Tuesday 31 March 2015

DING DING ROUND II

Wednesday 25th March: So here we are, ready for round 2 of chemo. I have to be honest, I did not wake up today full of the enthusiasm (if that is the correct word) like I did for the first one. I am not anxious and although I feel ready to go again, this time I have more information and knew what it would be like and to be honest, I really just don't want to go. As I leave at lunchtime, Roxy struggles a little, she wouldn't let go of my hand as I say goodbye. She told me she didn't want me to go to the hospital again...she looks at me with those BIG BROWN EYES of hers. She is 7, she does not fully comprehend everything that is going on, but she feels it. She is sensitive to me. Bloody cancer!  This round my best friend here, Luisa, asks to take me. Now her and I laugh a lot, we laugh too much, we laugh like teenagers at the most inappropriate things and have often gotten into a little bit of a pickle over the years...normally involving too much wine and too much laughing !!!!  We are both mothers, we both have two little girls each and she is about to become a Mum for the third time in August and I love this woman to the moon and back. I am also very blessed to be godmother to her second daughter. We decide to meet up a little earlier, have some lunch together and head to oncology.  We joke that it is our big day out. I get hooked up and we laugh and talk a lot. I worry about her sitting on a chair for two hours being 20 weeks pregnant and she worries about me using a hospital blanket without a sheet underneath (in case it is not clean)!  I will be honest, I feel it this time, almost straight away, I feel the 'plug' going in and I can feel the chemo, I can taste it again and it makes me instantly sad. Luisa tells me I am brave...I do not feel brave, I just have this overwhelming feeling of sadness. I manage to hold back the tears whilst she is with me but when she goes to collect her daughter from school, I have a few quick tears. Chris arrives, both chemo bags & anti sickness meds finished and I get hooked up to Charley chemo pack again for our 2 day affair at home.

...second round in and already I can not bare to hear that camera lens shutting noise he makes...

So Thursday and Friday are pretty much the same as the first infusion. I feel ok ish. I have nausea again and feel tired. I stay at home. I meditate and this helps with the nausea. I try and rest but do help around the house with cooking and household chores, I need my girls to see me functioning. I get unhooked again on the Friday afternoon and the side effects arrive for the weekend...

...as does Roxanne's stomach bug!!! So here we are at 0330 on Saturday morning and the poor girl is throwing up. She is such an incredible child. She is sick on her own and then comes to tell us!! Chris the superhero, gets up and deals with it and looks after her so that I can sleep. I am unable to go back to sleep and stay awake feeling sick until around 0630 and then he goes to work at 8am. Saturday is a TOUGH day. Emotionally I am a wreck this time, I have no idea why it is hitting me so hard but I am very aware that both of my girls need to see a happy Mummy and I do hold it together. Between Madi and I, we do laundry, hang up washing, sort the animals out, tidy up and look after a vomiting Roxanne. Thankfully I am surrounded by wonderful friends that have said they will take the girls off for me on my treatment weekends, so Madi heads off for a fun afternoon/evening with her friend and Roxy stays with us. For me it is so important that both girls are not dragged down by this. Of course I can not shield them from the fact that their mother is going through this treatment, and they do see me when I return from treatment and they know I am different for a few days, so if they can escape for 24 hours over these weekends then I am very very thankful for that and eternally grateful to my wonderful friends that make this happen for them/us.  The remainder of the weekend is a roller coaster of tears, a little anger, a little fear (a new emotion for me on this journey) and a lot of frustration. I said to Chris that I can not understand how I got colon cancer (as if we ever really understand why we get cancer or any illness). I mean, I eat healthy, I worked out. Of all the cancers out there...colon cancer really would not have entered my mind to worry about!  I actually annoy myself this weekend as I had been so in control of my emotions, I was not worried about the future and almost felt as though I did not really have cancer and more that I was just going through this motion, but this weekend I feel different. I feel shit. My body aches. My head aches. I feel sick. Food does not interest me. I am bored with drinking warm liquids as the neuropathy sets my mouth, teeth & throat into spasms if I have anything other than room temperature or above. The neuropathy is actually going through the roof this time and my hands are so sensitive to anything cold. I can't hold anything and my hands start to seize up. I actually drop a knife, blade down onto ASBO's head on the Sunday (trying to cut fruit), both he and Roxy just look at me...ooops. Thankfully he lives and there is no visible sign of a wound!!

Sunday is just sleeping. Sleeping is good, there is no nausea whilst you sleep. More tears...get a grip Amanda this is not your life, this is just a hiccup you need to deal with, but I can't stop them. Chris and I sit and talk a little on Sunday evening. I get a glimpse of his fears. You see because I know that I am not going to die (well we all die, but immediately I mean), I had not once thought about his fear of me dying. It's a real fear. I am his wife and mother of his children, of course over the past few weeks this thought has entered his mind. We do not really talk about it in depth, its more of a passing comment but it has registered with me.

