time for a check on my progress and to have a bit more of a discussion about my surgery.

I was not really expecting to hear anything that I did not already know. I have been having consultations with Dr Jones every two weeks and all seemed to be going to plan. Pieced together from the initial conversations I’d had with Mr Carpenter, I had begun to think, or rather hope, that he would be able to perform a double mastectomy plus reconstruction all in one operation. That operation, I thought, would be done about three weeks after I finished chemo, therefore toward the end of April.

I must admit I wasn’t sure whether all that, plus the removal of lymph nodes, could or would actually be done in a single operation. But I could hope. Yesterday though, after examining me, Mr Carpenter declared himself unhappy with the condition of the skin on the affected breast. There was an oedema, fluid under the skin, that he was not happy with. If this does not improve significantly with the next couple of treatments, he will not be happy to do a reconstruction at the same time as the mastectomy since he would have to use my own skin in the rebuild.

His suggestion therefore was that he’d do a single mastectomy plus the lymph node removal in April and then wait three months before removing the other breast and doing the reconstruction. I must admit my initial reaction was disappointment. That would mean at least July before the big stuff was over. Martin was with me and I think he was equally concerned.

The removal of the right breast is a decision Mr C appears to want to leave up to me. It is, after all, a preventative measure. When he originally talked to me about it though, he explained that since they believe my cancer was caused by the radiotherapy I had at 18, both breasts would have been equally exposed to the radiation and therefore both were equally at risk. I can’t therefore see that I have much choice and anyway, from an aesthetic point of view, I’d have thought I’d be better off with a matching pair!!

Before leaving 145 Harley Street I had to go in to Mr C’s secretary to book a follow up appointment with him after my next two treatments. She also pencilled us in for the first operation on 20th April. That brought it home. We left in silence. Then Martin pointed out that in the scheme of things two or three months was nothing. There were more important things to worry about, like getting through this. He was right, and anyway, we were never sure it would be only one operation.

I walked him to the taxi and returned to number 95 Harley Street, the Leaders in Oncology Care (LOC) clinic where I have the chemo, to have a blood test. I think Dr Jones needed to check my blood count after I’d started the second drug, Taxol.

Luckily, the girl who did my blood test was good and managed to get my vein first time. I was not in the mood for being prodded and poked. I needed cheering up and luckily my old friend Lesley, who lives not far away in Camden, had offered to meet me after my appointments.

I made my way to Marylebone High Street and to my favourite little cafe for a coffee and some toast. From there I texted Lesley and we agreed to meet in another cafe/deil, Natural Kitchen, just acros the road from where I was.

I’ve known Lesley since we lived next door each other as young children and although we have seen very little of each other over our adult life, it was so easy to talk to her and very therapeutic. We had a drink and a long chat. While we were nattering I spotted Martha Lane Fox come in. Martha was co-founder of lastminute.com. I met her and co-founder Brent Hoberman before lastminute was well known and was highly impressed with their professionalism, enthusiasm and belief in themselves. I joined Citywire in February 2000, about six weeks before lastminute floated on the stock market at a hugely inflated price that even Martha and Brent thought was ridiculous and followed the incredible hooha surrounding the flotation, which marked the beginning of the end of the dotcom boom.

Despite the subsequent dotcom crash, I always stuck with lastminute, recommending the shares because I knew Martha and Brent were more than five-minute wonders. Sadly, Martha had a very serious car crash, or rather jeep crash during a holiday in Morocco in 2004 and she still walks with a stick and looked pretty frail the other day. It hasn’t stopped her having a busy and I’m sure fulfilling life and this won’t stop me either!

After lunch with Lesley in Carluccio’s, I headed home. I was trying to focus on work and really wanted to get a story out, but I may have been a bit hard on myself. I had a lot to take in and frankly I just couldn’t concentrate on the story I was hoping to work on. In the end I gave up and met up with Martin and friends John and Ross for a pre-dinner drink at Camino’s on the river. We then had a pleasant dinner at friends Dawn and Martin, where were joined by four other neighbours and friends.

I’m glad that I am seeing my oncologist, Dr Alison Jones, on Tuesday before my next chemo session. I need to talk this latest development through with her. I suspect her take on it will be less negative than the impression I got from Mr C. We’ll see.

In the meantime I enjoyed the weekend down in Ramsgate, spending time with stepson Mat, daughter-in-law Claire and granddaughter Olivia on Saturday — a real tonic– and enjoying a nice meal with friends at Age & Sons on Saturday evening. The sun was shining, spring was in the air, and all will be well!

Never mind the chemo, thank goodness for the gym!

