At a follow-up meeting during my diagnostic phase in July 2010, the specialist who was investigating my pre-diagnosis secondary care appointment, was clearly suspicious that I had cancer. As the results of my liver biopsy were not yet in, he was not in a position to declare his findings. However, following my revelation about flushing during this meeting, he immediately guessed the biopsy would confirm Neuroendocrine Tumour (NET). I can’t remember much of the conversation but I vividly remember him indicating that of all the cancer issues out there to get, this was one of the better ones. He was using a meter analogy action with his hands swinging towards the ‘good’ reading! I hadn’t gone there that day to receive a cancer diagnosis but he was clearly trying to put me at ease and I’m sure it was with the best of intentions. A little bit of me thinks this scenario is OK but the definition of ‘Good’ before treatment is known and them given, what the treatment outcomes will be, might just set expectations too high! I still think I had an early diagnosis at Stage 4 – even that doesn’t make it good though!
This is a very topical subject on forums and some patients are not happy being told their cancer is a ‘good’ cancer or one of the ‘better’ cancers to get. Whenever this subject comes up it tends to overlap and extend into associated areas including the deception where people look so well so how can they possibly have a ‘bad’ cancer. If I had an opinion, I would say that no cancer is good but it’s true to say that some are worse than others, e.g. certain cancers will kill lots of people quickly and that’s awful – I’m fairly certain that is what the doctor above had in mind.

Some cancers can be declared in remission after a period but some cancers can stay with you for the rest of your life. Some cancers can result in long-term debilitating side effects. Additionally, the consequences of treatment for certain cancers can be difficult to live with, meaning significant lifestyle changes in the long-term or for life. This is precisely why many cancer patients who live with these ‘consequences’ are angry at the suggestion their cancer is a ‘good one to get’.
Dear Doctors – There’s no such thing as a ‘good’ cancer! They’re all bad? By the way – Neuroendocrine Cancer is really SNEAKY!

You may also enjoy these similar and related articles:
I can see my invisible illness – click here
Things not to say to a cancer patient – click here
Shame on you! – click here
I look well but you should see my insides – click here
Things are not always how they seem – click here
Things are not always how they seem Part 2 – click here
Not every illness is visible – click here
Not the stereotypical picture of sick – click here
An Ode to Invisible Illness – click here
Poker Face or Cancer Card – click here
I don’t look sick, sorry not sorry – click here
Dear Doctors – there’s no such thing as a good cancer – click here
You must be doing OK; you’ve not had chemotherapy – click here
Disclaimer
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.
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.
Click here and answer all questions to join my private Facebook group
Check out my WEGO Health Awards
Check out my Glossary of Terms – click here
Please Share this post for Neuroendocrine Cancer awareness and to help another patient
- Ronny Allan’s Newsletter covering August 2026
Summary of August 2026 on RonnyAllan.NET August was similar to the other months of this year but like July, views are down on the previous two months due to 50% of the month spent on holiday. Still a reasonable blog performance – I can’t complain. Other key targets met were three more editions of the Spotlight… Read more: Ronny Allan’s Newsletter covering August 2026 - External Beam Radiation Therapy (EBRT) for Neuroendocrine Neoplasms
Disclaimer: The information in this section is for education only and does not represent a standard care pathway or service. These treatments are not suitable for everyone, and careful patient selection by an experienced multidisciplinary team is essential. Always discuss your individual situation with your own specialist team. External Beam Radiation Therapy (EBRT) is… Read more: External Beam Radiation Therapy (EBRT) for Neuroendocrine Neoplasms - 2026 Surveillance Update from Ronny Allan: “See you in 12 months”
It’s only a couple of weeks since I celebrated my 16th year since diagnosis of metastatic small intestine Neuroendocrine Tumour (NET) at Grade 2 on 26th July 2010. Thinking back to that period of my life, I’m happy but also slightly amazed to be celebrating such a long milestone having been diagnosed with cancer at… Read more: 2026 Surveillance Update from Ronny Allan: “See you in 12 months” - Spotlight: Selenium in Neuroendocrine Tumours (NETs)
