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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.

Different ways of handling it — emotional space

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Yesterday I found out that a close friend of mine has just been diagnosed with breast cancer. She is still in the sort of shock that I realise I didn’t really go through when I got my diagnosis two months ago. There are a couple of reasons for that. Firstly, I spotted something wrong myself (a change in the shape of my left breast) and I instigated having a mammogram. So when I got a recall I was horrified but not shocked. Secondly, as my surgeon Robert Carpenter said to me on our first meeting, I have been through it before.

Yes, I do remember walking around in a daze for the first couple of days after my Hodgkins’ Disease diagnosis at 17. I was just about to start my A Levels. I remember sitting in my first French exam thinking “what’s the point? I won’t be around to get the results.” Fortunately, that feeling was very short-lived and never returned. What was I thinking of? Of course I’d be around. Now, where was the next party to go to?

Thirty-four years later, I skipped the first train of thought and went straight on to the “where is the next party bit. I had my initial consultation with Mr Carpenter on a Friday evening. Did I still want to go down to Ramsgate that weekend? Martin asked. “You bet”, I replied. There were grandchildren to see and a party to go to. “We must carry on as usual until we can’t,” I told him.

My friend, who doesn’t want to be named, has never been through it before. She is very shocked and upset. I would not want to trivialise her shock at being told she has breast cancer. But relative to me, she is a lucky lady. Hers was caught extremely early through a routine mammogram. The doctor told her she was one of their “scan successes” because what the scan picked up was so small she was unlikely to have noticed anything herself for at least a year. I, sadly, was one of the scan failures. I had been on annual mammograms on a higher risk list and mine was not spotted.

I actually shed some tears when I thought about that. I should have been like my friend, caught early. But then I decided that due to mine almost certainly being caused by my previous radiotherapy, the outcome might not have been all that different whenever they detected mine.

The other reason why I’m sure my friend has been less able to cope with her bad news than I was, is that she didn’t have any emotional space left. She has been dangerously stressed for the past year with her job, which is putting ridiculous demands on her, and with coping with elderly and infirm parents. I’ve been worried that she was pushing herself too close to the edge for some time, so the cancer diagnosis must have seemed like the final straw! I, by contrast, was, at the point of diagnosis, in a very good place. Things were going well at work and at home. My parents are elderly but still quite independent. I was physically fit and healthy. I had the emotional space to cope with this.

Naturally, I phoned my friend and had a long chat. Part of her obviously knows that she’s lucky hers has been caught so early. She is scheduled to have a lumpectomy and probably two or three weeks of radiotherapy after that. But I urged her to take this as a warning. No one can take so much sustained stress without consequences. Her job, while on paper a rewarding one, is clearly not serving or rewarding her in any way now. The demands being made of her are impossible to fulfil and she is getting the opposite of thanks for all her efforts. She really, seriously needs to use this nasty shock as a positive opportunity to reevaluate. I hope she will.

Going bald is easy!!!

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It’s weird how not weird this feels, after 52 years of having A head full of hair, to suddenly have almost none. I was even born with a shock of dark brown hair, so I’m told. Having taken the plunge and had my curls all chopped off on Tuesday, what little was left has continued to  come out prolifically, so much so that when I looked at the bath I’d just got out of yesterday I expected to look in the mirror and find I was totally bald. Yet still some hair clings on defiantly, probably to be finally conquered by Martin and his beard trimmer!

I have to return at this point to my experience at the hairdresser on Tuesday.  Fiona, owner of the John Harding hairdresser in St Katharine Dock, E1, was sweetly listening to me babbling away about what was happening to me and what I’d done since she last cut my hair probably more than 15 years ago. I suppose I thought I wanted to show that I was not traumatised  by having all my hair cut off and was being as chirpy as could be.

It was only when I happened to say that having been diagnosed with breast cancer only a month earlier, I wasn’t even sure whether it had totally sunk in, that Fiona said she knew how I felt, her mother had passed away suddenly at about the same time I was getting my diagnosis. She was a young 69, and not just a mum but Fiona’s friend too.