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I have to admit I was feeling ratty. We had a fairly quiet weekend, during which I did feel a bit tired, but then the less you do, the more likely you are to feel lethargic, regardless of whether you happen to be undergoing treatment for breast cancer or not.

On Saturday, Martin decided to go out to work for a few hours. This left me deciding what I wanted to do with my day. I considered going to the cinema to see The Artist, but the first showing of it at our local cinema wasn’t till 3.30. I’ll pop out for a walk down to Canary Wharf, I thought, but that really didn’t inspire me. I suddenly realised that I didn’t actually want to do anything. Sometimes it’s hard for me to admit that, but I opted for sitting down and watching a couple of TV programmes that I’d recorded.

It was a good decision. Nothing wrong with curling up in front of the TV occasionally. As I’ve said before, it is still February, and that always has an effect on my mood and energy levels. I remember many a year where I’ve wandered round the vitamins and supplements section in Boots looking for something that promised an energy boost. Considering I’m over half way through chemo this year I’m probably less tired than I’ve been on those occasions.

Friends Sue and Tommy were due back from their month-long holiday on Saturday and early afternoon they called to say they’d be popping over to Canary Wharf and did we want to meet up? That was just what I needed. I could enjoy the rest of my afternoon chill out with a little sortie to look forward to. As it turned out, Martin was finished by about 4.30 and we popped down to the Grapes. Sue and Tommy abandoned their shopping plans and came to join us and we all opted for an early meal in the local Italian, La Figa. We had a very pleasant few hours but it was uncharacteristic for all of us to be pleased to part and head home at just 8.30 on a Saturday night!

The sun made a welcome appearance on Sunday and we decided to venture out for a walk. Once again, I was not feeling 100 per cent at the start of the walk but the air and the exercise always make things better. We walked through Wapping and St Katharine Docks and then over Tower Bridge to Shad Thames, a good 50-minute walk. The breeze was a bit keen and I warmed up with a cappuccino in All Bar One on the river. The walk back was broken by a visit to Waitrose and a drink in the Captain Kidd. We were home by 4 and had a pleasantly quiet evening.

Bloated

Monday morning I was still feeling what I can only describe as ratty. The French have a good expression for it, which literally.translates as “I don’t feel good in my skin”. If I’m honest, I think it was mainly because I was feeling bloated. As someone who has always had to fight to keep my weight down, I’m still very affected by feeling that it might be creeping up.

That gives me an interesting dilemma at the moment. I remember getting on the scales not long after I started chemo and thinking that I had lost a couple of pounds. For the first time in my life I was suddenly worried about losing rather than gaining weight! While I was on the first lot of drugs, AC, I seemed to need to eat more to keep my energy up and seemed to be able to eat what I liked without affecting my weight. Martin commented that he’d never seen me with such a good appetite. I loved it. I was really enjoying my food, feeling that I really needed it to keep me healthy.

It’s incredible how quickly that feeling can change. I think it must have been when they weighed me before chemo on Tuesday. Of course I might have been wearing heavier clothes and everyone fluctuates slightly, but I think my weight was up about half a kilo. Yes, I know in old money we”re talking about a pound or so, but it was enough to pull me up and make me think I still had to be a bit careful. The steroid anti-sickness drugs I take for three days after treatment do seem to make me feel bloated, and this time I could have experienced stomach cramps, so bloating ought to have been the least of my problems. But it just added to be feeling not quite right “in my skin”.

I could probably have knocked it on the head on Monday by going to the gym, but my dad goes to art on Mondays and I wanted to take this rare opportunity to spend lunchtime with my mum. It’s not going to be possible once I’m back in the office so I just have to make the most of it while I’m working from home. In the middle of the day it takes no more than 15 minutes to drive over there. I knew she’d be keen to get out and that the dangerously local Westfield shopping centre was beckoning.

The ratty me was perhaps not the best companion, but mum did her bet not to notice. In truth, we didn’t really have anything to get, but we managed to manufacture a reason to be there. A coffee and a light lunch were in order and revived me. Weight concerns or not I still needed food. It was a pleasant interlude and as I said, a privilege to be able to spend quality time with elderly parents.

By the time I got home I was in a better mood and ready to get down to writing up my story for work.

On Tuesday there was only one thing for it, a good session at the gym, and it could not have come soon enough. I woke early and set about making an online application for a Criminal Records Bureau check for Martin, who has to complete one as part of re-applying for his taxi licence.

