
Before & After The Operation
Sorry about the photo. No matter what I do I just can’t get a smile out of myself when I take a bloody selfie. I’m just impossibly useless when it comes to this. So apologies folks. I know it’s grim.
7 A.M, Friday 15 January, 2021
So in a couple of hours I will be under, out of it, lacking in consciousness, under anaesthetic and completely unaware about what a nameless surgeon of unknown skills will be doing to my throat or about the cameras that will be inserted down my throat to show the inside of my body and organs.
Oh well, as my Mum used to say “What you don’t know can’t hurt you!”. Sorry Mum, not very wise words.
So as the kookaburras sing their serenade out in my backyard it is time to pack up my computer and get Georgie out of bed to once again make the trek south east to the old homeland of East Bentleigh.
Before & After the Operation
We arrived at the hospital at about 8.20 a.m, 20 minutes late but no-one was pissed off or phased. As usual I wasn’t really, really nervous but I was nervous enough to gently “wring” my hands, Georgie noticed so I can’t deny it.
The staff were fantastic as usual and answered any questions that I could conjure up, to the best of their ability.
Georgie stayed will me until they wheeled me away which wasn’t so bad because I ended up being second in the morning’s operation queue.
I whipped off my clothes and slipped into my little standard issue hospital outfit and then watched Georgie leafing through her Instagram posts while I lay on the gurney like a Roman senator about to indulge in a feast.
I did have a chat with a couple of the surgeons while I waited. This was a double edged sword. They were great but re-affirmed my deep fears that they only see their therapies as being valid.
By the way I discovered the unmade surgeon had a name. It is Charlie to the nurses and Charles to the patients.
Then it was time to say goodbye to Georgie.
I made the obligatory parade through the hospital on the gurney toward the operating rooms at about 10 a.m and arrived, I felt like waving to the people in waiting rooms and passing hospital staff.
I was in the actual operating room close to 10.30 a.m after being put in holding mode for about 20 minutes. By now I felt like one of the gang and quite comfortable but still anticipating the moment between wakefulness and unconsciousness after the anaesthetic gets pumped in. Everyone was chatty and I tried to make a few wise cracks to “:prove” that I wasn’t a wimp.
That transition between being aware and not being aware happens so fast that you don’t quite notice it and then you’re out until you wake in recovery area after the operation.
For some reason I just never seem to be able to remember the names of the procedures so I’ll use layman terms. Cameras down the throat to do further visual investigations and scraping more mucous tissue from the deep back of the left side of my tongue, what they go for is hopefully to scrape off enough material to find “the primary” via pathology.
Then it was OVER. No time seemed too have passed but I could feel that my throat was a bit tender.
I spoke to Megan who was there during the operation later in the afternoon and it looks like they didn’t find anything abnormal during the operation so it’s now up to pathology to find whatever they can. I’ll be seeing the Head and Neck team at Monash next Thursday afternoon to get their diagnosis and recommendations.
My next big hurdle will be to peacefully and diplomatically co-ordinate the findings from the RGCC CTC test and any postulated outcomes from my natural therapies with the mainstream oncologists who, based on their training and experience, believe that the only viable options are radiotherapy, chemotherapy and surgery.
So back to “now”.
I’m in a ward that could be named “Oldmansville” 4 grey haired or bald old blokes in their 60-70s all with some sort of cancer.
When I returned from Recovery I really didn’t feel much like talking. I was still “purring” on my own version of Cloud 9.
After about an hour I decided to make an effort and engaged in a relatively decent conversation with 62 year old Greg in the bed to my left. He has a pretty intense lung cancer and is also pursuing some sort of natural, alternative therapy.
I overheard a conversation that he was having with a doctor and when he brought this up he was politely and instantly slapped down when he inferred that the natural treatment may have contributed to the slight diminishment in his tumour. The doctor was adamant that the recent dose of chemo was 100% responsible. No proof, no evidence, no interest in what Peter might be doing as an adjunct, just simply “I know what I’m talking about!”. Now this might be true but at the same time based on the lack of scientific explanation it could be also just raw pride on the doctor’s behalf.
I’m afraid that that’s what I’m going to be up against.
So overall today hasn’t been a complete tragedy. I’m even sort of enjoying myself.
It’s 5.20 p.m now and Georgie is on her way to see me for a while. That happened and now it’s 7.45 p.m and Georgie has just left the building, just like Elvis. I had the foresight to buy a really nice piece of Barrumundi yesterday from Cannings in South Yarra. I baked it last night and ate it for dinner tonight with a simple Greek Salad that Georgie brought in for me. I had a bit of Coconut Yoghurt earlier and some MCT oil so this should get me through the night in one piece. I always take my own meals on airplanes and hospitals, works for me.
The only and possibly the biggest deprivation all day has been missing my black coffee this morning because I had to fast before the operation.
I got a bit more chit chat going in the ward earlier. I keep making jokes about cancer, nothing too insensitive, because I want to do what I can to destigmatize the word. This word has so many meaning, so many outcomes, so many remedies that it needs to be re-constructed and re-defined and disemboweled.
It’s hard work getting a flowing conversation going and I’ve done my duty. I got the party going and now so it’s time for computers, iPads, youtube podcasts, good music through earphones.
More tomorrow morning when I am armed with a dark, steaming, aromatic black coffee.

