Tuesday, 28 October 2014

The Paradox of the End


It’s the 28th October 2014 – last day of radiotherapy, last day of treatment. I’m sitting in the little flat in Brighton overlooking the ocean wondering how to write this blog post. It’s not an easy one. For the last few days I’ve been getting phone calls, texts, emails… of joy, excitement, congratulations that I’m ‘at the end’. Somehow I don’t share these feelings though, even though I appreciate the love and support, as ever, and even though I’m relieved in many respects to be at the end of treatment…

I had my final appointment with my oncologist yesterday. When I say final appointment I mean the final one that I’ll have during treatment. I’ll continue to see him for ‘check-ins’ when appropriate. I say check-ins as opposed to check-ups because I found out yesterday that as far as he’s concerned I’m cured. He said he can’t absolutely guarantee that but he has now put me in the cured box unless anything in the future indicates otherwise. Obviously this is good news. The hard part is that there’s nothing that they can do to ‘check-up’ on me over the coming months or years. Having had the bi-lateral mastectomy there’s no chance of tumours recurring the breasts – obviously… they’re gone. Then, checking the rest of the body for any spread through full body scans is not what they routinely do, unless something abnormal was to show its face. This, I found a difficult concept to get my head around and it triggered off every difficult feeling I have about coming to the end of treatment. I’ve read about how ‘the end’ is often an anti-climax and can be very hard for patients but hadn’t, before now, had the experience of it.

Those few that have been around me have seen how hard treatment has been, especially surgery and chemotherapy. And those of you that have been keeping in touch via my blog or other means have probably also seen or felt the intensity of the process. This I cannot deny. There’s something rather weird that surfaced yesterday though about the safety in treatment. However tough it is (and don’t let me undermine that) I didn’t realise there is also comfort in it. There’s no chance really (as far as I understand) that cancer can grow during it (chemotherapy). So now I find myself being ‘let off the leash’ and into the unknown – no treatment, no proper check-ups, just me.

There’s an interesting paradox in it all, which I wouldn’t have guessed before recent days. Someone said a couple of days ago how nice it will be for me not going in to hospital for an appointment every five minutes. Of course that’s true. Without a doubt I wouldn’t wish to continue with all of that. Hospitals, journeys to and from the hospitals, appointments and treatments are grim. But… in many respects you’re in someone else’s hands. I’m now in my own hands again and that responsibility seems hard.

I guess the hard part is the mind. It seems obsessed with the negative. I’ve been told that I’m now in the ‘cured box’ as far as my oncologist in concerned but the fact that that can’t be guaranteed, or checked, is what mind wraps itself around and gives me grief about. It’s not even vaguely compelled by the fact that I’m likely to be cured – what a blessing.

So… the onward journey is about learning the stay afloat in the ocean of fear that the mind presents. They say in the yogic teachings that by looking at the fear face-on, not pretending that it’s not there, is what gets you through it. A bit like when you put a fist of pressure on a knot in your back – it has no choice but to release eventually. Being scared of the return of the cancer is something that I must now live with, but the gift in that is that I get the opportunity  to learn to overcome it. Imagine life, when fear doesn’t get in the way! There’d be no stopping me. And that’s what I strive for. It is my hope, my sincere hope, that I learn to understand the patterns of fear, and see it each time it arises, before I sink into it. It’s a game I will play with my own mind and it is that which will determine the quality of my life from now on in.

---

I guess on that note I draw (at least, this part of) my blog to a close. Maybe I’ll continue to use this space as a means to communicate my onward journey. Maybe I won’t. But ultimately, here’s hoping…praying… that this space, if and when used, is used through growing health. I want to thank you all for the support and love that you’ve given me so far on this journey. I’m ridiculously blessed to have you all by my side. Love love xxx 

Saturday, 11 October 2014

Radiotherapy Begins


3 radiotherapy sessions down, 12 to go…
So far it’s all ok…

I’m not going to write much now because my arm is playing up a bit but just wanted to fill you in briefly.

It was so completely amazing starting to feel well again before radiotherapy started. I had four weeks in between my last chemo and the start of radiotherapy, so the fourth week was really quite a treat. Every time I had a conversation with someone where I could put a bit of energy into what I was saying or when I walked somewhere with a bit of pace or for a sustained amount of time, it felt incredible beyond belief. I never want to take that for granted again – how amazing energy is, how amazing it is to have the life force within us to talk, to walk, to think…

We moved down to Brighton on Tuesday to a gorgeous flat we’re being leant on the sea front. Radiotherapy then began on Wednesday. Funnily enough, when we moved to Brighton it felt like we were going on holiday. Even though it’s for  radiotherapy the change of scenery is still a treat.

I’m not feeling massively motivated to go out and about. I’m still feeling quite internalised. But I did venture out last night (for the first time in as long as I can remember) for dinner and to the opening night of the Brighton Comedy Festival. I’m not an easy one to get laughing out loud with stand up but there was quite a lot of good ol’ belly laughing that went on last night, so that felt good… so I’ve had a good intake of laughter medicine and it was exciting being out and about.

I’m back at the cottage for the weekend now and then back to Brighton on Monday to continue with treatment. I’ll keep you posted on how it goes…xxx