Tedious

As is my wont these days, I sat on my bed with my iPad and went through the tedious and lengthy process of the application, leaping up and down to find the documents — passport, driver’s licence, letter from a government department or utility bill — required. I got all the way to the end without disaster, until I was presented with a screen containing a letter complete with barcodes. Please print this out and take it to the Post Office to get your documents verified, it said. But I’m on my iPad, and as far as I know, I can’t print from the iPad. I panicked, and my sister chose just that moment to phone me!!

She’s not the most technologically friendly person and she doesn’t have an iPad but she thought she was being helpful by suggesting I might be able to save the form for later. Sadly, she took the brunt of Mrs Ratty”s rattiness. And luckily, friend John, aka tech support, was on hand to save the day. Take a screen shot of the letter and email it to yourself. Simple when you know how!

Knowing that I needed a serious dose of gym I’d decided to do the 30 minute abs class followed by Pilates. I knew the abs class was a tough one and I had some doubts as to whether I was up to it. Well, I’d give it a go. I could always stop, I have a pretty valid excuse!

The first five minutes, where he had us doing planks and press-ups in quick succession were excruciating. I even thought about stopping at one point and just waiting for Pilates. But for a start, it got a bit easier for a while and also, I looked around the room and realised that almost all of the men and women in the class were suffering too. Ten minutes in I was puffing away and feeling better than I had for a week! The class finished as it had started, with more of the really tough exercises, but I coped. Pilates was a welcome relief. Tough, but in a different way.

By the end of it all, Mrs Ratty had finally been banished. I just cannot stress enough how much better you feel when you make the effort to do some exercise. Chemo or no chemo we all have to push ourselves sometimes, but I can’t ever remember a time when I’ve regretted having been to the gym. So today, power yoga here I come! I feel good in my skin again. Thank goodness for the gym!

I don’t do side effects!

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I dutifully listened to the list of potential side effects from this latest chemo drug, Taxol, then parked it. I don’t do side effects! It’s all too easy to start imagining them but far better to tell yourself you’re just not going to have them and that’s that!

So far, so good. Since my treatment on Tuesday I’ve been pretty good. Not as tired as on the previous drug, AC, although even that wasn’t bad. And so far, no sign for the stomach or muscle cramps that I might have had. As I say, I don’t do side effects, my new mantra!

Not knowing what to expect this time round I didn’t make ambitious plans for the day after chemo, but my old school friend Franny came round for lunch and actually I felt fine. We had a good natter over a light lunch that I actually made myself! Anyone who knows me and knows that Martin does all the cooking thinks I’m actually incapable of preparing food. Not true but suits me to let them think it!

Thursday I decided to push myself out to the gym. Power yoga was a little challenging to start with but then it was six days since I’d done any exercise and it could have felt tough under any circumstances. As always I felt far better for having done it. Lunch with friend Gilly and a little tour of the Museum of London for a change before returning home a little tired to work. The girlfriends are really rallying round and time with them is much appreciated, especially since working from home could otherwise be quite isolating.

On Thursday evening we went over to mum and dad’s with Lou and Bev to celebrate dad’s 85th birthday! He’s doing pretty well considering but could well have done without having to worry about his eldest daughter yet again! A pleasant evening was had by all with plenty of laughter and giggling. It takes years off my mum when she starts giggling like a schoolgirl.

Friday morning went well work wise. I spotted a story nice and early and managed to interview the relevant parties before midday. It rarely works that smoothly. Another interview was carried out en route to meet yet another girlfriend, Dena, for lunch before she and husband Trevor left for the Caribbean the following day. We had a lovely healthy salad lunch and plenty of chatter at Rocket in Mayfair. The location, Lancashire Court, was a revelation to me. Never even knew it existed. It’s a little warren of alleyways with restaurants and boutiques just off New Bond Street. That’s London for you. Always places that surprise no matter how long you’ve lived there!

I headed back home on the riverboat and got down to writing up my story. In the evening we popped down to the local, The Grapes, for a pleasant hour or so, before eating another of Martin’s tasty and healthy dinners — salmon, rice and sun-dried tomatoes on this occasion.

We are having a rare weekend in London with no particular plans. Makes a change occasionally but I’m not good at doing nothing. Martin’s popped out to work for a few hours and I’m starting to twiddle my thumbs. Think I’ll have a wander down to Canary Wharf. It’s day five and I’m feeling good. I don’t do side effects!!!!!

Chemo day — a bit of a marathon!

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We had to be in Harley Street for 11am for my echocardiogram. I needed this to check my heart prior to starting a new drug, Taxol. Lou and Bev had unquestioningly offered to accompany me again and as my sister won’t use the tube they drove to me and arrived at 8.45. We got the river bus and then a bus up to Oxford Street and arrived in time to grab a coffee before my scan.

