End of chemo, almost

This is just so hard. The tiredness is relentless. There’s only a couple of weeks to go but there are times when I feel like giving up. But I’m not and I won’t. I know there isn’t really an option so I just have to somehow get through chemo no 77 and 78 and the debilitating side effects.

As I’m constantly shattered my goal most days is just to have a shower. Having a shower AND washing my hair – now that is a big achievement. I was warned about being totally exhausted but I didn’t think it would be this bad. Perhaps I did but I didn’t want to believe it. If I fully appreciated how awful it would be, then I might not be doing this all again.

A while ago I had an enforced week off from chemo and it was brilliant. It really helped my immune system to recover from all the evil chemo cocktails. Mentally it was great to have a break from the seemingly never-ending treatment. It also enabled me to remember what it’s like to feel well and realise that this chemo will come to an end.

Another reason that it can’t be over quick enough is that my hair is starting to fall out. I was told that my hair would thin but I wouldn’t go bald. I suppose thats what’s happening now.

There are noticeably more hairs on my pillow but I’m not too worried. After having my hair fall out three times, I know that what’s going on should not alarm me. It’s not coming out in handfuls. But even so, I don’t like it. I just try to ignore it, safe in the knowledge that I still have lots of hair.



One thing that’s me helped each week has been a random act of kindness. Back in April I wrote about how fizzy sweets really helped. My anti-cancer drugs are very toxic because they are made from heavy metal and this gives you a horrible taste in your mouth.

A couple of days after that blog post, my friend Keith sent me a load of different fizzy sweets in an old fashioned sweet shop jar. I got the surprise parcel one night after a long day on a drip. I’ve been taking a bag of them with me on each trip to hospital. Cola bottles and fizzy fruit balls are the best. They really do the trick. But they are extra special to me as it was such a lovely gesture.

Now the sweets have almost gone and I have just two more chemos to go. The sight of the almost empty jar makes me very happy that the treatment will soon be over.


Chemo mini-break

I’d been seriously thinking about taking a week off as the chemo had got so exhausting but that decision was taken out of my hands. Last week as usual I had blood tests when I arrived at hospital. These are to make sure my body is well enough to cope with the evil cocktail of drugs.

I knew that I’d been feeling awful for several days. It turned out that I really was properly ill. The results showed that basically my immune system was too poorly for chemo. For anyone interested my neutrophils were 1.4. It means that I am have neutropenia and much more susceptible to infections.

At hospital I was told that I should spend my time off resting. After a magnesium drip I was sent home. It felt weird, almost like I was skiving. I hate the chemo but I was mentally ready for it. Instead we got to go home early.

I was warned that having the week off could make me feel much better so I shouldn’t over do it. But there’s been not much chance of that.  For the fist few days I just felt knackered and mostly snoozed on the sofa.

The biggest change is that I’m not attached to a bottle of chemo which needs to be carried everywhere. It means that this has had a week off too.


It’s brilliant not being connected to the bottle 24/7. My port gets a valuable week off too. Thats the thing which is buried in my skin and where the needle goes in and connects a tube to the bottle

I’m so aware of having all this stuff attached to me that it’s strange to not have to worry all the time. Usually I have to make sure I don’t move my right arm too much otherwise the needle could pop out. I have to be careful that the tube doesn’t catch on anything, especially door handles. Every time I stand up I need to remember to have that stupid bag wrapped around me.

After almost a week off I am starting to get a tiny bit better. Getting your brain and body back is an incredible feeling. Suddenly your head clears and you can move around a lot easier. It’s not all good though. When you’re really ugggggh you tend to focus on how horrible you feel. However when you’re not so ill, you become much more aware of normal life and what you’re missing out on. It becomes tantalisingly close but it’s still just out of your grasp. But even so I’d much rather feel like this than really sick.

I know that my chemo mini-break must come to an end soon. Despite how dreadful the drugs make me feel and how inconvenient how the bottle is, I really hope that I’m well enough for the toxic treatment this week. I don’t want anymore time off. Well I do, but i know thats not the best option for me. This stuff is helping to enable me to live longer and however awful it is, I need to finish this course of chemo.

