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Our Story

Cancer Treatment

In November 2016, we started this blog after John was diagnosed with advanced Metastatic Prostate Cancer. It was initially meant to keep our friends and family up to date with John's latest health news. However with his continued good health, it has now turned into more of a travel blog since he took early retirement in 2017. We will continue to update it regularly with our latest travels and any other news. We hope you find it an interesting read. Thank you for all of your support and good wishes.

Two updates in one day

February 2017 Posted on 15/02/2017 12:02

Since the last chemo treatment John has been into work most days, and only stayed away when colleagues were suffering from colds, and one day when he felt pretty wiped out (the pattern shows that his energy levels dip 10 days after a chemo session). He has actually taken this week as annual leave, expecting to feel well in the week of the next chemo session. More blood tests were taken last week to monitor the effects of the Metformin clinical trial drugs. These results were good (neutrophil levels were 1.3 compared to .5 at the same stage 3 weeks ago, and PSA had reduced to 2.2), so he has been given a longer 3 month prescription. On Monday we had an appointment with Dr Rimmer who appeared happy with how John is tolerating the chemo and gave the go-ahead to ‘come in to be poisoned again’. More blood tests yesterday in readiness for the third chemo session tomorrow.
John’s initial investigations started in September last year, just as Steve Hewlett began his Monday afternoon Radio 4 PM interviews about his cancer diagnosis, treatment and participation in a clinical trial. At the time we had no idea how compulsive his honest, personal account of his treatment would become. It feels as if we have learned the cancer language with him. If you haven’t been following his account it really is worth a catch-up on iPlayer.
You may be aware that we are rather obsessed with wood, and much of our spare time is taken up with collecting, cutting, splitting, stacking and burning wood on the log boiler which heats the house and hot water. The wood is a free resource, but we also get paid an allowance from our lovely government for burning it (The Renewable Heat Incentive payment). This has really helped to achieve our aim of having a carbon-neutral house. Dealing with the log boiler is quite a time-consuming physical activity, so we have decided to install an air source heat pump (ASHP) which can take over when we don’t have the time or energy to use the log boiler. The ASHP is being fitted this week, and although it should be capable of heating the house just by extracting warmth from the air, it will require electricity so it won’t be as environmentally friendly as the log boiler. I suspect we will only use it when absolutely necessary.
Well, no blogs from us in over a week, and you get two in a day. John managed to post his just before me!



Here we go again!

February 2017 Posted on 15/02/2017 11:45

Well, I really don’t have much to say this time! This last chemotherapy cycle has been pretty uneventful. Having had two full sessions there is now a pattern to how I feel. During the first week I have a drugged feeling, a bit hungover and tired. The second week is when my immune system and red blood cells are knocked about a bit. This leaves me feeling tired most of the week. The third week is recovery time. This gives me time to build myself up ready to be poisoned again. ‘Poison’ is the word that the consultant used to describe the docetaxel chemotherapy drug that I am having. It was slightly alarming to hear that, but actually it is a good description of what your body goes through. The dosage is worked out carefully according to your height and weight, as it would not be good to receive too much.

Having now had several visits to the MacMillan cancer centre at the West Suffolk Hospital, we have been very impressed with the communication within the department. Whenever we have had appointments it is very apparent that all the staff have clearly discussed my case in advance. The appropriate drugs are all ready for me. Even when I have had go to the pharmacy to pick up the metformin for the clinical trial, the receptionist seems to be expecting me and finds my medication immediately even though there is a room full of people waiting. It makes me feel like I am having private medical care in an NHS hospital!

One good thing from this last cycle is that I did not lose any more hair. Having lost a good amount last time, I thought it would all be gone by now. So, for the time being I still have some, although it is all grey. It will be interesting to see how it regrows. Our JustGiving page was very successful when Dan decided to shave his head in support of my hair loss. Ellie has now declared that she is going to do the same in a couple of weeks time. She is going to donate her hair to the Little Princess Trust, which makes wigs for children suffering from cancer. We will post some before and after photos later.

Anyway, I am all ready for tomorrow. Six weeks down, twelve to go.