The scan took about 20 mins and the results were in my hands five minutes later. We then had and hour and a half before my appointment with my oncologist, Dr Alison Jones, so we headed to Marylebone High Street. The safest (financially) place for us there was the Oxfam bookshop, where we bought family birthday cards and had a good giggle at some very funny cards on display.

With time for an early lunch we went to the excellent Marco Polo cafe which offers delicious food at decidedly non-Marleybone High Street prices. I had a lovely avocado salad, Lou had falafel salad served with humous, tabbouleh and much more and Bev had a classic mushroom omelette.

Dr Jones was her usual charming self and seemed pleased again with my progress. We talked about me going to see my surgeon, Mr Robert Carpenter, soon, and I asked her for suggestions of worthy breast cancer charities I might support in future. One of her two lovely secretaries greeted me warmly, booked my next appointments and even phoned Mr Carpenter’s secretary for me to coordinate my appointment with him and a blood count test.

We then had a 40-minute wait for my scheduled chemo time at 2pm. We knew in advance that these next four sessions of chemo would take quite a bit longer than the first four. The Taxol takes about three hours to administer where the last lot took only an hour and a quarter. But a delay in getting my blood results did not help matters. I was told initially that the analysis machine at the clinic wasn’t working and the samples had to be sent round the corner. But I think there may also have been a query over one of my levels, which was a bit high.

It must have been at least 4pm before my lovely nurse Emma, who has looked after me for three sessions now, came and started my pre-meds and it was 5pm before the actual chemo started. Luckily, you really don’t notice the time pass when Lou’s around. We spend most of the time giggling (which belies her nervousness. She did not relax until my blood results were back, fearing there was a problem. She does the worrying so I don’t need to!).

About 1% of people get a bad reaction to Taxol. I realised that there was therefore a very low probability that I would, but it was still a bit of an anxious time waiting for the first 50ml to run through, by which time it was highly likely I’d be fine. Emma waited with me until I was in the clear and Lou stood glaring at me as if to say, “You definitely won’t have a reaction!” Whatever it was, it worked.

Apart from just chatting and giggling, we passed the time doing the Times jumbo crossword and at about 5.30 I had another wonderful 30-minute reflexology treatment while Lou and Bev popped out for some well-deserved fresh air. One member of staff commented on how infectious our laughter was and a visitor in the next booth came past when she was leaving and said how wonderful it was to see us all laughing and eating and chatting.

Lou and Bev are very organised. They’d come prepared with a little picnic, so we had chicken wings and miniature scotch eggs for sustenance and plenty of tea and coffee from the clinic to keep us going. Despite Emma’s very best efforts were were not ready to leave until 8pm. Martin stayed out working and was there to pick us up. He’d parked the cab a bit earlier and popped to Marylebone High Street, where he’d found the butcher still open. He bought some wonderful calves liver for our late Valentine’s dinner and a goodie bag of deli stuff for Lou and Bev, knowing they’d be even later home than we would.

We were all pretty tired after such a long day but relieved that all had gone so well. After a delicious dinner and a short rest I got to bed at 11pm, took a Nytol to counteract the steroids, and had a pretty peaceful night’s sleep. Onwards and upwards!!!

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Preparing for round two!

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I’m having a little battle with myself at the moment. Next week I start the next lot of four chemo treatments. The first four have gone really well considering. There is no real reason that the second four should not. But it’s a different drug (the first was AC and the next will be Taxol) and therefore a possibility of a different reaction to it. In another two weeks I will also start on Herceptin.

My oncologist, Dr Alison Jones, told me last time that she didn’t want to start two new drugs at the same time in case I had a bad reaction to one and she would not know which one it was. Perfectly logical and I know you can have a bad reaction to any drug, but most people don’t. So my main problem this week is to stop worrying about the vague possibility of a bad reaction. It’s all too easy in these situations to start imagining symptoms, which is the last thing I want to do. It really won’t be helpful. Have just spoken to sis about it and she’s been firm with me. “You’ll be fine,” she insists, and I’m sure she’s right.

This week has been a pretty normal one, well the new normal anyway. I’ve worked from home, been to the gym twice, and had two lunches. The first was with sister Lou and her ex-husband Hugh. That may seem odd to some, but they have remained good friends since they separated more than 20 years ago and I have kept in touch with Hugh too. He’d been living in the States for years with his American wife and they’re now in Edinburgh.

Hugh took the opportunity of coming south to see one of his sisters and an old friend to come to London and buy us lunch. We had a wonderful Tapas at Comino’s on Canary Riverside. Plenty of friendly banter and a very pleasant interlude.

