Neuroendocrine Cancer – shh! Can you hear it? (…..I didn’t)


sshh - can you hear it?
shh! – can you hear it? I didn’t.

The sooner any cancer can be correctly diagnosed, the better chances of a curative scenario for the person concerned.  However, some cancers are in the ‘difficult to diagnose’ category.  Neuroendocrine Tumours (NETs) are in this category due to the vague symptoms which may be mistaken for other diseases and routine illnesses. This is one of the reasons there have been many lengthy diagnostic delays.  In many cases, it can be very quiet leading to incidental diagnosis at an advanced stage.

In some cases it can be a little bit noisy. For example, some of the most common misdiagnoses appears to be Irritable Bowel Syndrome (IBS), asthma, or menopause.  Patients complain of abdominal pain, wheezing, shortness of breath, diarrhea, flushing, palpitations and a whole host of other minor issues.  There are even extreme cases where patients have been told they may have a mental illness following constant visits to their local doctors. These cases can lead to months or even years of delay from the onset of symptoms, with around half of patients diagnosed at an advanced stage of disease and metastases at initial presentation.

I’m not totally up to speed on what happens overseas, but in the UK, you normally only have 10 minutes (5 in some scenarios) to see a doctor (although my own experience is that many ignore that rule and if they sense a big issue). No matter how hard we push, this can sometimes be insufficient to diagnose or even suspect NET cancer (or indeed many other diseases).

A NET Cancer diagnosis is more likely to be as a result of a number of visits where a picture can emerge and even then, a referral to a ‘symptom’ specialist may not necessary lead to an immediate discovery of a NET cancer. In fact, a ‘nothing serious found’ referral back from secondary care/specialist to a person’s GP/PCP is not uncommon.

There is no harm in targeting GP/PCP but they are more likely to be following instincts by referring due to symptoms rather than in the game of diagnosing obscure cancers which look like other things. I’m a big believer in primary care being the trigger for ‘something‘ which will hopefully be figured out at secondary care where you are more likely to get access to scans etc. In fact there is data to suggest that ‘symptom specialist’ frequently refer patients back to primary care, indicating the education at secondary care level may be a better focus for NET cancer awareness.  NET Cancer is dangerous despite it’s normally indolent course.  It has a propensity to metastasize meaning that the chance of a curative scenario is vastly decreased for many. It can kill if left untreated.

There is new data confirming the incidence of NET Cancer is on the increase and it’s no longer rare – I’m certain this is due to increased awareness, more efficient diagnostic tools (including Ga68 PET Scans) and better reporting methods, e.g. Lung and Pancreatic NETs now being properly reported as NETs rather than Lung and Pancreatic Cancer respectively, particularly at Grade 3.  This is great news.

However, it’s still a ‘quiet cancer’ and there are probably hundreds of thousands out there still to be diagnosed.  There’s a whole invisible patient population out there somewhere. 

Neuroendocrine Cancer – shh! can you hear it? 

By the way, Neuroendocrine Cancer hates awareness so share to others!

Thanks for reading

Ronny

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Remember ….. in the war on Neuroendocrine Cancer, let’s not forget to win the battle for better quality of life!


 

 

11 thoughts on “Neuroendocrine Cancer – shh! Can you hear it? (…..I didn’t)

  1. Jan guhl April 15, 2016 / 13:40

    Ronnie where would we all be without you. Keeping us up to date with your informative blogs. I have learnt so much from you and send you a big hug and an even bigger THANK YOU!!!!!!!

    Liked by 1 person

  2. Patricia January 18, 2016 / 14:54

    I went in for colovesulcula fistula repair,had two feet of lower intestine removed as well as appendix.. ( no tumor there.they weren’t suspecting any….however Surgeon decided to palpitate my liver, found rice size tumor,removed ,it was a carcinode tumor….had octriotide scan, found no others. Am post menopausal and have occasional hot flash.other than that doing great…glad tumor found, if anything pops up in future have a good base to proceed. Serendipity….

    Liked by 1 person

    • ronnyallan January 26, 2016 / 16:30

      Sounds like you may have had some luck Patricia. Make sure you get good follow ups!

      Like

  3. Paul Cross (@paulcross4) January 4, 2016 / 03:44

    Amazingly Ronny it was a very high suspicion within three days and a definitive diagnosis in I think two weeks for me. However I live very close to Stanford Hospital in California where some of the world’s experts in this disease work. A suspicious GP (or the American equivalent thereof) in my local doctors office (who was actually standing in for my regular doctor) referred me to a surgeon at my local hospital, where I was sent for 3 days for tests. He in turn after consulted with a number of his local colleagues and got me an endoscopic biopsy looked at at Stanford, and I had an accurate diagnosis a few days later. One month and one Whipple procedure at the local hospital and here I am almost 9 years later.

    It’s never been lost on me however that I am almost certainly alive and well due to an accidental consequence of the location at which I live. From diagnosis, to treatment, to ongoing monitoring and care I have interacted with people who know what this disease is and what the latest in treatment options are. Over the years I’ve realized how incredibly lucky I am and how if everyone else had access to this level of care and expertise the outcome for them as individuals would almost certainly be massively improved.

    Therefore the awareness you push for is critical. Awareness will lead to diagnosis, access to treatment, better outcomes and maybe one day a cure.

    Liked by 1 person

    • ronnyallan January 4, 2016 / 08:49

      Great story Paul which I believe is more common than people think (you only hear about the worst cases in media, forums and awareness messages). Technically I was 6 weeks flash to bang but I’m highly suspicious that a colonoscopy 21 months prior to diagnosis was probably the starting point. Thanks for your support here and on twitter.

      Like

  4. Coral November 3, 2014 / 15:00

    Reblogged this on Beyond Life's Challenges and commented:
    Building awareness for this disease is important. Here is an article by a fellow “zebra” living in the UK that is well-worth the read.

    Like

  5. cy October 28, 2014 / 00:37

    So right Ronnie. It took about six years for me to be correctly diagnosed and it was an accident then.

    Like

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