
Neuroendocrine Cancer: I hadn’t heard of it until I was diagnosed with it
My diagnosis came with many strange words including, “carcinoid” and “neuroendocrine” ……… can you spell that please, I said to the doctor. I had a
Every year I cast my mind back to this time in 2010. Diagnosed on 26th July that year, I was in hospital from 8th – 26th November, an extended period due to complications. At that point, I had been keeping my diagnosis within close family and friends and my manager at work. People at work and my wider list of friends were probably wondering what was going on with me.
Cleary, I let my emotions slip by posting this on my personal Facebook profile on 20th November 2010. Perhaps this was my way of opening up. To be honest, the first few days I was suffering a lot of fatigue and brain fog from the morphine/painkillers. The thought of posting stuff on Facebook was far from my thoughts. I was receiving newspapers from day 3 but could not even focus for more than a couple of minutes. Then on 20th November 2010, I got hold of my tablet and typed “Feeling perkier”. It was a milestone.

That was 11 days after the surgery, so I guess it took a while to feel almost normal. I had a big surgery! I had some issues along the way. But after 10 days I had got through these issues with the help of the doctors and nurses and felt stronger, the light at the end of this particular tunnel was shining brighter than ever before.
By the time I wrote about that experience on 17th November 2015, some of the detail had gone. I also tried to write about it with some amusing recollections. I do laugh about some of it, particularly:
1. the suppository story,
2. the moving picture when I was on the PCA (pain control),
3. the refusal to do physiotherapy one day,
4. the urine bag leak on the CT scan.
In hindsight, I wish I had kept a diary of some sort covering the whole period. There are no pictures of machines or me with tubes etc, that is not my style.
To say there wasn’t a time during those 18 days when I was scared would not be truthful. I once got a message from someone who said, after reading my surgery experience article, that it scared her. I’m so sorry that person was scared, I don’t want to scare anyone, I wanted to tell my story the way it happened but at the same time provide hope given that it was such a long time ago and I feel fine.
I am not a doctor or any form of medical professional, practitioner or counsellor. None of the information on my website, or linked to my website(s), or conveyed by me on any social media or presentation, should be interpreted as medical advice given or advised by me.
Neither should any post or comment made by a follower or member of my private group be assumed to be medical advice, even if that person is a healthcare professional. Some content may be generated by AI which can sometimes be misinterpreted. Please check any references attached.
Please also note that mention of a clinical service, trial/study or therapy does not constitute an endorsement of that service, trial/study or therapy by Ronny Allan, the information is provided for education and awareness purposes and/or related to Ronny Allan’s own patient experience. This element of the disclaimer includes any complementary medicine, non-prescription over the counter drugs and supplements such as vitamins and minerals.
Thanks for reading.
Blog Facebook. Like this page please.
Personal Facebook. Like this page please.
Awareness Facebook Like this page please.
Follow me on X (formerly twitter)
Check out my online presentations
Check out my WEGO Health Awards


My diagnosis came with many strange words including, “carcinoid” and “neuroendocrine” ……… can you spell that please, I said to the doctor. I had a

Ronny Allan’s ‘PoNETry’ © series can be shared with poetry credit to: RonnyAllan.NET Thanks for reading Ronny I also have one about Lanreotide (or “butt

When I was diagnosed, I didn’t even feel ill. It was therefore a bit of a shock being told I had metastatic cancer, advanced enough to

I was assessing performance of the awareness period in November 2025 on Facebook and was astonished to find the size of my reach on that

Here is the monthly summary of November 2025 on RonnyAllan.NET – Every share helps someone understand or even work towards a diagnosis, discovery of the

Discover more from Ronny Allan – Living with Neuroendocrine Cancer Subscribe to get the latest posts sent to your email. Type your email… Subscribe

Bone metastases in Neuroendocrine Tumours (NET) Many of you will know that I am a stage IV small intestine NET and I have one bone

What is Radioligand Therapy? When you browse the internet, you may see the term “Radioligand Therapy (RLT)” and wondered what it was. There’s a simple

D Day I was 54 years and 9 months old at diagnosis on 26th July 2010. For the first few months, I had no idea
Subscribe to get the latest posts sent to your email.
Subscribe now to keep reading and get access to the full archive.