Monday 30th March starts promising... then just goes downhill. I manage to make lunch for 6 of us, a friend and her little girl come over and I actually manage to get out for the first time since last Wednesday, ok it was only to Mercadona food shopping, but I made it.  Totally wipes me out and I get annoyed at my lost energetic self.

Tuesday 31st March. OH HELLO !!! Yep feeling better, not 100% but better. Managed to have two breakfasts this morning and am determined to get my dolly on and get out in the sunshine for a walk. Easter present shopping for my little girls later this afternoon with the hubby, might even treat myself to a cold drink as the neuropathy seems to be passing, although still present in my hands. The sun is shinning, summer is coming, I have completed round II of chemo, I am feeling so positive today again.  I feel today should be about BIG hair (yes yes it is still intact) and LOTS of lip gloss to celebrate that there are only 10 treatments to go ...



No matter how you feel, get up, dress up, show up 
and NEVER give up.








Wednesday 25 March 2015

THE DAYS FOLLOWING CHEMO....

As I said previously, I started feeling more 'me' on Tuesday 17th but had to deal (obviously with lots of help at home) with the littles having flu. So Thursday to Sunday is filled with just looking after them, being with them, making them food, watering them, making them sleep. Madison does however, make a remarkable recovery in time to go to her friend's house for a sleepover on Saturday 21st...promptly climbs into my bed on the Sunday when she returns to sleep it off!!

I am feeling better. I can feel the difference in my body and more importantly in my mind. Not that I didn't have control of my mind (for a change!!), but I do need to tell myself daily that "I've got this and all will be ok". The overwhelming tiredness and nausea that I had the week previously after the first round of chemo has now gone. I am hungry again and have found a love for cooking...anyone that knows me well will laugh at this statement. Cookie (maiden name was Cook and I was lovingly referred to as Cookie by my friends) & cooking have never been a known partnership!!!! I have always been aware of healthy eating but now I am trying to eat super clean and really enjoying making up recipes (and very annoyingly I am posting pictures on Fannybook and Instagram).  I am completely unable and unwilling to follow a recipe, even when making cakes or biscuits previously for my children they laugh at my inability to follow simple instructions...hence the "ooooooh mummy has been cooking again...what is it"? Also, I seem to have complete 'Dora' concentration when it comes to cooking or being in the kitchen. I have destroyed endless pots/pans by putting things on to cook and walking away and starting another task, only remembering once the smoke alarms are going off or I can see/smell smoke coming from the kitchen. Most famous and common are pots of rice & pasta...I mean how can you burn rice!!! Anyway, I am enjoying having the time to explore different ideas, some are appreciated by the children, others are met with a confused look and "nope don't like that'.

I have very dry skin. This I notices straight away after the first round. My hands look like little old ladies hands already and no amount of almond oil, coconut oil or Body Shop Shea Butter is helping, plus the coldness in my fingers and toes seem to be here to stay. Having said that, I am able to eat & drink cold things, well cooler than room temperature, after about 5 days. I was amazed at how quickly the side effects kicked in and they say with this particular chemotherapy, it builds each treatment but I am determined to beat the side effects by clean eating and boosting my system where I can. I guess only time will tell how each treatment affects me personally as it is different for everyone.

One side effect is particularly disturbing for me and this paragraph comes with a TOO MUCH INFORMATION WARNING!!!


Gas leaves the body when people burp through the mouth or pass gas through the anus. Gas is primarily composed of carbon dioxideoxygennitrogen,hydrogen, and sometimes methane. Flatus, gas passed through the anus, may also contain small amounts of gasses that contain sulfur.


You see, I had 48cm (double checked my notes this week) of my colon removed on the left hand side. Things are different now in the bum plumbing area and apparently it is completely normal and usual to now have an unbelievable amount of gas that needs to escape your body. Also chemotherapy plays havoc with your bowels too. It was kinda funny the first few times but it is unbearable now. I am constantly apologising at home much to the amusement of my husband (why do boys find farting so amusing?) and there is always the 'uncertainty' of that unexpected 'gas' as to what is actually happening down there...never assume it is only gas!!!! I feel like Johnny Fartpants from Viz.




I decided that this was the week that I would finally google my results, watch videos of my procedures (colon removal and resection and the port a cath implant) and just generally scare the shit out of myself. I guess I needed to do it. Of course, I completely freaked myself out with the survival stats:

Stage I cancers have a survival rate of 80-95 percent. Stage II tumors have survival rates ranging from 55 to 80 percent. A stage III colon cancer has about a 40 percent chance of cure and a patient with a stage IV tumor has only a 10 percent chance of a cure.



    5-year Relative
    Survival Rate
    I
    92%
    IIA
    87%
    IIB
    63%*
    IIIA
    89%*
    IIIB
    69%
    IIIC
    53%
    IV
    11%



I am IIIb. Chris did remind me that these figures do not take into account age and health. A lot of colon cancer patients are older than 50 and possibly not in as good health as I was to start with. Anyway, these stats are now erased from my mind, I am not a statistic! I make my own rules.