Of course, I wasn’t to know, how could I? But  it was a poignant reminder that we all have  our own problems to cope with. I don’t know why I was sent to  Fiona at that time or how she coped  with me on top of her loss. But she did talk to me about it and perhaps that was a tiny bit of help to her.

So, now nearly bald, I received a scarf I’d ordered online at Suburban Turban  on Thursday.  Yes, there are businesses that specialise in hats and scarves for chemo patients. The scarf is nothing unusual but it is a pretty colour and the right length and material to make into an attractive turban that covers the whole head and, stays in place. Even more importantly for me, it comes with full,  really easy to follow instructions on how to tie the turban!

Old friend and makeup artist, Lesley Chilkes, who grew up next door and whose mum still lives next door to my parents, came round yesterday. We had not seen each other for 8 years, and sadly, that was at her father’s funeral. Before that it was probably 20 years since we’d met.  But there’s nothing like people you’ve known as a child, and after a solid four hours of chatting yesterday, I said it was a shame we’d found so little to  say!!

The chat was interspersed with Lesley giving me some gentle but very useful tips on combining scarves and hats and on making up my eyes. She also very sweetly bought me an eyebrow pencil for when mine fall out, which they haven’t yet done, and showed me how to use the pencil to create soft definition rather than a scary old-lady frown!

We then went out to lunch and tested out the new scarf, topped by a faux fur snood I’d bought recently. Very glam. Interestingly, we didn’t tie the scarf in the full turban style, thinking that a simple  knot would do as an alternative, especially for wearing with a hat. But I realised why ST have gone to all the trouble with the turban instructions, and that’s because their design covers the head better and, more importantly, doesn’t slip.

So I tried the full Monty for the evening. We popped out to the local, The Grapes, to meet friends Sue and Tommy and John and Ross.

I have to admit that despite being someone whose never worn so much as a a scrunchie in her hair other than when doing sport, and who has never really done hats or scarves, I felt glamorous rather than self-conscious. The girls behind the bar didn’t say anything for a while, and I thought perhaps they were feeling sorry for me. Then suddenly they came over and started gushing about how lovely the scarf looked and could I tell the how to tie one like it?

I know that for many women, losing their hair is the hardest bit of the whole traumatic process. But for me, if this as hard as it gets, I’ll be very lucky. Have just ordered two more scarves in different colours. Gloria Swanson eat your heart out!!

Hair loss today, here tomorrow

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My sister was rather pleased with herself for coining the above phrase in response to my mother getting upset when I told her I thought my hair was starting to come out. The hair loss, from the chemo, was a necessary side effect of what will hopefully be a cure, she explained.

I”ve read a few things on the Internet recently where female cancer sufferers, and even specifically breast cancer sufferers, said the hair loss was the hardest of all to come to terms with. At the time I have to say I thought that was a little strange, particularly from someone who was also going to lose their breasts. Surely hair was only cosmetic? And it does grow back.

I’ve been pragmatic about it until now. Not being at all good at wearing hats or tying scarves, I’ve booked an appointment with the lovely style consultant, Morag, who did my colours and style last year. Not only is she thus qualified to advise me on head gear during my months of baldness, but her own sister, a twin if I remember rightly, had cancer and lost her hair.

So I thought I was well prepared. But I’ve had a couple of incidents of alopecia in my life, where I ended up with a couple of bald patches, so I know the difference between the normal amount of hair that comes out when I wash or comb my hair, and an abnormal handful. The latter amount is what has started appearing in my hand, encouraging me to virtually stop combing my hair and bringing the reality home.

A suggestion from the stylist at the clinic was to get my hair cut short first to help with getting used to a new look. I have to be the worst candidate for this hair loss thing in one respect, because I haven’t changed my hairstyle since I was 18, literally! Prior to 18, I had at least experimented with short hair. It was also fashionable to have straight hair, often in a ‘bob’ cut. So I used to blow dry my curls to try to get them as straight as possible.