Overall I'm getting better and better with firing up the conversation in the ward. It's a bit like throwing petrol on a fire that's almost out. It flares up in a flash of glory and when I stop talking the fire goes out almost immediately. But it's fun while it lasts.
Saturday Morning
Still in hospital at 9.23 am. Overnight was not quite as relaxing as it could have been due to Thomas, the nurse. I called him “Tank Engine”, not out of any animosity but it’s just what I do to remember people’s names.
Thomas’s unfortunate job was to wake me every 4 hours to do my biometrics, you know, blood pressure, pulse, stuff like that. So I would drop off into a pleasant state and be in the middle of a lovely dream and then feel a light touch on my left arm and a gentle ”Gary” and robotically present my arm. At the 4 am session he noticed blood and went into a slight panic but it was simply that my canalu had come out of my left hand and blood had dribbled onto the floor and sheets. After the wet cloths and then the dry ones I was wide awake.
I did get through the night quite well overall and got into the shower at around 8.30 am, hot then cold. Got dressed and returned to the “Men’s Club” morning council pow wow.
I’ve been alternating with chatting and writing most of the morning. At one point I got all excited about going to the cafe and buying a lovely black coffee only to be thwarted by the hard cold info that the coffee shop was closed on Saturdays, so I had to settle for a bland tea bag in hot water.
I have to admit that my throat is hurting a bit more this morning than it was yesterday so I succumbed to my second lot of Panadol about 30 minutes ago.
I am now waiting for the registrar to come through the door to give me my release papers. Hopefully sooner than later.
Sunday January 17
I’ve been home for almost 24 hours now but it seems like just a few hours.
The most striking thing is that while I was still in the hospital I felt pretty good and like last month I thought that I would get home and get on with life as if everything was normal.
As soon as I got in the car I realized that it wasn’t going to be like this. How could it be after a general anaesthetic, paralytic drugs and painkillers pumped into me during the operation!
When I got home I made some food for myself. Hunger was what I was most aware of. Georgie stated talking about toasted cheese sandwiches in the car so my thoughts drifted from the salmon that was waiting for me in the refrigerator to going to Aldi to buy a loaf of low carb bread (5 carbs per 2 slices). When O got there I was guided by my hunger and bought haloumi, coconut yoghurt, blueberries, bocconcini and a few veggies.
So I got my toasted cheese sandwich, which BTW was delicious. I had it with a salad.
Then I filled the bath with hot water and epsom salts and stayed in it until 5 p.m and got out with shrivelled skin but I had also absorbed a huge amount of magnesium which I really needed.
Still groggy, I decided to play the guitar so I went down to my music room and started playing, not so well mind you. Then I stood up clumsily and knocked my new Spark amp of the desk and it crashed to the floor. Looks like it’s not working anymore!
The most and only positive thing about this was my reaction. I didn’t go into my normal anxiousness and self loathing that I generally do in moments like this. I was actually quite calm and accepting. That in itself was enough to counteract the loss of the amp.
My throat is more painful than I was expecting but hasn’t yet quite reached the level of pain that I experienced after the first operation. I’m hoping that it will remain that way but based on the last recuperation the pain got worse every day for a week and then subsided for a week so I’m yet to see. The doctors did tell me that it may be worse this time.
Later in the evening I watched a new French series win Netflix called “Lupin” with Georgie. Well we watched 2 episodes.
Finn went across to Yarraville to spend the night with Josh and Luca.
Slept OK. Lucid dreams. Woke a couple of times for brief moments but overall I had a relatively good night sleep.
And here I am again this morning typing on my Mac with the same 2 fingers that I always do. For the amount of writing that I do you would think that I’d invest the time in learning how to touch type but I think that I need the “slowness” of 2 finger typing to think my words and thoughts through.
One thing I did watch yesterday was a Rick Beato podcast on the albums that came out in 1991. Pearl Jam, Nirvana, Soundgarden, Guns and Roses etc. What an amazing g period this was for Rock music. Shit, when you turn the radio on now all you hear is bland auto tuned bullshit. Things were still raw and exciting back then. It seems like yesterday.
My next challenge is coming up next week. Integrative medicine versus mainstream medicine. I really don’t think the pathology will find the primary. But on a more positive note the CTC (circulating tumour cells) test results will be back in around 2 weeks. I’ll also be seeing Dr Eng before I see the mainstream oncologists next Thursday.
My dilemma now is how to diplomatically tell the Monash oncologists that I want to wait for the CTC results and some IVC treatments before I start the radiation that they a certain to recommend.
This is a bit like “once the jug is broken it’s not going to be easy to put it back together although I will still be able to pour water out of what will then be an imperfect jug”. This is the scenario that I don’t want. The cure being almost as bad as the disease.
I’m sure I can work this out.
My next big plan is to write something that outlines all of the different actions I am taking since finding out that I have cancer. I’ve made an initial list and it’s huge. I’m hoping that I can put something together that will be instructive, easy to read and useful for men in my age range who get diagnosed with cancer and even how not to get it in the first place.
So for the next couple of days I’ll need to relax. Tomorrow I’m back to the hyperbaric oxygen tank and hopefully I’ll get onto the IV.



Comments
Like alway Gary, it’s a pleasure to share your thoughts, thanks for being so honest and generous. Stick to what you believe.