Showing posts with label secondaries. Show all posts
Showing posts with label secondaries. Show all posts

Monday, 19 October 2015

Last Chemo Tomorrow!

My last Chemo is tomorrow!  

What a momentous occasion!  I am so excited, not because any lingering cancer cells will have been killed off by the end of this treatment, nope, I am excited because I won't have to go through side effects again and a bit of normality will return.  Oh my good God what a relief that will be. To counter my unbounding joy at this, I have got a year of Herceptin injections ahead and we don't know yet what the side effects of that will be as the two injections I've had, have been at the same time as Chemo. 

But I am choosing to ignore that, I've decided that it won't affect me at all. So back to the positive stuff.

I can't wait to feel normal again (what is normal? My normal!).  No more feeling yuckety yuck.  Plus plus plus....My hair will start to grow.  I can't wait to have hair again.  I will never diss my thin lacklustre locks again! I want hair!!  Any will do.  It will be whatever colour comes through, mouse with grey I think.  I've not seen my own colour since I was 14 when me and Karen Harris started splashing lightening setting lotion on our heads!  No such thing as home highlight kits then!!  So mouse grey will do.  It may also grow back curly, so grey afro here we come!  They say it may come back thicker which would be amazing, but I'm not greedy, thin and scraggy will do!!!!  Eyelashes too!  I've missed my eyelashes!  How daft is that? When I rub my eyes it just feels wrong.  I miss putting on mascara.  I've got false lashes but it's really hard to put them on without an existing line of lashes to guide you.  My eyebrows were never thick, a youth spent overplucking to blame for that,  but to have a complete line would be lovely.  As for hairy annoying legs, armpits, moustache, chin, nose, lady bits, well you can keep all that! That's been the one and only good thing!!!!  I should have been listing all the yuck stuff that happens and saying I'm so glad this is the last time for all of that, but just take that as read.  I'm just excited about hair!!!  Am I shallow?  I think I must be.  But who cares?!!  Just give me hair!!  My nails are another matter, I think they may take longer.  They are currently starting to show signs of distress and it may take a good few months for it to grow out, so I'm ignoring them for now.

Apart from the shallow stuff above, I also can't wait to go out. Out anywhere!  Because my immune system drops down to nothing on this second drug regime, I took the decision (mine not Docs) not to risk mixing with people and picking up infections.  I have injections for 8 days after the Chemo to help boost my count back up, so why would I want to undo all the good I've done?  So apart from the hospital, I have been nowhere.  After this next lot of side effects are done, in three or four weeks time or so, I'm going shopping!  I'm going to stand in the city centre and see more people than I have done for God knows how long and I'm going out for a meal and I'm going into the office.  Freedom!!!!

Just slowly and gently, I'm not going to go crazy, I need to build my body back up. I feel like a gorilla born in captivity that they slowly reintroduce to the wild!!!

So it's hair, shops, meals, work (yes sadly).

I can not wait.


Sunday, 18 October 2015

Doing Daft Things for Cancer Research

Oh my! My rather gorgeous nephew Samuel Wilson is doing some fundraising. He is doing mad stuff and you can watch it online (don't ask me how, I'm over 35). He is doing this in memory of his Grandad and to support me!! Am rather overwhelmed by this. So good people, please support and donate if you wish. It's for Cancer Research!



 https://www.justgiving.com/SoItsMaestro/



Sunday, 11 October 2015

Bravery


I never understood why people described cancer sufferers as being brave.  I just didn't get it.  Surely being brave is jumping in a river to save a drowning soul, or defending your military position against certain death, or standing up to bullies in the face of actual pain and humiliation.  That's bravery surely?


Yet cancer sufferers are paraded across our TV screens and newspapers like gods we should worship.  With all the accompanying wordy waffle of the feats of their bravery.  I couldn't understand what bravery had to do with it.  If you've got to have some medicine to fix you, that decision isn't brave, it's just foolhardy to refuse!


Apart from kids.  A photo of a bald headed little kid with a tube up its nose and an IV drip and trolley being dragged along, would of course elicit only sympathetic words like "Brave little thing" from me.  I don't know why I discriminated between children and adults.  Perhaps I saw the children as innocent and maybe viewed the adults had caused their own downfall in some way? (A discussion for another day).


Now that I have a Breast Cancer diagnosis I do feel a little differently about the "Brave" word.  I still don't think it's a good fit.  I think "Coping well" or "Handling it" or "Getting on with it" are better descriptors.  But I do admit to feeling that I may be a little bit brave at some points.  This is usually just before a Chemotherapy session.  I really, really don't want to do it.  My body has just started to heal after the last poisoning session and I am fully aware of what is about to happen to my body all over again and I quite simply do not want to do it.  Yet to me it is more of a question of survival than bravery.  Survival comes top of this particular decision making criteria.  (Anti chemotherapy souls may dispute my survival theory here).