But at 18, after my treatment for Hodgkins was all over, I went to work in a ski resort in France, where I shared a chalet with 7 French girls who worked with me at the resort complex. One of these had very long, straight blond hair. She would wash it, then bend over with her hair falling down toward the floor and run the hair dryer over it. In less than 5 minutes she was done, while I spent nearly an hour trying to straighten my curls.

So one day, I copied her. And, Lo and behold, I had the sort of curly look that had just become fashionable and that women were paying a fortune in perms to try to achieve. The ease and simplicity — less than 5 mins a day — meant that even when the look went right out of fashion, I stuck with my natural curls.

Now, for the first time in 34 years, my whole look, one that is so recognisable to others, is about to change. I know it’s not all bad. There have been many times along the way when I’ve longed to have a new look, when I’ve envied women who changed their hairstyle every 5 minutes. I never tried because firstly, it’s difficult to maintain a non curly hairstyle when your hair kinks with the slightest bit of moisture in the air and secondly, my husband ‘hates’ it when I do, just for a change, have my hair straightened!

Last night though, that same husband, realising that my hair really was about to start falling out, actually suggested that maybe I should go to a hairdresser and get it cut now. And that’s when the tears fell. It’s never the big things that make you cry. Always the little details.

“It won’t make any difference to me,” Martin said, and of course I know he means it. He’s the best possible person to handle cosmetic changes. He genuinely thinks looks are only skin deep and that it’s what’s underneath that counts.

I guess I should talk to a hairdresser. Trouble is, I don’t have my lifelong hairdresser like some women do. The person who knows me and my hair best these days is my sister-in-law, but not only is she down in Poole, I think she might be too emotionally involved. It would upset her to cut off my locks. Here, I’ve been going to a Russian woman across the road in what is more a barber’s than a unisex hairdresser. She’s fine but her english isn’t brilliant and my Russian really isn’t up to it.

So I’m not sure what I’ll do. But even if I do nothing, I have a feeling it won’t be long before the long-hidden new-look me begins to emerge!!

Sleepless on steroids!

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Have just spent two sleepless nights on speed. Not having ever been into recreational drugs, alcohol excepted, I’ve never experienced such a weird, wide-awake feeling all night. Apparently it’s all down to the steroids I’m on as part of the anti-sickness regime.

Physically I was comfortable and even rested, but my mind was shooting off all over the place. Luckily, no negative thoughts, just lots of thoughts. At midnight I found myself composing a poem in my mind. It was a theme I’d intended to write on, but having composed the whole thing in my head I felt compelled to get up and type it up while I still remembered it.

Needless to say, Martin got a bit concerned by my absence from the bed and seemed even more concerned when I explained what I’d been doing.

The only upshot of the lack of sleep was feeling a little tired today. But nothing drastic. Phoned my wonderful clinic today and a nurse recommended Nytol, hot milk and a boring book! Sounds good to me. Other than that, I’m doing really well. Popped out for lunch with my very dear friend Dena today. She just happened to have two meetings in the area. How lucky was that? And then blogmeister Mason came over to help me configure my new iphone. I have such a fantastic team of people supporting me!!

Taking this all a day at a time, but so far, another successful day. And hopefully, with a little help from yet more chemicals and some hot milk, I’ll get a bit of sleep tonight and be raring to go tomorrow.

So far, so good!

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Well, the first chemo session is over and, more importantly, the day after had gone well. Mum and Lou were with me yesterday afternoon for the first session and apart from the fear of the unknown, I have to say it really wasn’t too awful. Well if it was, I wasn’t given the time to think about it. Anyone who knows Lou knows that she can speak/laugh/joke without drawing breath for as many hours as necessary and even the nurse did more laughing than nursing.

That aside, all went very smoothly and Martin picked us all up at 5pm. Didn’t feel bad when I got home and went to bed around 10.30.