Chemo no 73


Chemo is such a long hard slog. I’m now more than half way in but there are still far too many weeks to go. The drugs are working and my cancer is now stable which is brilliant. It makes the treatment so much easier to deal with.

Apparently I’m coping well. By this point most other women on the same regime take a break. I was determined to push through and get this finished as soon as I can. Although now I’m not so sure.

Part of coping with chemo is accepting this new reality. You can’t live life like you want to. But it’s so boring. You’re too knackered to do much.

One thing I do occasionally is to draw flowers. Like those above. Focusing on the tiny details of the flowers helps me to forget about the bigger picture.


The worst side effect is the tiredness. It’s just horrific and relentless. Most days I’m just wiped out. Often my body is exhausted but my mind isn’t. It’s frustrating. You want to do stuff, your brain tells you can do things just like you used to but physically it’s impossible.

The trouble is that I now have  a dangerously low level of magnesium. My latest blood test result for it had to be double checked as it was unbelievably bad. As my body can’t retain it and the toxic drugs only make this worse theres not much we can do other than regular mega dose drips of magnesium.

The chemo also has an impact on my already rubbish digestive system. I’m on a low fibre diet anyway. I eat hardly any fruit or vegetables. Due to all the treatment I’ve had my body can’t cope with anything which is too hard to digest but now I have to be even more strict. The other week I ate part of a peeled raw tomato. Bad choice. It made me vomit for a couple of days. I know it sounds ridiculous that something so innocent, something healthy can make me so ill.

Generally most people having the treatment are exhausted and this is made worse by the cancer killing drugs. Chemo is often a long, dull day sat in a room full of ill strangers. So it’s understandable that you do what you can to pass the time.

Phones are great for entertainment but recently everyone on my ward had to put up with a visitor playing lots of video clips out loud. At the time all the patients including me were trying to sleep but with each new clip I woke up. I’ve even sat next to someone who talked to a friend for half an hour with their phone on loud speaker. I mean seriously, do you think any of us wanted to listen to both sides of your boring conversation??

Please, please don’t put your phone on loud speaker on a chemo ward, use headphones instead. Otherwise you’re just being selfish.

Okay, rant over. Did I mention that chemo can also make me quite bad tempered!

No 5 on the List for Living

I’ve done two big things since I last updated my blog. I had that dentist appointment, the one I wasn’t sure if I’d make. Not only did I have the check-up but I didn’t need anything doing – yay!

It was a quite unusual feeling to be in a kinda medical setting with the white coats and the white walls and the smell of heavy duty cleaning products…. to be told that there’s nothing wrong.

It was a pain free celebration of still being here six months on. But still it was going to the dentists and it’s never that pleasant.

The other thing was a lot more relaxing…..

5) Recover from chemo on a ridiculously perfect beach

This must be the most chilled out way that I’ve ticked something off my List for Living!

Holidays are not just about going away; they’re also about having something lovely to look forward to. The thought that at some point my treatment would be over and that one day I’d be able to spend time at a brilliant beach and just gaze out to sea, helped to get me through the chemo.

I went to Cornwall with my friend Anna. This is one of my favourite places. The scenery was stunning and the beach wasn’t busy. We did a whole load of nothing. Perfect.

With the other things that I’ve done off my wish list there was a sense of – wow I can’t believe I’ve done that. This, however, was more a case of I needed that. It’s number 5 on my List for Living. That shows how important this was.

It’s now two months after my last evil chemo cocktail and I’m still so chronically tired. I don’t think I realised just what an ordeal I’ve been through. My body is still trying to make me understand. This is the most exhausted I’ve ever been over such a long period.

This break not only enabled me to get a bit better. You could also say it draws a line in the sand. The last horrendous six months are over. The holiday has allowed me to separate that time with now. Hopefully this half of the year will be about having a more normal life and enjoying a lot more views like this.




I quite like Mondays. It’s the start of my super short week. I’m now so incredibly tired that my week only lasts for two days. Basically I feel sort of normal on Mondays and Tuesdays, and then the treatment begins again. Weekly chemo feels relentless. I’m spending most of my time in bed. I just want it to end. Last week it nearly did.