But with all this unsolicited experience to my name, I am, whether I want to or not, expanding my comprehension of bravery.  I get it now that those dealing with illness face challenges which are met head on with stoicism, pluckiness and fearlessness.  That is their brave decision.  They could decide to deal with it by complaining, moaning, making a fuss, blaming medical staff for pain and turning against their loved ones.  Yet to remain resolutely defiant that you will not be brought down by this mass of unfair circumstances is most definitely a brave decision.


So I take it all back, my easy dismissal of yet another brave cancer victim.  Anyone who can sit and watch that chemotherapy liquid infusing into their body with the full knowledge of what will follow, is most definitely brave beyond words.


So there, I'm brave.  So are many ladies including Juliet, Marion, Karen and Tracy. Here's to us. (Plus all those before and those that will follow, too many).


I also have to include a mention for the Kidney people out there, both dialysis and donor. Jackie, David, Ruthie and Gaz. Wow.


Brave people xx


One favour, please do not comment saying I'm brave, my detractors will say I have only written this to get "brave" comments. It's not been done for that reason, it's a simple discussion on what "brave" means to me. So no brave comments!!!! Thank you x

Thursday, 8 October 2015

A Welcome Side Effect Would Be....


I've never been a skinny shape
When 7 stone there was no gape
Around my thighs jeans stretched tight
Against the wobble there was always a fight
I yearned to have long lean pins
Managed only half decent short shins
The trauma and worry of a big fat bum
For a seventies teenager was no real fun
Not conforming to a skinny size
My bum and hips I tried to disguise
My one saving grace
Was my tiny young waist
But straight up and down I did not go
Curves in those days a big no no
A tendency to spread was the norm
Child bearing hips always the form
If only Kardashians were popular back then
On the Bo Derek scale I would have been Ten
But that's how it is, just the same for us all
The more we want skinny, the fatter we fall
Age increases size, weight keeps track
But it's not so bad just look at my rack!
My bosom happily detracts the eye
With a whimper and sometimes a sigh
From looking at my rolling spare tyre
I can't deceive, my belt's not a liar
There is no excuse, I'm aware of that
I could eat less, do more and not get fat
But wait what's this? At last there's a chance!
A bad ass illness could just be the lance
To burst fat's hold on my wobbling bits
And lighten the load on my so heavy tits
My boobs big and bouncy have attracted a fight
The way I see it with a glimmer of light
It's bad, mad and wrong to look with such glee
At what side effects might just do for me
But if I go through a real rough time
At least the scales could come under nine?
I really am looking at this in a positive way
Onwards and upwards to a skinnier day.
The treatment is tough and there's no guarantee
I may win, I may lose, we sit wait and see
But my fingers are crossed I might get thin
With everything else surely this I can win?


What? Wait, I'm not sure I hear what you're saying?
I'm going to have to start seriously praying?
No don't bring me down it can't be true
The opposite can happen? Who can I sue?
You're telling me I will soon start to crave
Foods full of comfort, they'll all be my fave
Too tired to chew?
Pop a sweetie or two
No energy to crunch?
Have a soft carb lunch
Tummy won't do digestion?
Sugary drink's a suggestion
Taste buds receded?
Bread freshly so kneaded
A mouth so dry you can't swallow?
Fresh sorbet with ice cream to follow
Those meds and steroids are messing my brain
My reason and logic is starting to drain
They definitely told me some people lose weight
So why is Humpty Dumpty my inevitable fate?

From all the side effects, one may just have been
A nice new look, trim slim and so lean
But it's not going to happen, I will have to agree
Easy popping carbs offer comfort for me
A quick energy fix is first and foremost
So vital to help the counting cells boast
I simply can't worry about things expanding
There's time ahead to be more demanding
Day by day I'll eat what is right for me
And adjust my clothes to easy and free
But honestly, really, why couldn't it be?
That Chemo slimmed down podgy old me?