My second round of chemo is today, Wednesday 25th March at 1500. I am going for lunch with one of my best friends and then she will come to the clinic with me. I am feeling completely relaxed about today as I now know what to expect. I am not anxious about the side effects as I know I can handle them. The only aspect which is on my mind is Charley chemo box, not that he bothers me really, it is just an inconvenience to have him attached to me for two days, a little bleeping reminder that you are being pumped full of poison. 


My gorgeous friend Lisa sent me this (she whatsapps me post cards as she is in Hong Kong) and I feel that this is very apt for me at the moment:







Thursday 19 March 2015

IT'S IN MY VEINS

Friday 13th March: I have never been superstitious of this date and I did smile to myself that today would be the first time I am disconnected from my Charley Chemo pack. End of my first chemo session. Friday 13th will always stick in my mind now.

I wake at 0600 with an incredible urge to throw up. Boy I have not felt this nauseous since I was pregnant with Madison. I did joke with Chris that if I could have suffered 9 months of morning sickness everyday, then I could suffer 6 months of this!! The feeling of nausea makes me cry as it is so intense and so violent. I tell myself out loud (seems to be my mantra at the moment) "I can do this, Amanda you can do this". I tell myself this in-between big deep breathes. Chris gives me a reassuring squeeze and then makes me a big mug of hot water with lemon & ginger slices.

I manage to get myself up to send some time with the littles at the breakfast table. I can't eat this morning, I have a very strange metalic taste and sensation in my mouth. The littles go to school and I go back to bed...BEEEEEEP BEEEEEP ahhhh the chemo pack has finished, time to go to the clinic to be "unhooked". Again anxious at this first time experience but as before, gorgeous staff at the clinic and it is done within 15 minutes without any discomfort.

Friday evening is spent with some of my girlfriends.  We are having a little tea party for Sarah's birthday. It's great to see them, we have sushi and cake. I have bought the girls some cava and white wine, I drink pots of green tea. Never thought I would see this day... me drinking green tea on a Friday night with my girlfriends and not pregnant!!! We  laugh so much that it makes my new tummy scars ache and I love it.  By 10pm I'm done, seriously exhausted and I have to ask my slightly merry friends to leave. Madi is out for the night (well for the weekend as she seems to be a lot now), our au pair is away for the weekend, Chris & Roxy both snoring, so I am the only one awake. I seem to be awake a lot in the evenings on my own...damn sleep pattern since the surgery. The quiet night times are when I think about all of this. I sit and watch Comic Relief for an hour and have a cry, but this time the crying was for the children that I see on the screen, that go to work on dump sites everyday, that have nowhere clean to sleep, who look for food on these dump sites... really I have it bloody easy don't I? At least I have health care and a clean clinic to go to and am able to receive the treatment I need. I suddenly have this overwhelming feeling of guilt ...

Saturday 14th & Sunday 15th March: they do say that the "shit" times come after you are 'unhooked'. Well they were right about that and I am surprised at how quickly these side effects have kicked in after just one session. I have hardly any energy, my mind is there albeit a bit fizzy but my body is struggling. My arms and legs are heavy. I do not like this side effect. I am energy. Anyone that knows me will know I have a lot of energy. Not much I can do about it, but to eat good, rest and just go with it.

There is not much to differentiate between Saturday and Sunday, other than Saturday was dark and rained most of the day and Sunday there were the occasional glimmers of sunshine... mirrors well how I was feeling this weekend. Both days start violently at 0600 with that nausea, with that comes the crying. The crying in the morning is beginning to piss me off and in turn that makes me cry more. I say my usual mantra and then spend both days on the sofa watching movies. My port a cath is really hurting this weekend and that is pissing me off too. Basically the weekend is a good mix of crying, dry retching, feeling pissed off with my port a cath, pissed off with the chemo side effects, with the f*&king inconvenience of all of this ridiculousness and then something I say or do (normally this is something to do with excess air...that will be covered in a seperate chapter!) will make both Chris and I laugh and everything seems ok again. Every now and then I take myself to one side mentally and give myself a good talking to. This is only the first one Amanda, get a grip and find your balls.

Monday 16th March: waaaaaaaaaa arrrrrghhhhhhh morning, there it is, the retching. Really tired today. Nothing much gets done. I manage to shower and get into clean PJs and make lunch for the girls. Madi announces that she has a pain in her chest, I feel she has a chest infection, so her and au pair go off to the clinic on the way back to school in the afternoon. Apparently she was seen by a really vile doctor at Clinica Rotger that told her she was not sick or looked sick and said it was a muscle pain. I naturally assume she must have pulled a muscle at the fair the day before. We just dose her up with pain killers and reassure her she will feel better tomorrow.