Yesterday I met friend and near neighbour Jud for lunch at Plateau in Canary Wharf. She knew I was working from home and might need some company occasionally and kindly offered lunch. We had a very pleasant lunch and chat and reckon we’d put all the world’s problems to right by the time we’d finished.

Meanwhile, I’ve been I touch with both girlfriends who are also fighting breast cancer this week. The three of us were at secondary school together. Elaine was diagnosed last June and is coming toward the end of her treatment. Diana was diagnosed on,ya couple of weeks ago and had a lumpectomy this week. She has to wait a couple of weeks before she finds out what’s next but hopefully, as hers was caught very early, it won’t be chemo.

Scary though to think the three of us should be going through it at the same time! They made us tough at Wanstead High though and I’m sure we’ll all come through with flying colours!

Will make the most of the next three days despite the best efforts of the weather! Going to the gym to do abs and Pilates today and hopefully going down to Ramsgate tomorrow to see friends and catch up with all the grandchildren. Just hope the ice and snow behave.

It’s not chemo, it’s February!

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If I’m absolutely honest, this has not been my best week. It could of course have been far, far worse. But I have struggled a bit. Chemo on Monday went fine. That’s what really matters. Tuesday, as I’ve mentioned in a previous post, was a tired day spent at home. Wednesday and Thursday, I went to the gym, managed power yoga quite easily, popped into the office on Thursday afternoon, but it all felt a bit of a struggle. The weekend, while very pleasant, also felt a bit difficult at times. And then I realised, it’s not chemo, it’s February!!

I have had a problem with February long before I ever heard the phrase: “SAD syndrome”, or seasonally affected disorder. I can remember a February spent in Bordeaux when I was 21 and living there for the year as part of my French degree course. Bordeaux in Feb was grey, chilly and depressing. Only a skiing trip to the Pyrenees could alleviate the gloom, but coming back felt even worse.

Since those days I have always struggled. Each year I get through January relatively unscathed and think I’ve cracked it. Then suddenly, I’m feeling tired/ratty/fat/ugly, you name it. A few years ago it became so obvious that Martin insisted we book a holiday to the sun at this time of year. Two years ago we had a lovely week in Dahab, Egypt, on the Red Sea, learning to windsurf! The sunshine and exercise were a powerful tonic. Last year we treated ourselves to two weeks in Key West, Florida. We went out with our friend Jill, whose daughter lives there, and stayed on a boat for the two weeks while cycling around key West and generally chilling out in the sunshine.

This year, for obvious reasons, our plans of escape are on hold. I did not think I minded. Escaping for a week’s sunshine was the least of my worries. Besides, the, dare I use the word, “novelty” of my situation, the sheer adrenalin needed to cope with everything that has recently been thrown at me, seemed to have protected me from the ravages of a UK winter. Until this week, that is.

This weekend, we decided to go down to Poole, where Martin comes from, both for a break and to see our brother, sister-in-law, niece Kimberley and her one year-old son Harry. When we arrived on Friday, the sun was still shining. I worked in the car on the way down and when we arrived, leaving Martin to get us out of London before the Friday rush.

We headed for our favourite spot, The Haven Hotel, Sandbanks. We even managed to sit outside by the water for a while enjoying a dose of early February sunshine. Then a walk along Poole quay and we were feeling quite restored. But Saturday morning was cold and dull. I’d not had a great night but I was not the only one feeling tired and lethargic. The four of us ate breakfast, sat watching Saturday kitchen and generally couldn’t work up much enthusiasm for anything dynamic. Eventually, Mary decided she needed not pop down to the local Tesco and we all realised that perhaps a little walk would do us good.

Fortunately, once clad in our many layers, Martin suggested that since we were out, why not have a longer walk? So we set off for Poole Park, Baiter and the quay. For the first 20 minutes or so I felt peculiar. It was a strange, spaced-out kind of feeling that I remember having after the first chemo session but not really since. The air and the exercise though were just what I needed. Gradually, the odd, foggy feeling started to lift. We stopped off on the quay for a drink and then made our way home. We must have been out for at least two hours and everyone felt better for it.

Kimberley and Harry were there by the time we returned and we all had a pleasant afternoon eating lunch and chatting. Foiled by the weather again though, we decided to stay in for the evening, when we ate some more and watched TV. It did not help any of us with our feelings of lethargy and my 10pm I was ready for bed.

On Sunday morning, Kimberley came to the rescue like a little angel. She is a beauty therapist working in a Clarins salon, and she offered to give me a facial. I’m pretty sure I’ve only ever had one once before and that must have been years ago. While Martin and Paul took Harry out for a walk and Mary busied herself with tidying up after us all, I was treated to a most wonderful hour of facial and massage. Not only is Kimberley highly qualified, she has a really wonderful touch. Even more importantly, she had so generously offered her time and expertise to her aunt at a time when she needed it most. By the end of the hour I felt better than I had done all week. What a wonderful gift!