A couple of days before I was due to have chemo#13 I thought something I hadn’t thought before. For a few brief moments I decided that I didn’t want to continue.

I felt so ill and frustrated by the horribleness of it all. It’s not just the toxic drugs that are so awful but all the other stuff too. Last week I spent around 12 hours over three days at hospital with scheduled appointments, procedures and tests.

When I woke up the next day after the wobble, my symptoms seemed to have faded a little. I wasn’t so exhausted and I knew that really didn’t want to end it early. Even so I came up with a list of pros and cons. I realised that there is only one thing that matters, it’s first on the list and outweighs everything else.


*It’s hopefully helping me to live longer

*Chemo makes me feel that I’m doing something to fight the cancer

*Somehow it makes my skin glow. I know this is totally ridiculous but everyone tells me that I look really well when I actually feel so ill…


*Extreme fatigue, most days I’m close to collapsing

*Lots of random pain all over my body, especially in areas that I’ve had surgery

*Fingernails and toe nails hurt and feel like they’re going to fall off

*Fingertips are a bit numb, meaning I’m clumsier than normal

*Painful pins and needles in my feet and hands

*Breathlessness, I can’t really walk and talk

*Painful to walk and I can’t exercise like I used to

*It’s making my hair fall out

*My eyes are watery and sticky as I only have a few eyelashes are left

*Constant bleeding nose

*Comprised immune system and I could end up dangerously ill if I get an infection

*Steroid induced mood swings


*Disgusting taste in my mouth

*Dizzy spells


*Always starving thanks to steroids

*Chemo weight gain

*Mouth ulcers and sensitive teeth

Now that’s some list. The treatment is truly horrific. You need to be totally convinced this is what you want. I am but it doesn’t stop me from sometimes pretending that it’s not happening.

Before chemo#13 started there were lots of things I had to do at hospital. They required me and mum to navigate the confusing corridors which link the mass of buildings together. On our way back to the ward we made a break for freedom!

Instead of following the signs we left the hospital for an outdoor detour. The morning sun warmed my skin and I felt amazing. For a moment I wasn’t a patient. I was someone out for a walk with their mum, trying to convince us both that we weren’t lost.

As we weren’t that lost, it was soon back to reality. It was the first time I’d faced the toxic drugs after questioning whether I wanted to carry on. As I was hooked up to the drip I knew I wanted to continue.

Some people have been in touch with me on the blog to say that their elderly relatives are refusing to have anymore chemo and they don’t know what to do. I can only really talk from my own experience.

For me the most important thing is being able to have a good quality of life. Aside from the cancer, I’m a fit and healthy 41 year old. I feel very resilient. Despite the long list of chemo cons, I’m lucky that my body is capable of withstanding the treatment and I’m coping well. However, I know that I’ll probably need more and more evil chemo cocktails after this course finishes and in the future I may feel differently. There may come a point when I decide that I’ve really had enough.

This is such a personal decision. I’m convinced that I’m doing the right thing. I feel that I have so much to live for. Whatever it takes, I’m going to make it through the remaining five sessions of chemo.

Chemo #1

I walked into the hospital with a sense of dread. This was my third round of chemo. I wasn’t worried but I just didn’t want to be there. I shouldn’t have to do this again.

There was a big queue to get checked-in. People were crowded around the reception. The hospital reeked of cinnamon, for me this is the sickening smell of chemo. I felt like I was going to collapse from the stress of it all. I wanted to shout, I’m going to faint if I have to stand any longer. Don’t you know I have cancer? But then so did everyone else so I kept quiet.

It was just a small wobble and I had my friend Tamsin with me for support. We drank cappuccinos and talked about happy things, anything other than cancer. Tamsin had brought me some lovely presents including a notebook to write my new List for Living.

The staff on the chemo ward were pretty much the same. Last time I was there I had my own hair. Despite wearing my Raquel wig for chemo#1 some of them still recognised me.

“Hey how you doing? You look well,” one of the nurses in a dark blue uniform said to me with a smile. I wanted to reply that I was only visiting, that I’d popped in to say hello.

“I’m back again for more.”

“Oh…..” Her smile disappeared.

Not much had changed at the chemo cocktail bar. The patient patrons were still mostly pensioners but at least there were some new high-tech reclining chairs.