OH HELLO TUESDAY 17TH MARCH: I am back in the game !!!!!!! I feel fabulous - ok not absolutely fabulous, but soooooo much better and well enough to wash and dry my hair (it's still on my head, no loss yet) and I put make-up on. There she is.  No nausea this morning and I have a lot more energy. Wow, what a difference it makes to your mental well being too. I feel I could conquer the world this morning. Am greeted with a very poorly looking Madi, home duvet day for her. She sleeps, eats, sleeps. Scruffy is also ill, the back terrace indicates to me that he has a tummy bug. So there I am, in my PJs and flip flops with baby wipes and mop in hand, clearing up his bottom which is now covering a good 20% of the terrace. This is what happens when I get smug and feel better!!! Not much improvement from Madi as the day goes on,  so off to Juaneda she goes with Chris. Text message beeps, ¨she has flu¨. My immediate reaction is OMG poor girl and she has her RADA ballet exam tomorrow, Chris´s first reaction is worry for me. I have just finished my first round of chemo and my white blood cells will be low, I can not get sick or I will not be able to have my next treatment. Seriously, my girls are super healthy and the one time we need them to continue to be super healthy and one of them goes and gets the flu!! How selfish ;-)  Madi announces that she will be attending her ballet exam tomorrow even if she has to just turn up to dance and get a pass. We'll see about that in the morning.

Wednesday 18th March: Oh I am feeling good, Im feeling good....oh Madi you look like shit! Poor kid, she looks horrendous, hot and so full of the flu. She has a few tears (get them out girlfriend, I am all for tears) and she announces that she WILL be doing her ballet exam today. My warrior child. Both of the girls have exams today, so we head off and they get them done. A celebratory bacon sandwich seems to be in order for the littles afterwards...bacon makes everything right - well apart from me at the moment, my most favourite thing in the world tastes awful right now...I'm giving meat a miss until my treatment has finished and trying to eat super clean BUT I MISS BACON, OH HOW I MISS YOU AND YOUR RED KETCHUP COVERING.....!!!!! I am feeling super proud of my littles today, they are, in my humble and biased opinion, just amazing. Madi warrior child just takes herself back to bed. She did what she needed to do, she then refuelled and now she will rest. How can you not be in awe of a child like that!

ALERT: 2nd child down with the flu. I now have 2 children with flu and a dog with diarrhoea. I can only be thankful that this is all happening whilst I am in my 'good' cycle. Ok, so if we can just ensure that any more family illnesses fall on the 5th day after my chemo session please, then all will be ok! I am standing in the kitchen with various kids medicines, hot water bottles, dog looking at me because he wants to eat and I am starving him until his tummy is better, ASBO the maniac monster kitten running wild and attacking anyone and everyone and trying to make a super healthy vitamin packed dinner for us all and I can't help but laugh at this situation. In the madness of the last 5 weeks and yes it is only 5 weeks, I am here having a very real moment with people that need me...my family.

Then they come again, those tears. This time angry tears. The anger is what will get me through this journey...because I am angry now that this has gatecrashed my life's party...



Friday 13 March 2015

CHEMOTHERAPY BEGINS

Wednesday 11th March: It's finally here, the day I start chemo. I wake up in a full positive mood, almost a feeling of euphoria that the day is finally here and I can start treatment to get me on the road to me again. I have breakfast in bed and play lots of load music. I could almost go out now and have a good dance with my friends. I write some blog and do some meditation. I feel relaxed. I am ready for this. 

Appointment is late afternoon. My phone is full of good luck messages. Love my family & friends. I am feeling anxious, it's the unknown isn't it? The oncology department in Juaneda is just wonderful, the staff are so attentive and caring (well guess they should be really, considering the treatment they are administering!). So I arrive, see the doctor and I am shown to box 7. Box 7 is nice. I have a big reclining  chair with lots of blankets and pillows if required, 2 guest chairs, a TV with various channels including BBC 1 & 2, free wifi, on-suite bathroom and refreshments available to me. If it wasn't for the fact that I have cancer, it would be a fairly nice place to go for a couple of hours to get away from the usual hustle & bustle of being a busy working mum...

I was anxious for how they would attach the chemo line to my port a cath. They cleaned the area and I was told to take a deep breathe after the count of three and there, it is done. My nurse Laura, is amazing. We get by in English and Spanish and she explains everything so patiently. She laughs at my dark English sense of humour and I just know that we will get on famously over the next 6 months. So the line is in and I have my anti nausea medication first then followed by two bags of the chemotherapy. I'm left to relax. I feel it going into my body for the first few seconds, strange knowing you have poison pumping so freely into you. I used to suffer terribly from severe panic attacks and had a deep fear of dying, so much so that I needed professional help to overcome this fear. So, even now, anything that feels unnatural in my body can set of a panic attack, but I have learnt to stop them within the first few seconds. Well, as I felt that chemo entering into my body, I could feel myself slightly panicking, I had to tell myself it was all ok and Chris gave my feet a squeeze to tell me it was going to be ok.  We get to 7.30pm and it is all done. I am then introduced to Charley the Chemo pack, it is attached to my port a cath and off we go home. I am to have another 36 hours of chemotherapy at home. Back on the Friday 13th to be disconnect from Charley and then the process starts all over again in 2 weeks time.