Martin had suggested extending our weekend away by stopping for the night in a hotel on the way back. We considered trying a boutique hotel in Sussex that had been recommended to us. But frankly, I think it would have been wasted. The combination of the weather (London has had its share of snow) and that February feeling meant that what I really wanted to do was just get home.

We may consider going somewhere different next weekend. My next chemo is not until Tuesday 14th. By next weekend the drugs will be out of my system and I should be feeling much more “normal”. But it will still be February when all’s said and done and I must remember that. Don’t blame the chemo, it’s doing just what it’s supposed to do. And so is February. Just hang on in there. The days are getting lighter after all!!!!

Four down, four to go

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Had my fourth chemo session on Monday. That was the last of the drug AC. The next four will be a different drug, Paclitaxel, or Taxol. So far, so good. I’ve had the odd day of feeling a bit tired, but nothing drastic. This week, Tuesday, the day after chemo, I did feel quite sleepy. It was very cold and dull out and I allowed myself a day in doing very little. Mum and dad had offered to come up to see me and we nearly changed the plan because I was tired. But while they are both still capable of getting on public transport and coming under their own steam, I didn’t want to miss the opportunity. They came for a couple of hours and it was great to have them here.

My mum was due to have come with me to chemo on Monday but unfortunately had been in agony over the weekend with what appeared to be a trapped nerve in her shoulder. It must have been bad for her to suggest not coming. On Sunday we went round to mum and dad and Martin cooked us all lunch. Lou and Bev popped in for a while too. Family time is extra special these days!

The chemo sessions are not in any way scary. Everyone who works at the clinic is lovely and friendly and having the port in makes the whole process from taking blood to administering the chemo so simple and painless. Half the time there is spent waiting for the blood results and the waiting for an anti-sickness drug to kick in, which takes an hour. So having company is not essential, but it is undoubtedly pleasurable and helps pass the time. My sister Lou has been with me every time until this week and has insisted that if no one else is coming, she will. This week friend Gilly was available and very kindly offered to come with. We met at Harley Street at 1.30 although I wasn’t called down until 2. We spent an hour and a half drinking coffee and chatting until Gilly had to leave to get over to Holborn for an acting class she’s signed up for.

No sooner had she left than my reflexologist turned up for my 30 min session. Lovely! At one point I was lying back in my reclining chair with the reflexologist gently working my feet and my lovely nurse Emma administering the chemo. One could get used to being waited on like that — well perhaps not, but it does ease what might otherwise be a daunting experience.

Yesterday, two days after treatment, I’ll admit feeling a tiny tad nauseous when I woke up. It’s probably the first time since I started the chemo and it was only mild. I forced myself to eat some porridge for breakfast and then decided that some fresh air would do me good. It was a cold but sunny morning so I wrapped up in several layers including a scarf and sheepskin hat for my head.

My plan was to pop down to the post office collection office to collect whatever it was that someone had sent me with underpaid postage and then see how I felt. I had in mind to go to yoga if I felt up to it so took my gym kit with me. In the event the cold sunny air did me good. I have found throughout this that getting out for a walk however tired or wooly you feel is the best cure.

I paid the £1.36 charge to collect the letter that one of my specialist’s secretaries must have forgotten to frank or stamp! £1 of that is Royal Mail’s “handling charge”. I should charge them a handling charge for all the undelivered mail I never receive!

I headed for the Docklands Light Railway and went to the gym for a 45-minute power yoga class. Like walking, you always feel better for doing a class. I didn’t want to overdo things though so walked back along the river to Tower Pier, still in glorious sunshine, and took the river boat home.

Refreshed from my walk and yoga I was able to get down to writing up an article for work, which also made me feel better. I then sat and watched the film “Miss Pettigrew Lives for a Day”, which was sweet but did not do justice to the book, which I’ve recently read.

Shortly after Martin came home I went into the bathroom and, washing my hands and looking in the mirror, I had a moment. I’d read about women going through chemo who said they just wanted themselves back. So far I’ve really had no problem with my hair loss or with the mild side effects I’ve had so far. But for just a second, looking at my little bald head in the mirror, I did think I wanted me back. Then I realised I haven’t gone anywhere!!

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It must have been a shock?

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I met a friend at a party on Saturday who I hadn’t seen for a few months. Barbara used to be the landlady of our local pub, the Grapes, and moved back to her flat on the other side of town in September when she sold the lease to Grapes neighbour Sir Ian Mckellan and his partners in the venture, theatre director Sean Matthias and Evening Standard owner Evgeny Lebedev.