Setting up the medical equipment, my nurse found it hard to get a vein. The chemo is delivered through an IV drip via an orange tube. My veins are rubbish and seem to run away at the sight of a needle. As my arm was gouged by the nurse, I looked away and towards Tamsin. She offered to pinch my other arm to take my mind off it. Now that’s what friends are for!

The chemo is so toxic that a collection of other things are pumped into you first to prepare your body. I was warned that one of them would make me sleepy. It actually made me feel drunk, properly end of the night and need to go home drunk. And I hadn’t even started on the evil chemo cocktail.

I pressed the recline button and settled back into my chair. I couldn’t keep my eyes open any longer.

It was time to visualise James Bond shooting the crap out of my tumour. It seems that I’m not the only one. A woman called Nicky sent me a message to say that when she had chemo she imagined Vera Duckworth from Coronation Street running around her veins killing the cancer with a rolling pin!

I slept almost all the way through the chemo. Now that’s my kind of a cancer kicking work-out.

I was woken by a loud man on the other side of the room who was visiting an older lady. I felt dizzy and disorientated as I came round. I watched the loud man talk to the nurses and other people’s visitors. He alternated between patronising and sleazy. What an idiot. If you’re visiting a cancer ward, then please shhhh, don’t shout. You don’t want to get on the wrong side of someone who’s under the influence.

As soon as the drugs were done, my friend and I made a swift exit.

Like before, I’m recovering at my parents’ house. Last night I slept in my childhood bedroom – the same place that I retreated to after all the previous cancer treatment. It’s very sad to be back in my old bed again because of chemo. But at the same time I have amazing parents who look after me. Not everyone gets that kind of support when they’re ill.

And very importantly I’m lucky to still be alive. I first had the disease when I was in my late twenties, since then I’ve been living under a cancery shadow. There are many times when really it should have killed me. Despite doing this all again I feel so very fortunate. I still have options.

Earlier I walked around the frosty garden a few times. When I’m recovering from treatment I always try to do some exercise. Compared to when I first did this after my massive operation last year, I now have masses more energy. I even jogged the final lap. Just because I could.

Most of the day has been far less energetic. It’s passed in a tired and dizzy haze. There’s a certain type of Ukrainian vodka that makes me feel like this and so I’m pretending to myself that this is just a hangover.

However this is a happy hangover. Getting a third cancer diagnosis was a huge shock but now I feel empowered. I’m back on the chemo cocktails and blasting that tiny tumour.

Hello chemo, again

Oh chemo, how I haven’t missed you. It’s only been 21 weeks since we were last hooked up. I didn’t think you’d have me back so soon.

It’s been a strange few days as I’ve been preparing to start this toxic treatment again. You may have read about this blog in some of the newspapers following my post on Friday. Wow, what a response. It’s been incredible. Thanks for all the messages. Sorry that I can’t reply to each and every one, it’s just been overwhelming. But they really do help to lift my spirits.

Seeing the facts in black and white somehow made them seem even more shocking. It was as if they were talking about someone else. How can something so terrible be happening to me when I feel so full of life? The headlines were about my ‘months to live’. Yes, that’s a possibility but my focus is firmly on the ‘years to live’.

I’m sure it was difficult too for those close to me. Although some of my friends found it amusing that the papers had used an unflattering photo of me. They knew I wouldn’t like it and they were right. I think it’s great that my friends can still make fun of me. This is lovely, if slightly embarrasing, normality.

Anyway, just to redress the balance, here’s one of my favourite pictures of me. Here I’m reporting for BBC Breakfast. If there are any more stories about me then I hope they use something like this rather than a screen grab from the TV!

Many people have offered to help me with my List for Living. This is fantastic. I’m still working on that list; it’s getting longer and longer. Plenty of people have selflessly offered to help me find unsuitable men. Thanks also to all the unsuitable men who have put themselves forward!

So, it’s chemo #1. As this is the third round of the treatment I’m not especially worried. I’ve had this chemo drug before and I know the drill.