Before you read this This information is designed to help you understand how vitamins and minerals work in the body and how certain NET‑related factors might influence them. It is not a substitute for personalised medical advice. Every NET patient is different — tumour type, treatments, surgery, symptoms, and nutritional needs vary widely. If you… Read more: Spotlight: Selenium in Neuroendocrine Tumours (NETs) - Spotlight: Potassium in Neuroendocrine Tumours (NETs)
Before you read this This information is designed to help you understand how vitamins and minerals work in the body and how certain NET-related factors might affect them. It is not a substitute for personalised medical advice. Every NET patient is different — tumour type, treatments, surgery, symptoms, and nutritional needs can vary widely.… Read more: Spotlight: Potassium in Neuroendocrine Tumours (NETs) - Spotlight: Magnesium in Neuroendocrine Tumours (NETs)
Before you read thisThis information is designed to help you understand how vitamins and minerals work in the body and how certain NET-related factors might affect them. It is not a substitute for personalised medical advice. Every NET patient is different — tumour type, treatments, surgery, symptoms, and nutritional needs can vary widely. If you… Read more: Spotlight: Magnesium in Neuroendocrine Tumours (NETs) - Ronny Allan’s Newsletter covering July 2026
Summary of July 2026 on RonnyAllan.NET July was similar to the other months of this year but views down on the previous two months due to 50% of the month spent on holiday. Still a reasonable blog performance. Other key targets met were three more editions of the Spotlight series on vitamins and minerals. See… Read more: Ronny Allan’s Newsletter covering July 2026 - 16 years since diagnosis, I’m still here

I finally made 16 years since I was diagnosed on 26th July 2010. A milestone I was not certain at the time I would reach. However, as things progressed, as treatment was administered, and as I got used to living with Neuroendocrine Cancer, I eventually became more confident this was a possibility with the help […]
- Spotlight on Cushing’s Syndrome in Neuroendocrine Neoplasms
Intro Cushing’s syndrome is one of the most challenging hormonal complications seen in people with neuroendocrine neoplasms (NENs). It can be subtle, severe, or even life‑threatening — and it is often misunderstood. Many patients struggle for months or years before receiving a correct diagnosis, partly because the symptoms overlap with everyday conditions such as weight… Read more: Spotlight on Cushing’s Syndrome in Neuroendocrine Neoplasms - 14th July 2026 – Ronny Allan hits 3 million blog views!
Today, 14th July 2026, I can confirm the 3 million views milestone has been reached. MASSIVE THANKS to you guys for reading and sharing. When I first set up this blog in April 2014, it was just to help spread awareness (….and collect a few pennies) whilst I was walking the 84 miles of… Read more: 14th July 2026 – Ronny Allan hits 3 million blog views! - Spotlight: Zinc in Neuroendocrine Tumours (NETs)
Before you read thisThis information is designed to help you understand how vitamins work in the body and how certain NET-related factors might affect them. It is not a substitute for personalised medical advice. Every NET patient is different — tumour type, treatments, surgery, symptoms, and nutritional needs can vary widely. If you have… Read more: Spotlight: Zinc in Neuroendocrine Tumours (NETs) - Neuroendocrine Tumours – Iron
Disclaimer: This Spotlight provides general educational information about Iron. It is not a substitute for medical advice. Individual needs vary, particularly for those with conditions affecting digestion, absorption, or chronic blood loss. Always consult your medical team before making changes to supplements or nutrition. Before I knew I had metastatic Neuroendocrine Tumours, I was diagnosed… Read more: Neuroendocrine Tumours – Iron - Ronny Allan’s Newsletter covering June 2026
Headline – half yearly point bonus edition Summary of June 2026 on RonnyAllan.NET June was similar to the other months of this year but slightly down on the previous two months due to holiday. Still a strong blog performance. Other key targets met were three more editions of the Spotlight series on primary NET types (colon, thymic… Read more: Ronny Allan’s Newsletter covering June 2026 - Clinical Trials PRRT: From 177Lu to 225Ac: The DOTA-LM3 Antagonist Journey
Disclaimer: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… Read more: Clinical Trials PRRT: From 177Lu to 225Ac: The DOTA-LM3 Antagonist Journey
Discover more from Ronny Allan - Living with Neuroendocrine Cancer
Subscribe to get the latest posts sent to your email.



