G is for Gastroscopy


A couple of years ago I was diagnosed with NAFLD, or Non Alcoholic Fatty Liver Disease, to give its full name. Or, to put it another way,  Cirrhosis of the liver.

Over the last couple of years, I have been prodded and poked as part of the monitoring process. As  yet, I am not on any medication, but I do get regular lectures about my diet and my lack of exercise.

My Hepatology consultant has wanted to carry out biopsies to prove her diagnosis, but I have resisted. I really don’t fancy the idea of someone pushing a needle into my side.So far she has had to make do with me having regular Fibroscans, blood tests and the occasional gastroscopy.

And so it was, last Tuesday, after two years had elapsed, it was decided that it was time for me to undergo another gastroscopy.

I vaguely recalled that the previous procedure wasn’t actually as unpleasant as everyone had told me. So, when I presented myself at reception in the Queen Alexandra Hospital Endoscopy Department, I was fairly relaxed.

On arrival, I was asked to complete a two page questionnaire regarding my medical history. Given the number of times that I have provided this information, over the last  few weeks, I question the need.

After all, my height and weight are still unchanged, I  still wear glasses, and no, I still don’t have any metalwork inside my body. The drugs I take on a daily basis are also unchanged. You would think, in this technological age, that they could print out my record and get me to confirm that nothing had changed. It would save bit of time.

Anyhow, questionnaire duly completed, it was time for me to head round to where the procedure was due to be carried out. I followed the nurse, like a dutiful hound called to heel. But first, we made a detour into a small office space where the nurse talked me through the questionnaire and I pretty much had to answer all the questions….. Again!!! We could have done the form filling and verbal confirmation all at one go. The only difference was that the nurse decided that I needed to provide a blood sample for my blood sugar,

Oh and I had to sign a consent form and in return I was given a standard hospital bracelet.

And then we walked round to the theatre. Where, once again, I was interrogated. Name, rank, serial number.

Then it was down to business. Sit on the table. Lay back. Open your mouth and hold your breath while we spray this stuff, Xylocaine, to the back of your throat. I had been warned that the spray tasted of rotten bananas. Perhaps not quite that bad, but more like overripe bananas. The spray is required to reduce/stop the natural gag reflex when the endoscope is inserted.

As requested, I rolled over on to my left side. And then the doctor was there with endoscope in hand.

He suggested that I might want to close my eyes as he began his hunt for varices.

But I didn’t want to miss the tv show. Unlike two years ago, I had a screen to look at. Full HD, I reckon. So I watched as the camera began its journey down my throat. The doctor was giving a full running commentary as the camera travelled down. It’s a bit like a train journey where the name of the next destination is announced.

Soon we were in my stomach which, much to my surprise, was empty apart from some fluids. In my head I envisaged the doctor, wearing a miners head lamp and wellies, sploshing around in my gastric juices. Strangely, I could feel the endoscope moving moving under my hand, which was laying on my belly, as the doctor had a good look around. So the gastric train reached the terminus and then began the return journey. Like any good tourist, the doctor paused the extraction to take a couple of photos.

And then we were done. Endoscope extracted and the doctor was saying that all was clear. In medispeak “No endoscopic signs of portal hypertension”, no varices.

After a few minutes I was taken to a discharge waiting room while the doctor was writing up his report. A nurse appeared and presented me with an “After gastroscopy care leaflet” Nothing to eat or drink for an hour. This is to allow the effects of the throat anaesthetic to wear off. Too soon and I could choke. After an hour, just small sips of water and if OK gently increase intake back to normal.

I was also given a copy of the doctors report and informed that I would be called in for a repeat performance in three years. And so I was formally discharged and allowed to go home.

Obviously I am very pleased that nothing sinister was seen and perhaps slightly less pleased at the thought of doing this again. But I am glad that they are continuing to monitor for the adverse symptoms of NAFLD.

Bobs Bowel 2


Previous Posts On This Subject

The NHS Poo Sticks game, Colonoscopy, and Bobs Bowel.

I have become obsessed with bowel movements, or rather the lack of them.

After my CTC I restarted taking a laxative, Molaxole, but this was proving to be non productive. As well as the laxative I have also resumed eating normal foods, not the low residue diet, which is remeniscent of baby food.