What is FOLFOX 


FOLFOX is the name of a combination chemotherapy treatment. It is also known as Oxaliplatin de Gramont or OxMdG, which means Oxaliplatin modified de Gramont. It is made up of the drugs
  • FOL – Folinic acid (also called leucovorin, FA or calcium folinate)
  • F - Fluorouracil (5FU)
  • OX - Oxaliplatin

Common side effects (in case you want to know, because I am asked all the time!!)


More than 10 in every 100 people have one or more of the side effects listed below.

  • An increased risk of getting an infection from a drop in white blood cells – it is harder to fight infections and you can become very ill. You may have headaches, aching muscles, a cough, a sore throat, pain passing urine, or you may feel cold and shivery. If you have a severe infection this can be life threatening.  So basically I need to stay away from any germ ridden people. Please always wear a face mask on our lunch or coffee dates, I would but chances are I might be losing my hair so really do not need to draw any more attention to myself!  Don't be vain, cover up :-)                                                                                                                                                    
  • Tiredness and breathlessness due to a drop in red blood cells (anaemia) – you may need a blood transfusion. How do you define tiredness? I was tired before I got the cancer and before I started the chemo. I am a working mother who likes to burn the candle at both ends. Is this drop dead tiredness or just general I can't really be arsed to get out of bed tiredness. We need a benchmark here!!! 
  • Bruising more easily due to a drop in platelets  – you may have nosebleeds or bleeding gums after brushing your teeth. Or you may have lots of tiny red spots or bruises on your arms or legs.
  •  Oh that will be something to look forward to with the summer upon us and little summer dresses to wear, always looks better with an arm/leg full of bruises or spots.  
  • Tiredness and weakness (fatigue) during and after treatment – most people find their energy levels are back to normal within 6 months to a year. 6 months to a year...you are f*&king kidding me on. I need to try and prove this wrong. Surely diet can assist to the rebuilding of your energy?
  • Numbness or tingling in the fingers and toes happens to nearly everyone having oxaliplatin and is usually worse if you are cold. You may have trouble with fiddly tasks such as doing up buttons. This can start a few days or weeks after treatment and usually goes away within a few months of the treatment finishing. Another interesting side effect is that you will not tolerate eating or drinking anything above room temperature and even entering the fridge is hazardous!  Crazy, I ate a banana this morning and it was cold, set my teeth alive with tingling. The same with a glass of water, felt as though my tongue was swelling up. I now have a pair of wool gloves on top of the freezer!
  • Feeling or being sick happens to about 7 out of every 10 people but is usually well controlled with anti sickness drugs. Loss of appetite comes with the nausea = weight loss. Every cloud and all that!
  • Hair loss or thinning of hair. Now I have thought about this long and hard. I love my hair but have recently had it cut shorter to give it some strength. If I lose my hair then I will be creative and can always have a couple of wigs. Husband has always wanted me red and I thought I might flirt with a big Beyonce style :-) In the scheme of things, when I win this battle if I have no hair, then it will be a big bald trophy to show I bet cancer and survived the chemo.
  • Diarrhoea happens to 6 out of 10 people. All I will say on this matter is that Colon Cancer produces all sorts of unexpected bathroom visits. Chris and I went out for a drink before my treatment started and lets just say, it ended with me in the bathroom, half naked trying to wash my jeans and then realising that there was no hand dryer to dry them!!!!!! 
  • Sensitivity to the sun. This should make for an interesting summer. I live in Mallorca and the long hot Balearic summer is about to begin. Oh but don't worry you can drink lots of cold drinks and sit in a cold pool - oh wait, no you can't as you will be suffering with Neuropathy! Ok, so I'll be the skinny bald bird by the pool in a full sunsuit with thick factor 50 sun cream whilst wearing gloves and socks.
  • A sore mouth happens to 4 out of 10 people. Surprised I have not got that yet, due to all the WTFs that have escaped my mouth during this 2 month journey so far.
  • Loss of fertility - you may not be able to become pregnant. WHO FEELS SEXY DURING CHEMOTHERAPY ???????????????


Thursday 12th March: I slept really well with Charley the chemo box, although he does make this strange camera zoom lens shutting noise every few minutes as it gives me another dose of the poison. I start the day with an incredible urge to throw up. Oh the nausea has set in. Surprised it had so quickly. I take my anti sickness tablet, forgetting about the cold drink thing and instantly my tongue and back of throat tingle, very strange sensation, it's almost as if your throat would close and choke you. I get up and spend some time with the littles and au pair at the breakfast table. They brighten my day, all three of them.

My au pair was supposed to go home to Italy in March but after finding out my diagnosis she decided to stay. I can not express how much this lovely soul makes a difference to our house, to my girls and how much it helps me her being here right now. We love you Alessia.

I had a few tears today. They are overwhelming when they come. It feels like a massive wave of grief, but the grief is not necessarily for me. It's just for the entire shitty situation. I want to be strong and I am strong but I can't help but feel like I have let people down by becoming sick. I am not good at letting people look after me, but I truly appreciate all the love and help that I am receiving right now. I cry in private so that the girls do not see me. Mummies are warriors right?  I cry with Chris because he just holds me and knows that it just needs to come out. Madison asked Chris the other day if I will die. No baby girl I will not die. I will fight through this treatment and I will beat Cancer. I am determined to learn something from this experience and it will not become a family member. 