I totally agree my daughter had her first pheochromocytoma tumor and her right adrenal gland removed four years ago and now she has more
It just invalidates us when they refer to it as a good cancer. I’ll never forget my daughter saying to me, Why couldn’t you just have gotten breast cancer?
Talk about luck, while we were working out my flushing symptoms and found a small carcinoid in my duodenum we also discovered I suffered from MDS that has advanced to Acute Myeloid Leukemia, all within three months from me starting with flushing and itchy rash. The tumour was excised and graded as gr 2 stage 1 with no invasion but my insurance doesn’t see it as being a cancer. I have now started on chemo for the AML in anticipation for a possible bone marrow transplant but my medical aid is delaying the ok for a donor search as my Chromogrannin A is still elevated and they want another Octreotide scan done .Being a surgeon it helped to make the diagnosis early, or maybe I was just lucky to pick up the “good cancer” early just to find out about the other “bad cancer”.
To all of you, everything of the best and Ronny keep up the good work.
Andrew Marx
I remember hearing that if you were gonna get a cancer this would be the best one to get. I think that’s supposed to make us feel better. I would rather hear anyone say whatever it is that we have to live with, the fact is is we are living. Each of us has challenges that are sometimes things that seem insurmountable, and as Ed said, we just Soldier on. It’s all we can do. We are all living with something. And there are days it just sucks. But I am grateful for every day of life that I have Kama as I was told four years ago I had six months. When people tell me that I don’t look like I am no, I just tell them it’s the good-looking cancer. Then they usually don’t know what the heck to say and move on! 😉
Well, I guess “luck” can be good and bad. For me, yes…I am alive but my wife is under constant stress, I am always sick, my cancer has spread all over my body including liver, G.I. Tract, legs, shoulders, ribs, lymph nodes, spine. Pain and nausea/vomiting and fatigue and constant symptoms and my 8 year old son gets to worry about me and maybe lose me to this disease. I used to run in the streets with him, chase him, play games outside. Most of that is gone. It’s horrible. Is it lucky or good to have only one leg cut off in an auto accident and not two? Would you go to that person’s hospital bed and say “Yes, you lost a leg but hey, look on the bright side…you’re alive!” I don’t think so. Would that be the good kind of amputation or auto accident? I think the question is irrelevant and over simplified. Is it luck that I got cancer? Maybe bad luck if you believe in luck. Will I soldier on? Yes, but that doesn’t make it any better.
great point about ‘luck’ Ed. There is definitely good and bad luck! I tried not to distinguish between ‘this cancer’ and ‘that cancer’ or even ‘this illness’. Difficult to find a text to meet everyone’s view! However, I mainly wanted to say that no cancer is good.
Thanks! I knew that. 😀 That is difficult to write about without writing 36 pages. 😀 To many “if then” statements…can you tell I was a programmer. LOL Thanks again!
Don’t forget the ‘else’ 😈
Perfect!! My first doctor said: ” This is the better cancer you could have!! ” But it is not true!!
While I agree that there is no such thing as a good cancer, I am thankful that for me, at least, NETS has been a lot easier to live with than many other cancers would have been.
Yes, ditto. I see so many awful stories in the news about Pancreatic, Oesophagus and certain other deadly cancers that it does make me feel lucky. I could have said more in the blog but I sensed it might have contradicted the message that some cancers aren’t that bad at all (if you get my drift!)