Thursday 23 April 2015

The Sun is Shining


Well seeing as the last post got a bit emotional and deep, I thought I'd just share some of the good stuff I get up to during my good days off chemo.

After a round of chemo, I generally get roughly a week of feeling just about normal, a little bit of muscular pain, mostly in my shoulders and back (maybe from being laid up initially?) and a bit fatigued but, I manage to get about and live a bit of a life. I'm trying to fill my well days with positive and happy activities, that way hopefully the bad days speed by.

Luckily, the weather is getting better which means I'm managing to get out a bit with the dog. No where special, just our local park, but there's a lot to be said for simply getting yourself out for a walk. The act of putting one foot in front of another really seems to have the most amazing effect on my mood. It is hard work, I get tired and breathless, but there's plenty of benches for me to have a sit and recover on. I've long said exercise is a very under utilised anti-depressant!




Happy as a pig in muck

A little slice of heaven
What's life without a bit of what you fancy? I came across this Nutella Mug Cake recipe online....rather dangerous if you ask me, cake in literally 5 minutes.


I made if even naughtier by adding extra thick cream on top. I must be the only cancer patient to put on weight! Better start watching what I eat!

Monday 20 April 2015

The Joys of Chemo Part 2


The thing is with chemo, it doesn't matter what the doctors tell you, it doesn't matter what I write here, no one can ever tell you how it will feel. Sure, the doctors can tell you to expect nausea, fatigue...tired. But what do those words actually mean? As someone who was reasonably fit and healthy before all this, all I can say is, the doctors have made me feel crappy. The logical side of me knows that this is all temporary and it's for the best, but that doesn't get me through the horrendous heart burn, being too tired and weak to even get myself a cup of tea or the feeling of being completely and utterly useless.

You see, as someone who has worked hard all my life to get to where I wanted to be, to suddenly feel useless takes some getting used to. I'm sure my loved ones will tell me I'm being ridiculous, but I feel pathetic. I want to get up and go for a run (one of my most loathed hobbies, might I add), I want to cook dinner, I want to have the appetite to eat my dinner. Really, I'm just feeling rather sorry for myself at the moment and that does not sit particularly easily for me. I know it's preposterous, but I feel like I'm letting my loved ones down, but more than that, I feel like I'm letting myself down.

Never in my life have I let an obstacle get in my way, each set of exams or hardships in my life was just another conundrum to be figured out and worked around. Except now, now I feel like I'm languishing in a sort of "no man's land". My career is adrift for the next few months, my life plans are at the mercy of my doctors and I feel like I'm just wishing away the next year or so of my life. I wish I could say this diagnosis has made me a better person or more positive. Perhaps in time, it might and teach me to live life to the full. But if I said that now, I'd be lying. In the deepest recesses of my mind, if I allow my mind to wander too much then there's fear, an overwhelming, crippling kind of fear that paralyses me and makes me weep. I fear for my future, my health, but most of all I fear for my loved ones. Dying is easy. It's the ones left behind that have to pick up the pieces and carry on. I worry for my husband, I worry how my parents would cope. Of course, I am not terminal and I know I'm in a far, far better position than most. But still, if I allow it, the fear creeps in.

When I was first diagnosed, my husband (still feels weird saying "husband". James and I have been together 7 years now, but only tied the knot July 2014) and I were referred to a psychologist. One of the issues identified is the worrier in me. I worried about everyone. I worried about James going on the motorway to work - even though this a journey I took myself, almost on a daily basis. But I worried about him getting into an accident, but I never once thought of myself being hurt. I worry incessantly about everyone I care about. Yet, it was me to get sick. It was me that would cause everyone to worry. Anyway, from this my psychologist wanted me to explore "mindfulness". Essentially, a way of pushing away my dark thoughts. After all, just because my mind goes to dark places, does not mean it will happen.  Funnily enough, I recently saw an article in the daily mail about the "mindfulness diet". Something about being aware of what you're putting in your mouth and never having to diet again. Not sure what my psychologist would say about that really.

So here it is, if you got to the end of my rather long winded, waffly and let's face it self indulgent post; thank you. Maybe I'll even give this whole mindfulness thing a go and see if I never need to diet again - I mean change my way of thinking so I don't worry so much anymore.

Incidentally, today is Monday Cry-day. It's my first day off steroids after my FOLFOX infusion and I always find something silly to have a weep over - last week it was because the steroids were making my face puffy, this week I let the dark thoughts tumble out in a cacophony of tears and rather attractive snorting over the telephone to my poor mother. So let's the this post with a little bit of positivity, here's a rather nice car selfie, taken on my way to a genetics appointment (more on that later) and one of my beloved pooch Alfie.




My husband hates all my selfies, he thinks they're attention seeking and he seems to think I'm too social on social media. Stuff him I say! When you're feeling rubbish, a girl should capture when she looks good! 

Friday 17 April 2015

The Joys of Chemo

Cycle 5 Chemo Selfie

So, my surgery went really well and they got clear margins around the cancer, so I'm having chemo to make sure no sneaky cancer cells made their way into my lungs and liver. There was nothing to suggest this on my scans, but sometimes the cells are too small to pick up on scans.

My doctors have me on the FOLFOX regimen which is three different drugs, every fortnight I go to the chemo unit and have an infusion which lasts 2 hours and then I go home with a pump full of Fluorouracil which lasts a further 36 hours.

36 hour Fluorouracil Infusion
I just had Cycle 5 yesterday and I'm feeling pretty sleepy. First few days after chemo is pretty hard work. I'm very tired, sickly and generally a bit miserable. Luckily, this only lasts a couple of days and I get roughly a week of feeling myself and I can get out and about before the next round. I suffer quite a bit with peripheral neuropathy, basically any cold stimulus to my hands or feet sets of intense pins and needles and I can't drink any cold drinks because it causes my throat to go into spasm. Cold air tends to do the same with my throat. 

You know the worse thing? When you're told you can't have something you just want it so much more! So here I am craving orange juice! Roll on August (last round of chemo is due July 23rd) when I can have ice cream!!

Thursday 16 April 2015

The first post and the Story so far

Hello and welcome to my blog, lemme quickly catch you up.

November 2014 - Diagnosed with Stage IIIA rectal cancer
December 2014 - Surgery to remove roughly a third of my bowel (Abdomino-perineal resection with permanent colostomy - 2 lymph nodes positive for cancer, but clear margins)
January 2015 - Emergency IVF cycle for fertility preservation - one embryo frozen
February 2015 - Started 12 cycles of chemotherapy, due to end July 2015

So that's pretty much it in a nut shell, pretty rubbish news and pretty rubbish couple of months, but I have my dog and my amazing husband and friends to keep me smiling.

Keep reading to follow me on my journey!