Sunday, 4 October 2015

Going Public



We are a strange lot us human beings. Thankfully we are programmed quite strongly to help each other with survival. However underneath that we have multi faceted layers of complicated feelings, worries and anxieties. So many what if's, I'm not sure’s and what will they think’s? We are all going to react to major circumstances in our lives in many varied ways. These reactions may serve us well or they may result in more devastating problems. We just don't know. All we can do is go with the reaction that feels right for us. Only time will give us the clarity of hindsight. During my current progress through the web of illness recovery, I have discovered that we are all a little fond, myself included, of a subtle criticism of the way people deal with their illness. I understand this is a basic human response, as we want to validate our own choice of action as being the right one. The problem I have found with this, is that while it helps to strengthen your own resolve, it fairly well decimates the person you are criticising. I have chosen to go all out and tell everyone everything. Others tell no one but their closest loved ones. There is a whole range of individual and unique reactions, from those who go over the top and leap on the "Illness" train, with a need for attention that makes you cringe, to those that stay so quiet, sheltered and reserved that they become resentful that no one understands what they are going through, because no one knows. It is such a difficult balance between dignity and ignominy. That balance will only be chosen by the person viewing you. You have no control over the way they see you. We may feel so passionately that someone is making such a wrong choice in their life and feel there is nothing ahead for them but impending doom. We may have tried to explain this to them, yet they dismiss our concerns and assure us they know what they are doing. Hopefully what we do is sit by, watch and be ready to pick up any pieces should the worse happen, without ever saying those awful words "told you so". But if we end up wrong and everything goes right, can we say "I'm sorry, I was wrong". I'm not sure we can! Everyone has valid good reasons for behaving how they do, even if they can't elucidate why, it just feels the right thing to do. When I was first diagnosed, I took some time to decide how to deal with it. There is so much to consider apart from all the medical facts and the practical problems, but the biggest worry is other people. It is so easy to upset them. I know that sounds mad and should be the last thing you worry about, but for me it was one of the first things. I had to somehow balance my feelings and needs with theirs. I've always been happy in my own company but I do love knowing I have the support of my family and friends, without that I'd feel very isolated. I don't want to be mobbed by people, that would drive me nuts, but I am very very fortunate in knowing I could turn to any of them and say "help". That means the world to me. So my decision to go public about my breast cancer was, of course, multi faceted. Firstly laziness came into it. Trying to keep everyone updated was going to be much easier done all in one place! Secondly, I hate awkwardness, I dreaded meeting someone and having one of those conversations where we dart around the subject that no one will broach, yuck. I'm much happier when someone says "how are you?" and I reply "shit" and we move on. Love it. My next reason was one I am very passionate about and it's now become a clichéd word "Awareness". I feel compelled to tell people to check their boobs. Following on from that is my need to help others, whether they are diagnosed or are supporting loved ones. To me knowledge and understanding are so important. Sharing a recovery journey is one of the most important coping mechanisms for me. Hearing that someone has a similar side effect, reduces your anxiety levels. Comfort in numbers. Lastly I love writing, always have done. I have that need to be creative and lying in bed tapping my keyboard gives me such a wonderful release. I did try crochet (which I love) but it was too much physical effort! In truth I would be stifled without this wordy therapy.

I'm aware that I sound like I'm justifying my actions and that's not what I want this to be about. I want us all to be aware that other people's choices are just that, other people's choices. We must try hard not to take slight or be hurt by them. We must put our feelings second to those of our friend or loved one and do our best to support them through their choice. It's a big ask I know. Because underneath it all, we just love to be a little bit bitchy, don't we?!!

So read it, don't read it, criticise me, praise me, share my words, delete my words, understand me, ignore me. It's your choice and I respect it. I'm just happy doing my thing and very much hope that by doing that no one feels I am criticising them!

Complicated darn world!!

Saturday, 22 August 2015

Chemo and Daytime TV


Halfway through my chemotherapy
And I haven't once watched Jeremy
Even with all this time on my hands
I refuse to succumb to TV demands
Daytime TV is no place for me
I'd rather set my imagination free
So my brain wanders from place to place
Improving my lot is not a fast race
I'm slowly marching through each week
Obviously without being too meek
I've dealt with the first three infusions
How nice if the next three were just illusions
The therapy now changes, it's all anew
Side effects will come out of the blue
The unknown is what causes most concern
But from a path travelled once I will learn
What helps, what hinders, what will heal
Only then can I wholeheartedly feel
With true judgment and cunning wile
I still don't want to watch Mr Kyle!







Thursday, 20 August 2015

Look for Lumps = Look for Life

Be honest ladies, how many of you have run your fingers over what felt like a lump, had a mini electric shock of fear course through you, then hurriedly move your fingers away and ignored what you may have just found?  

My hands are up, I've done it in the past!  My boobs are naturally lumpy anyway and whenever docs and nurses had a rummage in them, they always found something, but it was always a harmless natural lumpiness.  Anything that I found I always put down to that too. I quite simply sectioned it off to those compartments that us girls have in our heads, that are titled "nothing to be worried about". We don't want to make a fuss and take up the time of NHS staff for simply nothing. But that really isn't the right attitude nowadays.  

I bet you will know not only 1 person with Breast Cancer, but more likely at least 2 or 3 if not more.  You may even know people that have passed away from it.  It does seem to be everywhere now.