When I was here before I hoped I’d never need any more evil chemo cocktails, now I know this is part of my life forever. The best way to cope with this is not to see it as a big deal. I’m going to think of chemo in the same way as I used to think about the gym. It’s something I have to do every week. I don’t really want to go but I know that once I’m there it won’t be too bad; it’ll help keep me healthy and only take an hour or two. Chemo is my cancer-kicking workout.

Just like before, it will be a chance to catch up with friends. I know I shouldn’t admit this but last time I had so much fun with my friends during our chemo coffee sessions. I actually quite enjoyed being at hospital.

Mind you, there’s going to be one significant change. There will be no cake. Last year I ate lots of it so that cake would be forever associated with chemo and I wouldn’t fancy it anymore. We called it chemo-cake-therapy. Well, it seems to have worked. I just don’t want to eat cake anymore.

As usual I spent the night before chemo thinking about James Bond. Of course this is Daniel Craig as 007. I visualise him killing the cancer. This time it’s a whole lot more violent. James Bond has the biggest baddest machine gun. I picture him pumping the tiny tumour full of bullets. Obliterating it.

As regular readers of my blog will know I have a thing for Bond. I even managed to go to the premiere of Skyfall last year.

It was in October, slap bang in the middle of a glorious few months when I was recovering from treatment and cancer free. I’d give anything to be able to go back to that time.

But I have to think about the future.

I’ve been really inspired by the messages that I’ve had from fellow cancer fighters. The people who’re still alive and defying the odds. One lady in her sixties told me how she’s been beating ovarian cancer for almost fifty years. Others have described how they’re living well despite having a looming best before date.

These are people who’re not just surviving but thriving. I’m having this chemo so I can become one of them.

Back for good

These are the words I never ever wanted to write again. I have cancer AGAIN.

When I first started this blog last March I wrote something very similar. Back then there was hope. I went on to have so much horrendous treatment. I really thought that I’d killed the cancer. Now it turns out that the cancer will kill me.

This is the third time I’ve been diagnosed with the disease. I have advanced cancer, the kind you can never get rid of. All I can now is try to destroy each tumour every time I get one. I’m not terminally ill but I will die a lot sooner than I ever imagined.

The crazy thing is that I feel so well and yet I might be dead by the summer.

The worst case scenario is that I have six months to live. So little time. I’ve been told that it’s a good idea to ‘get my affairs in order’. That’s such a hateful phrase. I’ve started to write my will and think about my funeral. You may be finding this hard to read, I’m finding it almost impossible to comprehend that this is actually happening. It’s unbelievable. This is the most difficult thing I’ve ever had to deal with.

Can it really be months?? I’m an optimistic person and I just don’t think so. I reckon it’s better to believe that I have ages left to live and be proved wrong, than think I don’t have long and be proved right.

Even so, I have to be realistic. I probably only have a few years left to live. Most likely I can expect five years. Maybe ten or more if I’m very lucky.

As you can imagine I’m utterly devastated. I feel upset, angry, emotional, sad…..it’s just so unfair. I cry so often especially when I break the news to someone. It’s all so traumatic. At times it seems like my head is going to explode as I have so many thoughts swirling around. Right now, the world seems pretty meaningless and irrelevant. Nothing really matters.

It was all so different a few weeks ago. I celebrated my D Day. It was 11 years since the first time I was diagnosed. A big happy cancer-versary to me. To be honest, I didn’t really celebrate too much as the next day I had a check-up with my consultant, The Professor. It was a scheduled appointment, three months after my last one.

“Any symptoms, any pain?” The Professor asked as I sat down in the bare white room.

“Well, some. A little pain near my scars from the operations,” I casually replied not sure whether it was serious enough to mention it.

“Right, you need a scan straight away.” He didn’t need to tell me anything else. The way he looked at me said it all.

And that was it. The moment my life changed forever.

It was at that very second I realised the stupid cancer had returned. I desperately wanted to take my words back. I tried to persuade The Professor that the pain wasn’t really that bad. I’d only had it occasionally at night for a couple of weeks.

“No matter what you say, you need a scan, you won’t convince me otherwise,” the consultant told me firmly.

Of course I had that scan. As I waited for the results, I was overwhelmed by worry. I’ve never been more frightened.

