A tumultuous month

October has been a month in which my life has once again been turned upside down. I’ve not posted here on My Trike since I installed the Savannah’s new screen but below are what I posted on Facebook since that time.

October 7

It seems that Mr C has called on me again. Dr T says that I fought one battle and won and that if I have to fight another I will win that too.

Even so the thought of having to do so again is terribly demoralising and it is very dispiriting to know that the control over one’s life has to be handed over to others no matter how caring and professional they are.

At such times what value can possibly be placed on the love and support of friends and family.

Afterwards I was summoned to the hospital in Perigueux for several days for tests.

October 11

I’m back. They gave me a weekend pass from 5.00 pm on Friday. It gave me a chance to cut my grass and sort out a few things at home but I had to be back by 5.00 pm this evening. Now I’m waiting for tomorrow when I’ll get the news about last week’s results. The young intern with whom I was speaking before I left was already hinting at what they might be and I’m not raising my hopes too high. I’d be lying if I said I’m not worried. Wish me luck.

October 15

I’m back for a quick update. Sometimes in life we don’t get what we want and think we deserve but just have to accept what we’re given. For me this seems to be one of those times.

It looks like I’m on the receiving end of a double whammy because as well as now being diagnosed with colon cancer it appears that the lymphoma for which I received treatment in 2017/18 and have been in remission for since then has also returned.

I have no idea how bad the situation is and neither at this point does the amazing medical team in Perigueux in whose hands my life now rests. I’m back home for now after having had three scans in three days, the last a TEP scan ( or PET scan for Brits) at 10.00am yesterday. The medical team is now analysing and discussing all the results before deciding what the way forward will be and calling me back in again.

That’s all for now. I’m not going to keep posting about my situation and projecting my problems onto others. I will see you on the other side. Best wishes to all.

I then underwent a physical and psychological evaluation and had a consultation with the surgeon who operated on me the last time I was diagnosed. Subsequently I posted the following yesterday.

October 28

They never said it would be easy, but…

Within days, literally, I had three scans, a detailed physical and psychological evaluation, a consultation with the same surgeon who previously operated on me when I was last diagnosed and then received a treatment plan. They can’t and won’t make any promises and the surgeon especially put on a very optimistic face, but the surgical and oncological teams here think that my illness is eminently treatable.

After going through a very black period anything remotely positive was very good news to me and this was more than I could have hoped for, but although there is now a small light at the end of the tunnel, it’s still a long way away.

I was told that although my cancer is operable, after which I will have to have a temporary stoma bag, when that has been removed after a couple of months I would be left with more or less my original bowel function. This was very good news as I’d said that I’d rather be granted 5 more years without one than 10 more years with and they assured me that this would not be necessary. This was a great comfort.

However, this won’t come without a price because before an operation will be possible I’ll have to undergo an intensive program of radiation and chemotherapy every day for 5 weeks. Previously I’d had a tube inserted into my chest, which I subsequently asked to be removed, delivering the chemo directly into my heart but when I asked about this I was told that this time the chemo would be administered by mouth. However, I’d probably find the radiation a bit gruelling and we’ll have to see how that goes. But I have cause for much hope.

I finally asked the surgeon what I should do while they are making the plans and preparation for my treatment. He said to keep doing what I usually do and make no changes to my life, and while I feel up to it that’s what I’ll be doing. So yesterday as it was fine I went out into my garden and resumed work on the base for my proposed workshop.

My terrace will eventually be coming up one way or the other so I decided to uplift some stones from it to make a ramp to allow my excavator to get down into the hole I’m digging for the base. The reason is that the height of the earth at the back of the hole has to be reduced to make it level all around and as my excavator’s boom can’t reach the back of the hole from the front, the best way to do it is to get the excavator down inside it.

It was hard work the more so as I haven’t been doing anything very strenuous for some time but while I can that’s all going to change. I’m not ready to give up yet.

By the way, I’m not posting this kind of stuff to engender pity or sympathy from my readers. What I’m hoping is that from the keywords contained in my posts others who are diagnosed with similar problems will find their way here and read them and that they will also come to the same conclusions that I have. You must never give up and must keep looking for and moving towards that light at the end of the tunnel however far away it seems to be.

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So while I can I shall be trying to make my life go on as usual. I rested yesterday but I am writing this in the early morning and today I intend to continue the work I restarted yesterday and look forward to making more progress. I’ll post how things went later.