Thankfully when I felt my lump, I just knew it was a nasty one.  It felt different.  But I did have that fleeting moment of thinking "Ignore it", seriously I did!  Luckily that disappeared from my brain in a nanosecond.  But what if it hadn't?  What if I had ignored it?  Not wanted to make a fuss, not wanted to go through the awful waiting for results? The period of keeping it quiet in case it was nothing and I looked a fool for making a song and dance over nothing? Quite simply, my lump would have grown and spread, I would be looking at a very different scenario than the one presently before me.  

Once you can feel a lump it has the ability to spread, this means you have to leap into action, not sit around pondering whether to do anything about it!   Did you watch "The C-Word" recently on BBC1?  It was raw watching for me as I had only just been diagnosed, but a Mammographer that I know, reported an increase of 30 women who, following the programme, noticed changes in their boobs and followed it up, 3 of those women were diagnosed with Breast Cancer.  That was just in one hospital in one town.  Potentially that one programme has saved 100's of lives.

So you see if you find it early enough and follow it up, you may well save your life!  We have to accept that Breast Cancer is out there and its likely to get you, so let's stop it in its tracks!

I want looking for lumps not to be equated with a dire outcome, but a positive one, looking for lumps should equal looking for life.  Go looking for lumps, understand your boobs, know their road map, know how they feel throughout your cycle, you will then stand a good chance of feeling any changes and acting upon them straight away, look for life.  Impress on your daughters and granddaughters that this should become a habit for life.  I support the Coppafeel charity because they start with the youngsters, they offer a free checking reminder service. Take up that service whatever age you are.  Lets make lump finding a positive thing. Please also remember it's not just lumps, but any other changes too.  Get to know your boobs!



Monday, 17 August 2015

I've had the results of my scans

I've had the results of my scans......

We had been fairly petrified of what we were going to hear, a bad result meant we could be given a scenario of how many years I had left, but praise the Lord and hallelujah, the results were, no secondaries! This means my cancer has been contained, so my surgery and chemo etc should all be effective at knocking it on the head! (We will need to wait until treatment is finished for those results). So at this moment, after the scan results, I am very grateful and much relieved!

But....

I have to say "But". Why? Not because I am the most negative, pessimistic soul ever, but because I am a realist. I like to have all my facts and figures, know what the reality is, decide on my course of action. I also say "But" because I need to look after everyone around me. I need to be careful with their emotions and feelings. I care for them because they care for me. If after my treatment, I was to say I'm "all clear" they will quite rightly rejoice and feel relieved!! However if after 1 year, 5 years or 10 years, my cancer comes back, they may think, she told me she was all clear, what has she done to herself? Did she not look after herself? Didn't she do all the correct things she was supposed to do? I know they may think this, because I've thought it myself of other people. Have you not been a little bewildered by people you've known who have gone through all the chemo etc and said they've beaten it, but a year or so later it returned? I was. I now know that it comes from a complete lack of understanding of how breast cancer behaves, or rather misbehaves! This is how it goes, the surgery, chemo and radiotherapy should kill off anything that exists. The hormone and targeted therapies will help to reduce the risk of recurrence. So BC can then just decide to pop up again either as a repeat of the first time or as secondaries in other parts of the body. This is where my "But" comes in, I know my statistics, I am aware. I have less chance of recurrence than someone who smokes dying prematurely, 50% of smokers will. Most smokers live in a dream world of denial. I'm not in denial. If cancer dares to strike me again in the future, I will be prepared. If I told people it was beaten and then it came back, how puzzled and mystified would they feel? I have accepted, that albeit in the low percentages of chance, there is a possibility it could return, the rate is approx 25%. (To all smokers out there, look at me and realise that I have a better chance of living longer than you!!! That might make you give up!!). The recurrence rate is roughly the same for all Breast Cancer club members. It's the only cancer where you can't say after five years it's all clear, because it can come back after even 20 years! You can however, say that your cancer has been treated. Treated and cured, I have learned, are two different things. Now please believe me when I say I am incredibly positive and I am not being negative in any way, I am just being realistic. I have a future. A future filled with laughter and love, my future. What this future will have to contain though is for any lumps, bumps, aches or pains that arise, I will have to view them with a little more suspicion. Now trust me, I can handle that! The answer I will be looking for is, there is nothing wrong. I will not be spending my life thinking it may be cancer, now that is negative! However it is a conundrum, looking for lumps and aches all the time is negative, but ignoring them is negative! What's the one thing that we are all persistently told? Examine yourself, get it checked out. So why then after a diagnosis would you not follow that advice? It is the most positive action ever. I've saved my life once already by finding my lump in time, I'm definitely up for saving it again should those pesky blighters dare to return!! I believe taking a pro-active stance is positive. This can't be viewed as having a negative outlook. So when I say I have "no secondaries...But" you now know that it's a positive thing to say "But", it will help those around me to deal with possible future shock and most importantly, it may well just save my life! Again.