The night was a little challenging, but I’m pretty sure that was as much fear of the unknown than anything else. I awoke at just after 1am to a feeling of total panic. Felt like something was coursing around in my veins and suddenly understood the phrase “waves of nausea”. An odd feeling of sickness/faintness came over me in a wave and then departed. This went on only for 10 minutes. I realised I might be simply panicking, so took a few deep yoga breaths and it was over for good. I didn’t sleep well after that with my brain going ten to the dozen, so woke up feeling rather jaded.

Martin offered to stay at home with me and I took him up on his offer. After a nice lie in, tea and toast and a relaxing bath, not to mention the cocktail of anti-sickness drugs I’d been sent home with, we went for a nice walk up to St Katharine’s Dock and back. It was very therapeutic and I felt much better by the time we got back. I even managed to give myself the little bone marrow injection in my stomach – not bad for someone who doesn’t like needles.

Today was also made much more reassuring by the two calls I received from The LOC (Leading Oncology Care) centre where I’m being treated. The first was from one of the breast care nurses and the second from the chemo nurse who treated me yesterday. How was I? Any worries or concerns?

Last night, my feet had been unusually cold when I got in. I thought about it for a while and then decided to phone the out of hours emergency number just to check. I was called back within five minutes by the nurse I’d met on my pre-chemo visit. “Hi Joanne, what can I do for you?”. He said it was natural that I’d experience various changes in my body while I was going through chemo but to check in with them for reassurance if I was worried about anything.

When the breast care nurse phoned this morning she knew that I’d had cold feet last night. Very reassuring!

I had held out on cancelling the not one but two social engagements I’d had booked for today (why do things always come on the same day or not at all?) because I wanted to stay positive about how I would take to the treatment. There was a lunch with my colleagues at work and dinner and theatre with friends. But after last night I realised that I would be pushing it too far to do either of these today.

There’s going to be a fine line between keeping active and carrying on with life and pushing my body too far, and I’ll have to be careful to keep the right side of that line.

But so far so good. My favourite quote of the week came on a lovely card from my very old friends Pedro and Sarah. It said: “You have a bit of a battle ahead but just remember you have a massive army of friends to help you”! That army, which of course includes my wonderful family and husband (General Ross) has certainly galvanised in the past two weeks and between us, the enemy will most definitely be conquered!! My love and thanks to you all!!

Note to self

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It is possible to feel sick without having chemo! Woke up this morning feeling tired and nauseous and haven’t even started chemo yet. First slug this afternoon. Mother and sister on their way now to collect me.

So I must remember not to attribute every odd little sensation to the chemo. We all have good and bad days regardless of whether we’re on cancer treatment. I think keeping as busy as possible will be the answer!!

It’s all about me, but……. part 2

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Any parent will know that your child can’t go through anything good or bad that you don’t feel you’re living with them. I may not have had my own children but I know this to be true both because I know how my mother feels and because I’m privileged to have step children and grandchildren who’ve given me the opportunity to know how that unconditional love feels.

The hardest thing I had to do once I found out that I had breast cancer two weeks ago was to tell my parents. At 78 and 84, they’ve both spent their fair share of time at hospital and doctor’s appointments in the past few years. Last year, dad had an ankle replacement. A few weeks ago, mum fell and broke her foot. So Lou and I had started caring for them, started making plans for what would happen if and when they were unable to take care of themselves. All the usual things that “middle-aged” (I hate that phrase!!!) children need to consider when they’re lucky enough to still have their parents around.

And then suddenly, it was me, not them. And not for the first time either. They’d already been through every parent’s nightmare when I was diagnosed with Hodgkins’ Disease at the tender age of 17. And again when I was 38 — a major operation and 44, two more ops. This time, I was fit, healthy, enjoying life and hoping upon hope that mum and dad would both make it to their 60th wedding anniversary on June 15th 2012. Suddenly, I was having to find a way to break the news to them. Guess, what, me again, I’ve got cancer.

