Jelly in the mould

It’s been a full couple of days.

Yesterday I had 3 hospital appointments, or 2 appointments and 1 treatment session to be precise.

I turned up at Counter 5 for my first appointment, in the morning.  My stomach was churning as I knew this one involved a blood test.  Blood tests involve needles.  Needles hurt supersensitive chemo skin.

Sure enough, I was directed towards the Lab and the row of seats at the blood letting counter.  When it was my turn, I gestured towards my still bruised right arm and asked as usual if they would be gentle with me.  I have to say, that the Lab staff are exceptionally good at these needle sticks.  Even if I said nothing, I am sure that they would still be very gentle.  The needle lady looked at my poor arm and its battered veins and set up a special blood drawing thing.  She even gave my arm a quick spray of numbing agent before she started her task.

After a wait for results, and a welcome cuppa, it was my turn to see Dr P for my overall check.  The blood had done well and showed that my body is slowly recovering from the onslaught of chemo.  Also importantly, it is recovering from the effects of the steroids which had pushed glucose levels up throughout the chemo.  Kidney and liver functions and cholesterol were also in pretty good shape considering everything,  Dr P was very happy with my general progress and noted my positive outlook and lifestyle changes I had made which she said were reflected in the test results.

So I came out of my appointment really smiling for once!

After a couple of hours, I was back at the hospital and waiting for my transfer to the Cancer Hospital for radiation and an appointment with Dr C, the radiation consultant.

The treatment went smoothly and quickly as usual.  Zap another one finished. and I headed upstairs for the final appointment of the day.

I did not have to wait long before I was called to see Dr C.  He seemed happy with the progress of the radiation and had a look at the blood test results I had brought with me.  He said there was no need for further blood tests – my encouragement and mention of the bruised arm perhaps influenced him 😉 .

He also explained to me that there would be a slight change to the procedure starting from today.  A gel would be applied to the area having radiation from now on.  It did not dawn on me to ask why or anything else about it.  I seem to have this “yeah, whatever” approach to what has to be done.  I have thousands of questions about the treatments, effects, prognosis and procedures, but never seem to have a why question.  Just do what needs to be done.

So when I turned up today for my treatment, the staff told me I would be having this Gel thing applied to the radiation area.  I asked what this was for.  Apparently, it draws the radiation skin-wards so that the surface of the skin area is targeted in the last 10 sessions.  This is when the skin really starts to colour and darken.  My skin is already pretty dry and irritated so I am not looking forward to the sunburn which is surely coming my way.

As I am always flat on my back, pressed into my mould and completely immobile I had no idea what this Gel stuff was like or how it was being applied.  I tried to catch a glimpse of it in the reflection of the big machine above me but could not really see anything.  There were a couple of test beeps to check the angle and before long I was back in the daily routine.  Beep, beep, whirr, click………..

Once the zapping was over, the staff came back to prise me from my mould and release me for the day.  Before I sat up, they asked me if I wanted to see the Gel as they removed it.  It was not quite what I expected.  It was a bit like a computer mouse mat (but larger) and made of a clear kind of gel, in a semi solid state.  It was peeled off the radiation area and taken away, probably for cleaning and preparing for the next jelly session.

Now that today’s session is complete, I have moved into single digits with 9 sessions left.  They will all be jelly sessions and I hope that my skin stands up to the concentrated rays.

It’s clear that the cooking course is moving forward nicely, and I am clearly moving towards the dessert stage.  So, when the final jelly comes out of the mould, I think I might treat myself to an ice cream to go with it!

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One thought on “Jelly in the mould

  1. Just had session 7 – which means I am now more than a third through – sounds good but in reality means another 13 sessions! My last five are going to target the skin so wondering whether I will be having jelly and ice cream too! From what other people having been telling me I think I will be putting the ice cream on my poor reddened boob to cool it down!!

    Glad the trip to the hospital went OK – it is good to come out with a smiling face 🙂

    P x

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