Pages

Tuesday 26 April 2016

Maintenance: the Good, the Bad & the Ugly

I'm currently on my final, longest, and least aggressive phase of chemotherapy treatment for ALL, which is called maintenance. 

What Is It? 

I started maintenance treatment in January 2014. For boys, this phase lasts 2 years and 7 months, and for girls it lasts 1 year and 7 months. 
Because I'm on a clinical trial, my treatment isn't the same as patients who were randomised to other experimental conditions. For me, maintenance treatment means the following: 

  • Oral chemotherapy every evening
  • Additional oral chemotherapy once a week
  • IV infusion of chemotherapy once a month
  • 5-day block of steroids every month
  • Intrathecal chemotherapy every 12 weeks
However, some people on the trial get randomised to not receiving the latter three. 
The purpose of maintenance treatment is mostly preventative care; most of the leukaemia cells are killed in the intensive stages of treatment, and this is mostly to make sure they stay that way. 

The Good

Maintenance treatment is a lot easier on the body than the intensive stages. People will be put on different doses of treatment but in general, all of the side effects of the chemo slowly get a bit better and more manageable. Your hair grows back and the sickness and nausea aren't as incessant. 

As well as the meds getting more manageable, so are the hospital visits. I still need to go in for chemo, clinic and blood tests (fun fact: Google Maps has automatically marked the hospital as my "place of work") but this has gone from being nearly ever day to about every other week, which means hospital visits aren't running my life as much any more. 

Both of these mean that you can do more. This differs from person to person, depending on their situation, but I myself have been able to take on some voluntary work which I wouldn't have been able to do beforehand. Because my immune system is a bit stronger, I'm able to go on short breaks away and more social events, as well as a lot more freedom with what I can eat! 

A lot of the opportunities offered by cancer charities aren't suitable for patients on the intensive phases of ALL treatment, but maintenance gives you that bit more flexibility to take part in them. For example, you can see some of the stuff I've been up to with Teens Unite here

The Bad & The Ugly

One of the common complaints I hear amongst my ALL friends is that "people assume you're okay now, but you're not".

Basically, maintenance makes me feel like I've got a constant hangover. I can have the best night's sleep ever and still wake up feeling tired and drained of energy. This is something I have got a little accustomed to over time, but it still takes its toll. I often find I can't join in with things which are early in the morning or late in the evening, as I will be too fatigued, which goes against the grain of a 21-year-old's ideal social life. 

Most of the side effects are pretty manageable, and nothing I should complain about, but they are all still there. I spoke previously about how my hair is thin and falls out easily, and nausea and vomiting will affect me about once a month. Because my immune system is still pretty poor, I'm more susceptible to things like colds and infections, which hit me harder than they would a normal person. As I said, they're nothing I should complain about, but I still have unpredictable "bad days", which (in conjunction with day-long hospital visits) means that at the moment I couldn't even consider getting a part-time job. 

It was at the maintenance stage that I realised the longer-term implications of cancer. As many of you know, my steroids had to be stopped because of avascular necrosis in my ankles. This means that, in the past year, I have had to give up running and my gym membership: two things which I loved doing and really helped with my mental and physical wellbeing. (I've been struggling to find forms of exercise which I'm physically able to do, and am currently trying to give swimming a try, so fingers crossed!)

The most frustrating thing I've found with maintenance treatment is that I try to fit in to normal life again - the life that my school friends and other people my age are living - and find I'm not able to, or I don't fit in any more because I've been sat in hospital not doing anything for a few years whilst everybody else has been moving forward, which is unbelievably disheartening. 

Many patients, myself being one of them, enter maintenance and "try to run before they can walk". I've found this applies to most aspects of life: social, fitness, romance, work, etc. - like you're running through mud and getting nowhere fast.

Finally... 

Despite the good, the bad and the ugly, maintenance is something which I try my best to just get on with, and haven't really spoken (or moaned) about much until now. Of course, I have much to be thankful for, I guess I just wanted to put across the whole picture and both sides of the stage which I am at right now. 

As always, a reminder that everybody's experience of cancer is different, and I have seen so many different experiences of people going through maintenance. This is just about my own experiences! 

Feel free to add a comment or question below, or fill out the contact form!

Thanks for reading 

Pete

Wednesday 20 April 2016

Before The Buzz




I can't believe how quickly my fundraising target for my headshave was smashed! A big thank you to everybody for your kind and generous donations.

As I mentioned in my last post, I have brought plans to shave my head for charity forward, and I set myself the fundraising target of £170, which would cover the cost of the initial care grant given out by CLIC Sargent at diagnosis. Within a day, this target was smashed, and currently stands at £260! (See JustGiving page here).

£230 could fund for a family to stay in a CLIC Sargent Home From Home for a week, as my family did (but I'll probably post more about that later) - so this is an amazing amount! I wanted to write this post to give some details, before the buzz...

I originally wanted this to coincide with another fundraiser which I am working on and will be announcing soon, but I wanted to move it forward, before my hair is too thin to donate!

This is why I didn't set myself a really high fundraising target for my Big Buzz - I didn't want to be haggling people for sponsorship just before asking them to support my next fundraiser - which is something I'd really like a lot of people to get involved in!

I haven't made plans for the actual headshave - which is in just under two weeks time - but rest assured, I will be posting a video of it happening, and lots of photos, so watch this space.

As I said before, I will be donating my cut hair to Little Princess Trust. Due to the chemo, dye and everything else I have subjected my poor hair to, I'm not sure that it will be good enough quality to be made into a real hair wig, but it's certainly long enough and I can but try!

If anybody would like to donate to help smash my target even further, here is my JustGiving page: justgiving.com/petebigbuzz

Thanks for reading!

Pete

Monday 4 April 2016

Hair

I wasn't planning on doing this so early, but my chemo dosage has just been increased again, so here we go!  

My hair - December 2015
For the past 18 months or so, I have been growing out my hair, and now have a man-bun which is several inches long. There are a couple of reasons for this, the first, but least prominent, being me experimenting hairstyles as I have been since the beginning of secondary school. More importantly, due to still being on chemotherapy, my hair is very thin, so I wanted to grow it long to create the illusion of thickness (you could see my scalp through my hair when it was shorter). 


However, the most important reason is that I have been planning on shaving it off all along


On the 3rd May, I will be taking on The Big Buzz for CLIC Sargent and shaving my head back to the wood to raise money for children and young people with cancer, and their families. 

My LPT wig - October 2013
The reason for the growth is that my hair is now over 7 inches long, I can donate my cut hair to Little Princess Trust, to be made in to a wig for a young person who has lost their hair. LPT provided me with an amazing acrylic wig whilst I was going through the intensive stage of my treatment, so it would be great to give something back to them, and maybe help another young person... provided my hair is good enough quality! 



The dosage of my chemo tablets has just been increased again, as per the protocol. This isn't a problem for me, but every time the dosage is increased, my hair weakens, gets thinner and molts easier, so I've brought the date of my Big Buzz forward. 

My fundraising goal for this challenge is £170, which would fund an initial CLIC Sargent grant, which is given to a young person within the first 72 hours of a cancer diagnosis. This is to help with the initial additional incurred costs, such as travel and accommodation, and was greatly helpful to myself and my family. 

I have set up a JustGiving page if anybody would like to sponsor me - if 100 people sponsor me £1.70, I will have hit my target! https://www.justgiving.com/petebigbuzz 

Thanks for reading! 

Pete