1 DOWN... 11 TO GO !!!


Thursday 12 March 2015

FROM THE BEGINNING - A QUICK SYNOPSIS

Summer 2014. My bloody lower back is aching again..I am nearly 44. Uff is this old age setting in already I ask myself!


I am a mother of 2 little girls. Madison aged nearly 12 (mentally 20) and Roxanne who is 7. I also have a husband, Chris, he works in the yachting industry.   I work full time in an office and we have a nice little life living in Palma de Mallorca.

I like to go to the gym. I like to be busy. I like/try to have total control of most aspects of my life. I am a born organiser and I am very good at multi tasking. I am a strong minded girl, sometimes I let myself down by over worrying,  but generally I know where I am at. All of these will be tested over the coming months.

So I decided to finally take myself to see the doctor as I had been moaning about pains in my lower back and tummy area. It was like a dull ache, not a specific pain. Previously had problems in the "lady garden area" and just thought it was that again. Doctor confirmed I had ovarian cysts and a growth on  my right ovary and she put me on a new medication to shrink them. This was in June, by September I was feeling sick and had headaches, took myself off the medication and she booked an op for December to remove them. November I received a phone call to say that my operation had been cancelled due to my doctor being off sick but they did not rearrange it. To cut a very long story short, I contacted my insurance company, went to see another specialist who informed me after more scans that my ovaries were completely clear and I had probably been ovulating before and surgery was not required!!!!!! This specialist was convinced it was a bone issue. WTF, so would I have gone to hospital in December and had an operation that I did not need...would they have just told me they had removed the problem? 

November was spent feeling very tired, unmotivated and pain was becoming so intense I was struggling at work to sit at my desk. I had stopped my regular gym sessions and sat on the sofa most nights with hot water bottles that my increasingly patient husband prepared for me. Christmas came and went. I felt like shit. Cancelled all social appointments and was generally quite low and feeling unwell.


2015 - Full Steam Ahead!

It was a  Friday in January, can not remember the date, think it was 16th. Feeling particularly shit and in pain at work, my boss insists that I take myself to Urgencias (A & E department). Chris picks me up from the office and off we go to embark on what will become a journey of unexpected conversations and experiences...

Clinical Juaneda xrayed me straight away and confirmed that I had a fractured coccyx, although the doctor did say the pain possibly was not from this as in his opinion, the fracture was very old. To be fair, I have had a few falls over the years... many a good night out ended with the Coleman horizontal, so this did make sense! Booked in to see a trauma specialist the following Monday. Trauma specialist confirms it's an old injury, he believes this is a bowel problem - I was beginning to feel the same way, due to some of the symptoms recently. Bowel specialist is booked for 3 days later and also an MRI scan to check spine etc.

One would expect a bowel specialist to be a middle aged person, not a young sassy chica! That was one internal inspection I found to be particularly uncomfortable... much to the perverted amusement of husband once he saw her! I think she knew on that day what she would find during the colonoscopy that is booked for me the following week. Prescription is written for the medicine to clear out my colon and off I go, none the wiser. 


Now reading up on Colon Cancer, the signs were all there.

OMG. The medication to clear out ones bowels are horrific. All I will say is, the bathroom becomes your new best friend and you wish you had a cooler built into your underwear!!! I was too scared to sleep on the night before my colonoscopy, not because of the procedure but due to the effect of the medication...if you have seen that famous scene from Train Spotting, you will understand...ewwwww!

I am a born organiser ... obviously not Amanda as you turned up 24 hours late to your colonoscopy!!! Not only was I super stressed about having a camera shoved up my bottom, I also had to adopt a duck like walk to ensure I had no embarrassing accidents on the way to the clinic due to said medication, which was still working its magic on me. As we sat in admissions, whilst she looked and shook her head saying "no it was yesterday you were supposed to be here", all I could think of was there is not a chance in hell I am doing another 16 hours attached to a porcelain bowel AND it cost me 40 euros for that bum burning experience. Thankfully for me, sassy bum specialist took pity on me and agreed to still go ahead with the colonoscopy later in the afternoon. All I had to do in the meantime was to try and retain some dignity and stay close to a bathroom.

The best thing about having private medical insurance is that you can ask for drugs (within reason of course) and they will happily oblige. I have a fear of surgery and being put to sleep and although I was not having a full general for the bottom inspection, I still asked for something to relax me. So here I am in the prep room, sporting a very attractive white gown which opens fully at the back (wish I had worn a thong to the beach now last summer as I still have a visible bikini bottom mark). I start to shake uncontrollably. The fear kicks in. I am given my sedative and the floaty clouds and big smile arrive.

"we only managed to go 70cm inside as we found a tumour and yes in our opinion the size and colour would indicate that it is cancer..."

