Just another quick update to let you all know what happened yesterday.
So we went to see the consultant at Canterbury Hospital, who had a look at my scans and did a few physical checks to test brain function – stand on tip-toes, with your arms out, twirling your fingers, kind of thing (like you might see police asking suspected drugged drivers to do on ‘Police, Camera, Acton’, should you be into that).
The conclusion seemed to be that yes, my vision is certainly impaired, but beyond that everything else in there seems to be working pretty much as normal – which is good to hear.
They also advised that I reduce my dose of steroids, to just enough to keep the symptoms under control – which will be a bit nerve-wracking at first. On the plus side, it should hopefully reduce the desire to eat everything in sight (increased appetite being a side effect of steroids). Although I must admit to having very much enjoyed eating everything in sight.
The actual radiotherapy itself is pencilled in to begin on the 10th May – which is later than I expected to be honest. However, there are as yet unknown variables in there, such as whether or not I have the third cycle of chemo next week, which will depend on CT scan results. If no chemo, then radiotherapy could be brought forward.
So it’s still a bit up in the air. I will have to get in touch with the Marsden anyway to let them know I can still make my scan appointment next week, so will see what they say about the chemo, and go from there.
A good thing is that Canterbury seem fairly relaxed about overlapping the chemo and radiotherapy. Which I am pleased about – I seem to have been tolerating the chemo pretty well, so am happy to go for both.
That’s about it for yesterday’s news – will write more soon.