I phoned my sister first. The most neurotic person you’d care to meet when it comes to me. Ever since she, as a 15-year old had to cope with my first illness, she’s tried to wrap me in cotton wool, phoning several times each day and worrying about nothing. But of course, when I phoned to drop the real bomb shell, she was calm and strong, and has been ever since. We agreed that I had to tell mum and dad sooner rather than later. Before I could pluck up the courage to phone them I phoned a couple of friends. I had to practice saying the words on someone who was not so emotionally involved.

And then I told them. I can’t even remember what mum said. I don’t think she broke down there and then. But over the next few days my sister took the brunt of the upset, while they tried to keep it together when talking to me. Nothing I can do can make it any better for them, except come through this and beat it. Which I will do! But it’s easier for me. I’m the one who can do something each day, who can get stuck in and fight the fight. They can only sit and wait, and, I’m sure, pray.

Once again, it’s all about me but it’s equally about my lovely parents too. If there’s a downside to them still being around for me, it’s only that I have to see them suffer this.

It’s all about me, but……….

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The past couple of weeks and the next six months can feel like everything centres around me, me. me. After all, it’s my cancer, me who’s having to go through all the tests and treatment, me who might feel rubbish some days and hopefully high as a kite on others.

But spare a thought for everyone else affected by my illness. Not least, of course, my husband, my elderly parents, my younger sister and her partner and indeed all my relatives and friends.

Let’s start with my husband Martin. We’ve been together for more than 28 years and married for 15 of those. I was 24 when we met and he was 33. Like any couple together for that length of time we’ve had our ups and downs. Something very strong has kept us together through all that but it’s easy to take each other for granted. Until one of you is diagnosed with cancer, that is.

Martin came with me to the first consultation with the breast surgeon but was unable to park his taxi around Harley Street. So he sat outside. The doc was delayed for about 45 minutes and I was in with him for 15 to 20 mins. In that time he left me in little doubt that he thought it was cancer. He was not sitting in his usual consulting rooms so he sent me across the road to see his secretary and get all of the tests lined up for early the following week (it was late Friday afternoon by now). So I had to leave the consultation rooms and stick my head through the taxi window and tell Martin: “It doesn’t look good, he’s seems pretty certain it’s the big C,” and then disappear over the road to sit waiting for the secretary while she dealt with a previous patient and numerous phone calls. I was probably there for at least 40 minutes in total, leaving Martin alone in his cab to take in the devastating news I’d just given him. By the time I joined him again he’d gone into overdrive. Did I still want to go away at the weekend (we’d planned to go down to Ramsgate?, our usual weekend retreat, where we had a party to go to on Saturday evening and the grandchildren and friends to see). “You bet I do,” I said. I couldn’t bear the idea of sitting around moping about my situation. A party would be the very best thing to do. Was I ok to pop into the supermarket on the way home? (Martin does all the cooking and his daily routine is to pop into Waitrose and choose something lovely for dinner. Maybe because I have been through this before to an extent (Hodgkins’ Disease when I was 17), I instinctively knew that the only way to cope with this was to carry on as normally as possible until something actually prevented you from doing that.

So we went to the supermarket. And as luck would have it, there was a pop up frock shop right next door! Ok, when I said carry on as normal I didn’t mean that you can’t milk the situation just a tad!! “I’ll just have a browse in this shop while you go to the supermarket dear,” I said angelically. But he knew. Twenty minutes later, I’m in the fitting room with a fab frock on and I hear the door open. “Is my wife here?” a slightly concerned voice says. “Ah, just in time,” I shout, and emerge in said dress. Well he’s hardly going to refuse me, is he?

Since that day he’s been absolutely wonderful. Loving, caring, strong. He took me away for a lovely weekend to Brighton this weekend before the treatment starts. He’s staying positive with me. But underneath all that is a man who is hurting beyond belief. He knows how tough it’s going to be for us both to accept the changes to my body that will come about after the surgery. Neither of us will entertain the idea that I won’t get through all of this. But that doesn’t mean that at the back of his mind the whole time is the nagging fear that maybe his mate, his friend, his “secretary” (well we’re all good at some things and poor at others), might not always be with him.