Floaty cloud and smile disappear, we are given an appointment for the following week and Chris and I go home with that sentence ringing in our ears. Surely it can't be cancer, I don't get cancer...do I? I have named my tumour Trevor.

Monday 2nd February: I have a enterography MRI scan (think that is what it was). Have to drink 2 bottles of Pernod tasting liquid which makes me gag then burp uncontrollably. Very ladylike in the waiting area belching and gagging on this vile liquid. Chris laughing like a 5 year old. I also notice that I am, without doubt, the youngest person there! What am I doing here I ask myself. These are all old people waiting for scans, I'm 44. Again nakedness is required, white gown on (at least I have my knickers on this time) and off we go for for my 3rd MRI scan since December. They try to insert an intravenous drip for the medication, however, apparently I have veins the size of a child. Finally find a vein to use after 4 or 5 attempts (breathe in breathe out) and I'm ready to go. OUCH OUCH OUCH my right arm is burning and starting to swell. Hello is this normal I call out... oh no, the intravenous medicine has gone into my muscle and not my vein...I am starting to look like Popeye's sister. They use a blue medical glove, fill it with hot water and strap to my right bicep and insert the drip to the left arm and off we go again. Can't imagine what I look like, laying there with a white gown and a fully inflated blue hand attached to me...where is my mobile, surely this is a selfie worthy picture for Fannybook.

Thursday 5th February: results day. Indeed Trevor the tumour is cancerous but not to worry, it will just be cut out and you will be ok. No chemotherapy or radiation will be required, what a bloody lucky girl I am. Well that's a relief then. Plus, it is done with keyhole surgery, so guessing I will be home the same afternoon. I feel like the luckiest girl in the world and announce this to everyone.

The bliss of ignorance...

Monday 9th February: Appointment with the lovely surgeon who will remove Trevor. Lovely surgeon announces that this is very serious and I will come into hospital today and the operation will be Tuesday evening. Serious? Keyhole they said! Yes Amanda, it is keyhole...easy for me but major  surgery for you. 2/3 hour op and a 6 day hospital stay as we need to remove Trevor (well he said tumour of course) and 30cm of your colon. The first time lovely surgeon receives the "WTF" exclamation from me - it will not be the last time! Well this is a total inconvenience I shout out...lovely surgeon likes this feisty attitude and tells husband I will do well. Anxious lunch with the littles at home (they come home from school for lunch), explain Mummy must have an operation to have a lump removed, but all will be ok and they can come and visit Mummy as soon as the operation is finished. Pack bag, big big tight hugs with the littles and off Chris & I go.

Room is nice. Double room with 2 single beds in case I have a party and someone needs to crash over. I play with the bed controls for a while,  raising head & leg simultaneously...OMG OMG I will go mad here for 6 days,.I am not ill, how can I be here for 6 days. I have children, a family, work, I have a life, I can NOT be in here for 6 days.  I have brought 3 books, mini DVD player and a stack of classic films to fill the 6 boring days ahead of me.  HA HA HA oh yes, that still makes me laugh even now thinking that I would be bored!!!

Second round of colon/bum clearing medicine is administered and then I had to suffer the indignity of having an enema. I already had a smacked arse face due to the drip they had inserted. Surely this is not needed until tomorrow, my operation is not until 5pm tomorrow night I cry out as she puts the intravenous line into my arm and it is put into the inside elbow area (more medically minded friends of mine will know what that area is called), so of course, I can not bend my arm and now I will have the worst nights sleep - well what with that and the toilet dashes!!!  I cry for the fist time, overwhelming sense of why the f*&k am I in here doing this, how can I have a Trevor?  I was on my 238th trip to the bathroom (not easy running fast and clenching butt checks with an intravenous drip & stand attached to your arm!!), when in walked the nurse with a suspicious looking bottle. I knew exactly where that was going! I tried to explain in my poor Spanish that there was not much left inside me, so could she spare me from the enema and she genuinely did look sorry for me and said no, "roll over"...

How long should I hold the liquid in for...as long as you can Amanda...10 seconds after she left the room, I did my intravenous drip sprint to the bathroom... this was going to be a long night again...

Tuesday 10th February: Op Day. Anxious. Relaxed. Anxious. They come for me around 4pm. Familiar faces in pre op room from before, nice to be recognised and lots of hellos and smiley faces. Uff here come the nerves, nice little pre med and I'm back on floaty cloud with stupid grin on face when lovely surgeon man arrives. Gives me a reassuring arm squeeze, mask is put on my face, 2 big deep breathes and I'm under.

Wake up in recovery room, freezing and shaking. Bed is being filled with warm air and people are talking to me. Chris says I came back to the room around 10pm looking rough and talking rubbish. Sounds like how our Sunday mornings post clubbing used to be in London!!

Wednesday pain. Oh the pain. Give me the drugs. I know I had visitors, 2 being my children, the gorgeous Melanie (Roxy's first amazing au pair) and my husband. Have minimal memory of those visits. Apparently I fell asleep mid sentence with Madison and little Roxy was so shocked at how ill I looked, well she was too scared to come and talk to me. I sleep through all of Wednesday and Wednesday evening, only waking to be given more drugs to ease the pain. Why do they wake you...you have a drip in my vein, just get it in there!