Barbara didn’t know about my breast cancer and she was quite shocked and sorry to hear about it when we met. In the cold light of the following day she emailed me, reiterating how sorry she was. “It must have been such a shock,” she said. I thought about that. My girlfriend who was diagnosed last week and who has been caught very early, broke down I tears when I spoke to her. “I’m really sorry,” she said, knowing that in the scheme of things hers was considerably less serious than mine, “It’s just that I only found out a few days ago and it was such a shock,” she said by way of justifying the tears.

Had it been a shock to me? I wasn’t even sure. On one level, it must of course have been. The only things that would have mitigated that shock were the fact that I knew there was something wrong myself, and I suppose the initial shock came when I got a recall from my mammogram, confirming my own worst fears.

I know it was a huge shock to Martin when I came out of the first consultation with the specialist, lent into the cab on my way across the road to see the secretary about booking all my tests and told him: “I’m afraid he’s pretty sure it’s the big C.” But from that moment, I went into overdrive.

When Martin asked if I still wanted to go down to Ramsgate for a party that weekend, I said, of course. We had to carry on as normal until something stopped us carrying on as normal. And that it precisely what I have done so far. In the nine weeks since that day I have carried on as normally as possible. I am actually having my fourth chemo session as I write this. I suppose there have been moments when the “shock” did start to filter through. But not many. Which led me to consider, when Barbara suggested it must have been such a shock, whether in fact I was still ‘in’ shock.

Ironically, we have just watched the film “The Bucket List” with Jack Nicholson and Morgan Freeman about two terminally ill men who write a list of things they want to do before they kick the bucket (I am home now after chemo, which all went well and to which I was accompanied by my friend Gilly, thanks G, and once she left I had a lovely reflexolgy treatment).

The film had some pretty awful reviews when it cam out, ( see this one for example, http://www.telegraph.co.uk/culture/film/3671168/Film-reviews-The-Bucket-List.html) but I thought it was excellent, if a little poignant in my situation. I mean, Jack Nicholson and Morgan Freeman. They could read the telephone directory and it would be fantastic. Anyway, whatever its merits, when they first found out about their illnesses they talked about the five stages of grief — denial, anger, bargaining, depression and acceptance. I thought, am I in denial? But I don’t think so. I had Hodgkins Disease at 17. It happened, I dealt with it, I got through it.

The same will happen this time. But that’s not to say I sit around dwelling on the idea of having cancer. I’m too busy communicating with and seeing friends and loved ones, keeping fit, working, oh yes, and having treatment and getting healthy.

So yes, it was certainly a shock for Martin and my parents and sister and all my family and friends. And I suppose it must have been a shock for me. But shock is not a productive state to be in. I have far too much to do in the next six months or so to entertain it. When I’m successfully through it all, it may creep up to hit me. But not now.

Difficulties to face? Ask the universe

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There was a time in my late twenties and early thirties when I got quite into “New Age” thinking; getting in touch with the universe, om.

I haven’t totally dismissed it all and at the moment I can certainly say that I must in some way be putting out my needs to the universe and the universe is answering those needs.

When I first met my breast surgeon, Robert Carpenter, two months ago, it was for my diagnosis. On that occasion, before any tests and confirmation that it was indeed cancer, he had already said words like “cosmetic” and “reconstruction”. But he knew I was not ready to take all that in and he knew that I had a whole lot of stuff to get through and cope with before I even started to think about surgery and its implications.

Now that I’m approaching the half-way mark in my chemo treatment, I have been able to start thinking about the next step, which will almost certainly be double mastectomy and, hopefully, reconstruction. This is a big deal. And I do know big deals when I see them. I had a hysterectomy at 44 having tried and failed to have children. Luckily I was ready for it and did not suffer any of the emotional trauma you might expect to be associated with it. I think it gave me closure. No children, move on (happily to my stepchildren and lovely grandchildren).

Having internal organs removed is one thing. Trust me, I’m the expert. I have no spleen, no thyroid and no womb or ovaries. But when I walk into a room, no one would ever know that. The mastectomy is something else again. Anyone who knows me knows I have a well-endowed bust. It is not something you can miss, particularly on my otherwise small frame. Those who have never had a proper bra fitting, take note. I wear a 30 FF. 30, because I have a very small back. FF, because, well you see what I mean.

I have had a love/hate relationship with this part of my anatomy. When I was in my late teens and early twenties, the fashion was all unisex. The flat chest was celebrated. I was born at the wrong time. I missed the voluptuous 1950s and by the 1990s and beyond, when girls started flaunting what they had and cosmetically augmenting what they didn’t, I was no longer young enough to do the same.