Luckily, this is the modern world. No longer is the male partner ignored in all of this. Everyone has asked after Martin too. Our male friends, far from running a mile at the thought of having to talk about this, have all hugged me and been there for Martin. People are at least aware that men have feelings, very strong ones at that. But for all that, much of what is to come is going to be all about ME. And that won’t be easy on those I love.

The Big C!!

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So, here we go. The last two weeks (is that really all it’s been?) have been the proverbial “rollercoaster”. Sounds like a cliche, but it’s the only word that springs to mind to describe what I’ve been through since I sat in front of Mr Robert Carpenter on Friday afternoon, 25th November, and heard him say: “This is worrying”.

In just 15 minutes, he had decided, and therefore left me with little doubt, that the concerns I’d had myself about changes to my left breast, were almost certainly due to breast cancer. I’d booked myself in for a regular mammogram knowing there was something bothering me. I then asked to bring the scan forward and had it done at Bart’s on Wednesday 16th. Just six days later I had a recall letter and my stomach churned. This was no coincidence.

Not content to wait a moment longer than necessary, I called my cousin, a GP and a font of knowledge about the right specialist for the right job, and, thanks to my company’s private healthcare scheme, was off to see Mr Carpenter two days later.

But this all happens to other people. Not to me! You hear about and read about the blow, the shock that comes with a cancer diagnosis, and you just don’t take it in, because that’s for other people. And this despite the fact that I had Hodgkins’ Disease at the age of 17. So you could say I should have been prepared for this. But to tell the truth, I thought I’d had my meeting with cancer and overcome it. And everyone close to me must have thought the same. Because all they have said since I had all the tests in the few days after meeting Mr C and had the dreaded confirmation, was, “why do you have to go through all this again?”

I could ask the same, but that would not help anything. Right now, I have to think only positive thoughts, and “why me?” is not one of those. It’s me again, get over it.

I have been through untold terror in the past two weeks, none more so than when I went for scans of my lungs, liver and bones to see if the cancer had spread. Life has a strange way of shifting your perspective. When I was told the cancer hadn’t spread, I was so unbelievably relieved that I “only” had breast cancer, it was incredible. Eight days earlier I’d have been devastated that it was the big C. Now I was grateful and relieved that it was contained. And so was my husband Martin, my parents Barbara and Monty, my sister Louise and all of my relatives and friends who are now on this journey with me.

People have galvanised themselves into action so quickly. It’s amazing. My friend Gilly came with me to my first three tests on Monday 28th, sister Lou and her partner Bev were there for the bone scan etc and the offers keep flooding in. I’m so lucky to have such a great support team!!

So Martin took me away this weekend to Brighton to spoil me before the treatment starts.

Tomorrow I have to go in for a little procedure to insert a “port” under the skin, through which they’ll be able to do all the blood tests and administer the chemo.

Tuesday morning I’m back up to Harley Street to see my wonderful oncologist, Alison Jones, and then the nurses, plus am having an echo cardiogram. Then on Wednesday afternoon I’m having the first chemo session. If all goes to plan I’ll have one every two weeks for 16 weeks. Then there’s surgery to come (subject for another day) followed by radiotherapy.

Am I scared? You bet. Am I positive? You bet. I intend to get on with my life to the best of my ability and I WILL NOT let the chemo get me down. As to the final outcome – I ain’t going nowhere!! I’ve got loads more to do in this life and I will be around to do it. No question.

So let the battle commence. I don’t know why I’ve been chosen to fight this war, but fight it I will. And on the way I’m sure there will be much that is positive!

I will write this blog as part of my therapy, and to keep my friends and family updated, and if in the process I can help anyone else who’s going through what I am, then that would be great too.

Jo