Reality hits and it hurts

3 minute read time.

I pride myself on being a positive person and have tried to be positive so far during this time.  Let's be honest my prognosis is good compared with many others and whilst I have a difficult journey ahead I have hope and that is really good!

However, this is not going to be a positive post, there was bound to be one which snuck in.  This weekend I have been miserable.  

I was so positive on Friday, I was feeling so good after my second chemo.  I am on a treatment plan where I have taxol (Paclitaxel to use it's full name) weekly and then the other drugs as well as taxol every three weeks.  Last Thursday was a Taxol only day so it was a shorter session and on Friday I felt chipper and almost normal.  I managed a walk in the sunshine and stayed up beyond 9pm! 

Saturday morning came and again I felt great so I thought perfect I will do a very normal thing and do a bit of light housework.  Big mistake!  After merely tidying the boys rooms, hoovering and sorting the living room I was absolutely shattered and it took it out of me for the rest of the day.  I was so mad at myself the good feeling I woke up with had disappeared. I had to sit down for 45 minutes before I had enough energy to help decorate the Christmas tree with the boys.

What's more Sunday came around and I have never felt like I had less energy.  Was I being punished for daring to think I could do anything for myself!? It felt like it. I had to retreat to my bed for a rest without having actually done anything.  We did manage to get out for a family walk which was lovely but that was as much as I could muster.

Normally with a couple of weekends before Christmas I would be full of Christmas cheer, drinking in the Christmas spirit and dragging the boys here there and everywhere to do lots of festive activities.  I suppose, silver lining, thanks to COVID, many activities are not on at the moment so at least I am not missing out on much but I feel like I am missing my Christmas spirit.  I've written all my cards, bought all the presents and decorated the house but just don't feel like it is Christmas yet.  I have barely sung a Christmas carol or watched a Christmas service, I just feel like it's Christmas for everyone else and we happen to have a tree in the house?

I tried to keep a happy face on yesterday for the boys, I don't want to pretend for them but I also don't want to spoil their Christmas.  They are getting so excited and it's lovely to see, I just wish my usual excitement was there with them! 

With speed from diagnosis to treatment I still haven't had a chance for my brain to catch up on how this is all really going to take a toll on me and my body.  I wasn't stupid I knew I would be tired and I wouldn't be able to do everything as I had. But I wasn't prepared for the sheer up and downs, the feeling so perky one day and utterly devoid of energy the next.  I hope I will get used to the contrast and learn how to manage it better.  I also hope that my positivity returns.  I am feeling better today.  I'm back at work, having some focus is a godsend.  Fingers crossed the positive Christmas spirit will hit me in the next couple of days! 

In the meantime, take care everyone xx

Anonymous
  • I know what you mean about Christmas feeling a bit hollow this year (like looking at it through a window rather than really feeling 'present' in it). I think a lot of that comes because of the weird COVID year we've had, it must be exponentially more difficult when you're coping with a recent diagnosis and rapid shift into treatment. There is no doubt about it - this Christmas is going to be a very different one, so don't even try and compare it to others, you need to take care of yourself, and that might mean sitting in the sun watching the kids rather than racing around with them, so tough to do when you're used to being so active, but this too shall pass, imagine what next year might bring. Sending lots of love. A

  • 14th December was my first Chemo day, As the hospital had stopped the cold cap facility due to covid 19 I bought my own from Amazon recommended by Doctors cost around £100, however, as I needed to have a bone scan prior to that, the frozen gel sachets melted, so I could not use it. The Chemo nurse was really good, she shared her own experience of breast cancer and put me at ease, however, I was scared once I saw all the 6 syringes 60ml 3 red and 3 clear, I cannot remember the names, plus other items given. I sweated bad that night, but temp only went down to 36.1 called Chemo team they were ok with that, if it went below. That week I was Nauseous and dizzy, fatigued. second week, I seem to pick and was able to do office work from home in small intervals, now the third week I have a purple tongue and a bitter taste in my mouth. I have lost all my hair, it was everywhere, so I shaved the last few strands here and there off. my next treatment is on 5th Jan and I am not looking forward to it. I suffer from insomnia like your self, and my brain is always on.....yesterday I was drained and today like yourself I feel more energetic. 

  • Also, I was told that as I have more treatments, the Chemo accumulates and I will feel more fatigued and weaker, this does not make me feel good.

  • Sorry you’ve felt so fatigued as well. I’ve had five weekly treatments now. And whilst it is cumulative I would say my body has adapted to how to deal with it in a way. So whilst I’m more tired I know better what I can cope with if that makes sense? All the best for your treatment this week, take care xx