But having them removed is not going to be easy. I could not quite get my head round what it would be like. Which is when the universe stepped in and sent someone to help.

Saturday evening. I’d just arrived at the yacht club in Ramsgate for a 60th birthday do and was out in the hallway having taken my coat off. A couple I knew on what I would call a nodding acquaintance basis arrived. He sails in the races we take part in but not even in our class. They are often in the club and attend many of the functions and parties. But we have barely exchanged more than a hello. So I was quite surprised but very touched when he touched my arm and told me how sorry he was to hear my news. He had got my phone number and been intending to phone me, he said. Really? And then I realised why. She has recently been through the same thing, with a single mastectomy last year and recent reconstruction.

What happened next though was amazing. Looking stunning in her party attire and without any awkwardness or embarrassment, she invited me to pop upstairs into the ladies and have a look at her reconstruction. She had been able to see the results of a friend’s reconstruction before deciding to have her own, she said, and she was offering me the same opportunity. Surgery these days is amazing. Although recent, her scars were so neat, and the whole experience was greatly reassuring. Thank you so much! I will not name you but you know who you are. And thank you universe!! At just the time when I was starting to face such a big issue, someone I could not even have imagined turned up with the most amazingly generous gift, reassurance.

The fog lifts and the wigs arrive!!

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Before I had my first treatment, the nurse said he’d heard the post-chemo period was a bit like a hangover — you feel a bit grotty for two or three days and the you wake up one morning and realise it’s gone. I’d say that’s quite accurate, although the timing varies and also, I have to admit I’ve had worse hangovers in my time.

This week, following my third chemo session on Friday 13th (yes, lucky for some; they put me in pod 13 too!!) I was not bad at all at the weekend, tired on Monday and Tuesday and I wouldn’t say I had that post-hangover moment until Friday. But when it comes, you know it. You suddenly feel clear of drugs and as normal as you’re going to get at this time. I was determined to make the most of this feeling, particularly by going to the gym.

So I got blogging early, started work and made sure I would be ready to leave the house by 12. At 9.30, a parcel arrived via Royal Mail. At 10.20, another arrived, via City Link. They were duplicates, both containing two wigs. Having tried on wigs at Trendco in Notting Hill a couple of weeks ago, I ordered two online, knowing I could send them back if I, or more likely
Martin, didn’t like them.

They were due to arrive last Monday. By Wednesday, when I’d been in touch with Trendco and tracked the order online, City Link was claiming to have tried to deliver twice and left me a card. I felt compelled to tweet, asking them whether lying was all part of their service?

Not Trendco’s fault and we all know that when Royal Mail drops a card through your door saying they tried to deliver they rarely even have the parcel with them ((Lou caught her postman red handed recently). However, it was up to Trendco to sort out. They duly arranged both for City Link to deliver before 10.30am on Friday and for Royal Mail special delivery to bring another lot by 1pm, in case the phantom City Link driver failed to materialise yet again.

So by 10.30 I had four wigs in my possession. I duly opened the first two and tried them on. Oh dear. Not sure what I was thinking in the shop, but I really didn’t like the now! My sister-in-law Mary phoned. Wear one for a while and give yourself a chance to get used to it, she advised. I persevered for about ten minutes before giving up. It looked like a wig and felt like a wig. If I wasn’t happy, Martin certainly wouldn’t be. As I write, I have not yet even had time to show him, but I’m pretty sure that after all the hassle of getting them, sending all four back will be easier.

I had a quick shower and threw my gym clothes on. Took the DLR to the gym and arrived in time to take my time getting ready for class. I’d decided I could cope with a 30 minute abs class at 12.45 followed by 45 minutes of Pilates, and I was right — no problem. While getting ready, a woman came in and started changing next to me. She was huffing and puffing and cursed a key that she couldn’t turn in the locker and some other equally trivial disaster. I’m sure I’ve had times when I’ve done the same, got wound up over nothing. I wanted to point out to her that there were far more serious problems that could befall her. But instead I simply removed my headscarf and walked around bald for a while before putting on the little “yoga hat” I bought at Trendco. I don’t know if she noticed, but I hope it might have made her stop and think.

Two classes made me feel much better but were sufficient. Other than popping into House of Fraser on the way to the station to check out the scarves and hats (didn’t buy any!!), I headed straight home. I was ready for some lunch and a sit down. Did some work, popped down to the local for an hour, had dinner, watched Source Code on DVD (not really worth the effort) and had a early night in preparation for a fairly early start today.