The lack of bowel movements over the last few days, and the constant feeling that I just ate a full Christmas roast is troubling. The indications are that my tumour is severely restricting the flow in my digestive system.

And that is definitely not good news.

I have been consulting Dr Google, which is not always a good thing. But, in this case the concensus seems to be that, if my tubes are truly blocked, then continuing with the laxative can be counter productive.

Regardless of biopsy results I think it is imperative that the tumour is removed and tout de suite.

As I have been typing this post, and after several fruitless trips to the bathroom, I have finally had success. The fullness that I have been feeling is easing so I think I will carry on with the laxative for the time being. Based on my recent past experience, my bowel seems slow to react. So I have taken another dose of Molaxole and will drink plenty of fluids.

Tomorrow, I will contact the Colorectal Unit for some advice but regardless, I am seeing a consultant on Tuesday with whom there will be a full and frank discussion.

So, I am off now, to make a mug of Bovril.

Stay tuned….

Bobs Bowel


A few days ago, I posted about the NHS Poo Sticks game. There then followed a visit to the hospital for a Colonoscopy which led to my cancer diagnosis.

Apparently my tumour is positioned up at the top right corner in the diagram, where the transverse colon joins the descending colon.

Of course, that is not the end of the saga. We are only just getting started.

Shortly after the colonoscopy, at the meeting with the doctor along with the bad news I was given an appointment date for a meeting with the consultant. That is scheduled for 28th January.

After being discharged I headed home to find that the hospital had already been on the phone. I returned their call and was informed that they had an appoinment for me to attend the hospital again. This time for a CT colonography (CTC). Lucky me. I was scheduled in for Tuesday 21st at 08:30.

That was the good news. The bad news was that I had to go back on the low residue diet. OK, it was only for two days this time, starting on Sunday. On the Monday before the CTC, I was to start taking a liquid laxative. Two doses, one at 08:00 and the other at 18:00. No food after that time, just clear fluids until after the CTC.

The liquid laxative, Gastrografin, also contains a dye (contrast medium) that contains iodine and it helps to clearly show the colon on the scan.

Once again my imagination ran riot but reality was a lot simpler. I was expecting to spend the day on the loo, but after a brief eruption in the morning, I suffered nothing until the following morning. Even after the second dose.

Tuesday morning arrived soon enough and I took myself of to the hospital. No sooner had I arrived in the reception area than I was called through. Given a hospital gown to change into and told to take a seat in a waiting area.

I was then called through to have a cannula fitted. This was needed for the dye that they would inject during the scan. After a brief wait I was shown into the scanner room. I have had CT scans before so my anxiety levels were really low. And so it was up onto the scanning table where the unpleasantness started.

Firstly I was asked to lay on my side with my knees up towards my chin. Once in position a tube was inserted into my back passage. This was for the gas that they were going to use to inflate my colon.

As the gas flowed, so my discomfort increased. Initially there was the sensation of my abdomen bloating. This was soon accompanied by stomach cramps which grew in intensity. I was asked to lay on my back and I was threaded through the eye of the donut.

The discomfort was increasing.

They then injected the dye and we played thread the donut again. After a couple of passes I was asked to turn on my side.

Still the discomfort was building. So much so that I was muttering to myself. Something along the lines of “enough already”, “get me off this thing”, “please make it stop”. You get the picture.

After a couple more passes through the donut they came in to put me out of my misery. The gas pipe was extracted and I was led out of the scanning room, across the corridor and shown to a toilet.

It was there that the process of decompression began. It was also there that I got changed into my street clothes. I then went and sat in a waiting area but it wasn’t long before I headed back to the decompression chamber, and then back to the waiting area.

After a short wait I was invited into a small room where my cannula was removed, and then I was discharged.

Over the last few years I have undergone numerous procedures. But this was by far the worst. I have had CT scans before but the added gas takes them to a whole new level. Definitely an experience that I am not keen to repeat.

I am not Jumping Jack Flash and it definitely was not a Gas, Gas, Gas.

Now, I am eating a relatively normal diet but to ensure that my bowel doesn’t become completely blocked I have been prescribed a different laxative, Molaxole. This I have to drink twice a day. It doesn’t taste nasty but it isn’t pleasant. I have to add some orange squash to make it more palatable.

Yuukkk!

So, now I have to wait until Tuesday and the appointment with the consultant.

I’ll be in touch…..