A few days later it was Christmas Eve and I was back at the hospital for the results. The nursing sister brought round a plate of homemade mince pies but it just made the grim atmosphere seem even worse. Only the urgent cases were being seen. Why else have an appointment on this day of the year?

Just as I feared the cancer had come back. Or maybe it never really went away. The tumour is tiny. Just 9mm. It’s so small, I could barely see it when I was shown the scan. Precisely 11 years and 1 day after being told I first had cancer, I have it again in exactly the same spot.

What I felt was likely to have been the tumour growing inside me. With ovarian cancer you normally don’t get any obvious symptoms. That’s why most women die from the disease. It’s incredible that for the third time in a row, my body had told me about a tumour.

This shocking news is still just sinking in. I’ve had a few weeks to start to come to terms with it but it doesn’t seem real. Next Tuesday though the reality will hit me. I start another round of chemotherapy.

My hair will fall out; I’ll get sick and be so incredibly tired. But my time is limited. I can’t afford to put on my life on hold any longer. I want to carry on as normal as much as I can. I’m still going to work, and plan to drink the odd cheeky vodka and flirt with unsuitable men. Maybe not all at the same time!

When I had cancer the first time I came up with my List for Living. It was a five year plan of things I always wanted to do. Thanks to the list I became a BBC foreign correspondent and had the most amazing adventure abroad. Now that the cancer is back for good I’m so glad that I followed my dreams.

I’ve been writing a book about my List for Living. I want to get the book published so doing that will be going on my new list. Every day I have more Ideas about what else I want to do before I die. Some people have asked me if there is anything they can do. Once I’ve come up with my new list, you could always help me with something on that.

I want to have fun and enjoy my last few months/years. Especially as chemo will now be a part of my life forever. It will keep me alive. The aim is to shrink the tumour and all its friends that follow. I will have an evil chemo cocktail every week for 18 weeks in the very same hospital as before.

It’s a case of here we go again. It’s so frustrating after all I’ve been through. With this stage of cancer my treatment options are limited. There are only a few types of drugs that can help me. This is terrible, terrible news but it could be worse. I could be terminally ill.

I know how I’m probably going to die and roughly when it’ll happen. It’s weird having a likely expiration date. I really hope my Best Before is at least 2023. But you know it’s not the years in your life that matter; it’s the life in your years.

Once I have my affairs in order I’m not going to dwell on the dying, I will soon have a new list and a whole lot more living to do.

A perfect ten

Dolphins. How I dread those hospital dolphins.

They swim along the corridor on the way to the chemotherapy unit. Even the ceiling has been painted to make it seem as if you’re under the sea. It may look tranquil but just seeing the dolphins made me feel completely drained.

There might as well be a neon sign that says CANCER? COME THIS WAY….

As if that wasn’t bad enough, towards the end of the corridor it starts to slope upwards. It takes every last bit of your energy to walk the last part of it. Mum had come with me. My arm was through hers as we slowly made our way up the corridor.

It’s been a month since my chemo ended. I was there for a final check-up to find out for sure that the toxic treatment had been successful.

This is where I was told I had cancer. More than six months later I was back in the same room and in the same chair. Mum was next to me, also in the same seat as before. I felt so sick that I thought I might have to run out of the room.

However I was so focused on what we were about to be told that I felt compelled to stay. As far as big moments go, this was pretty massive.

If I got the all clear, then I’d be done with the disease, the doctors and the dolphins.

But if I didn’t, then it would mean that those evil chemo cocktails hadn’t worked. We’d have to try again. Jump through more hoops. Worse still, it could suggest that the cancer was terminal and that putting any amount of poison into my veins wouldn’t kill it.

At the hospital there’s a team of people involved in my care. For this appointment I was seeing a consultant who I’ve known for years, ever since the first cancer. She’s never had to break any bad news to me. She is the Good Doctor. Surely this must be a positive sign?

I know that the treatment has already gone really well. All the tumours have been removed and my blood test results are back to normal. But you don’t know what could happen next.

The blood test is known as a CA 125. Basically I needed to get a low number. Anything higher than thirty could mean the cancer had come back.

After chatting for a few minutes it was down to business. My consultant looked at my notes, at my records on the computer screen and then back at me as she said the magic number.