Thursday 12th February: Catheter is removed and I am helped to the bathroom, after being given a full bed bath (words can not describe just how wrong it is to have 2 people washing you, whilst making conversation with each other over you), to make pee pee on my own. Big claps all round... I feel like a potty training toddler. Am told I must ring the alarm each time I need to pee so that someone can help me walk, as I am attached to two drips and I have a catheter for internal bleeding which has a bag attached to it. So true to Coleman stubborn form, 20 minutes after they had left my room, I set off to the bathroom on my own. So anyone who has had a c-section ( I did with Roxanne, which helped me tremendously with this op) or any form of stomach procedure, will know how painful the first few days are, you can not walk, you can not pull yourself up, you can not sit up using your stomach muscles alone. Now I have strong stomach muscles, but this was going to be a test to my strength and determination. I figured out a good routine. I raised the head end of my bed and get into a sitting position. I pull "blood bag" over from right side, so that its together with my drips on my left side. Ok, now to shuffle legs over so that they are then over the bed and I pull myself up using the edge of the window and edge of the bed. OH THE F*&KING PAIN IS UNBELIEVABLE but I am there, I am in a standing position. I find walking, well I say walking, more like a slow Michael Jackson moon walk/shuffle, doing that backwards whilst pulling my intravenous drip stand (its on wheels) works well.  It took 35 minutes from bed to bathroom to bed again. I did it. I feel victorious.

Chicken soup, chicken soup, yes yes, please can I have some more chicken soup!!!!!! Seriously, it even came in different size boxes to try and trick me to believe it was something else. I am only allowed to go home if I can poop or fart. Well then, stop giving me chicken soup and something a little more encouraging so that my newly reformed plumbing will get excited and give you the results you want!

Sunday 15th February: I am allowed to go home. Got a big hug from lovely surgeon man and told I have done very well and all seems ok, he had good look around inside and there are no signs of the Trevor spreading to other organs. Phew. I just need to be at home for a couple of weeks to recuperate and I'll be good to go. Appointment booked to see lovely surgeon next week for check up and to remove the minimal stitches that I have.

Wow, I am exhausted. Totally wiped out. Simple tasks as getting up to have breakfast with my girls is totally debilitating. It is so important for me that my girls see me each day making an effort, being strong. I have a routine. I wake, I have breakfast with them, I go back to bed. I wake at 1130am to prepare lunch and am with them until they leave for school again at 2.30pm then back to the sofa or bed. Thank goodness for my amazing au pair.

Wednesday 18th February: Lovely surgeon gets his second WTF reaction to his announcement that Trevor was very aggressive and cancer is in some of my lymph nodes. Chemotherapy is required. I have to leave the room as I can feel the tears burning my eyes. I find a bathroom near to his office and have a very large WAAAAAA moment, wipe my tears away and head back to lovely surgeon's office. He has a fantastic manor about him, very reassuring but I am still struggling to take on board what he is telling me.  Appointment is made to see oncology the following week. Chris and I leave the office, tight hand hold and walk to the car. We decide that we must tell Madison. How do you tell your eldest child that Mummy has cancer and will need treatment that will in turn make her ill but eventually make her better. How do you do that...that is not written in the "how to be a parent book" that they give you at the hospital when you come home with your new precious child. Oh yes, that book that does not exist!!!

To see your first born hurting, scared, crying is something that will remain with me forever. Madison is such a strong girl, full of love and life. I momentarily tore her secure world apart...we explained that I will get better, her reply "you can not guarantee that though can you, Daddy told me that they had removed the bad piece and that you would be better" How do I answer that? I cry for her that night.

Week commencing 23rd February is full of anxious hospital visits. I will require fortnightly chemotherapy of Folfox 5FU (seriously, my treatment sounds like a 1980s sci fi series!!) and this will last for 6 months. I will have 3 hours at the clinic with chemo then home with a chemo pack attached to my port a cath for another 48 hours. They do not give you much information here, the bare minimum and I'm guessing that is to not stress you too much. Port a cath is also fitted, this was the defining moment for me, when I suddenly realised and accepted that I HAVE COLON CANCER STAGE III.  I felt broken when this was fitted. The invasion in my body, the realisation that this was gong to be my toughest work out yet. This week was full of highs/lows, unexpected waves of tears. The tears come involuntary and completely take hold of my body, they only last for about 30/40 seconds and then I am fine again. It feels like grief, I feel grief for the stress and upset this is causing my family and friends and I have no control over it. I need to have control over this. Thankfully, I have an amazing support network here, people to just be here if I need to talk and to laugh with. I have been showered with love, gifts, flowers, lunches and it really does make a difference knowing that people love and care for you.

Chemotherapy can only start after the 4th week of surgery and mine will be four weeks to the day. My chemo starts on Wednesday 11th March at 1645.

"The best protection any woman can have ... is courage" ~ Elizabeth Candy Stanton