I’d scored a ten. A perfect ten.

The Good Doctor quickly revealed that there was also nothing nasty on my scan. It was a stunning set of results. She brought up a different screen on the computer.

“See, your organs look lovely, don’t they?” I had to take her word for it. All I could make out was a moving black and white image of my insides.

She pointed out various bits and pieces. It was a cross section of a healthy body. My healthy body.

“Hooray! It’s all gone!” The Good Doctor threw her arms in the air. We all grinned and punched the air. My sickness went; it was replaced with pure relief.

That’s it. Finally it’s all over.

The treatment has officially been successful. I won’t have another check-up for months.

After lunch in the hospital canteen, oh yes my celebrations are not always Kylie and cocktails, we got a lift home from the flower girl.

It ended where it all began, outside my house with my friend, Chantal in her big flower van. This is how I started out on my cancer journey when she took me to hospital for what turned out to be a life saving operation.

Back then I had no idea just how hard it would all be or whether I’d even be able to defeat the disease. That’s why I originally called this blog – beating cancer, again, hopefully.

I never realised quite how important the blog would become to me. I’ve been blown away by the love and support that I’ve received. I’ve appreciated every comment even though I may not have been able to reply to all of them.

So, thank you.

I’m now cancer free and there will be no more horrendous treatment but I’m still going to continue with this blog.

I’ve been given another second chance at life. Or maybe that makes it a third chance? Whatever it is, I hope that you’ll be joining me as I blog about life after cancer.

From chemo cocktails to cosmopolitans

Could there be a more perfect way to celebrate?

After so many evil chemo cocktails in hospital, it seemed only right to mark the end of my cancer ordeal with some real drinks in an actual bar.

I know I’ve had a few celebrations already but quite frankly I’m going to be very greedy and I’ll be having a whole load more. Don’t worry though I won’t be writing about every single one!

It’s been a few weeks since my last ever chemotherapy and I finally felt well enough to go out with friends. We arranged to meet at a bar in Chelsea. My long blond WAG wig that I like to call Candice was all ready for an occasion just like this.

This was the first time that I’d worn Candice for a night out.

And what a difference it made. Suddenly I’d gone from almost bald to really blond. Putting on the wig not only transformed the way I looked but somehow made me feel better too, almost like a different person.

Lately I’ve been living in headscarves. I find them easier to wear than wigs although they have a certain cancer chic about them. I think I look more like someone who is sick when I have a headscarf on.  

As me and Candice rocked up at the bar I nervously checked out my reflection in the window next to the entrance. Surprised at what I saw, I smiled back. Something special had happened, I realised that I looked totally normal and I haven’t felt like that for ages.

I knew that both my friends, Kath and Anna were going to be late so I ordered myself something. Seconds later, a man at the bar started to chat me up. Really it was just seconds, my drink hadn’t even been poured!

Wow was that down to me or Candice?! Whatever the reason it was my welcome back to single life in London.

I didn’t have to wait too long for my friends, just enough time for the French banker to give me his number. Normally I would have been happy to stand at the bar but there was no way that I could manage that right now so we found a table.

Drinking Cosmopolitans, Bellini’s and the odd Strawberry Mule, it could have almost been a scene from Sex and the City where the girls meet for drinks and gossip in a glamorous bar.

Only, there were three of us. We were English and this wasn’t New York. Although Kath and I have eaten cupcakes from the Magnolia bakery made famous by the TV series. If that counts…no, thought not.

Anyway that was ten years ago. We were in New York to celebrate me beating cancer the first time round. While we were there we came up with a plan about how I could do some some of the things on my list for living. During chemo I’d come up with this crazy list of things I wanted to do when I was well. Within weeks of that holiday I’d moved to Moscow.

Now here we were celebrating again.

Just like back then we talked about the future and it felt good that I can now get on with living.

Before, the most exciting thing I’ve had to look forward to was my next trip to hospital. The chemo has taken place every three weeks. If that had continued then I should have had another session a few days ago.

Knowing that around this time I’d normally be feeling incredibly ill thanks to the evil chemo cocktail, made the drinks taste even better. Compared to the toxic treatment, the side effects were far more pleasant too.