Piss off cancer, it’s 12 years since my liver surgery!

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I’m still here

I was 54 years and 9 months old at diagnosis on 26th July 2010.  For the first few months, I had no idea what the outcome would be.  What I did know at the time, given the final staging, grading, and other damage that was accumulated via various tests, checks, and scans; is that my body had been slowly dying

Without intervention I may not be here now to tell you this tale and who knows what would be listed on my death certificate.  It’s amazing to think something that would eventually kill me without intervention, didn’t have a much grander announcement than the one presented to me in 2010 (or had I been paying more attention, in 2008 or 2009). I will never know if a much grander announcement would have happened because following my chance diagnosis, I was ‘patched up’ and thankful to still be here today. 

My second big surgery took place on 12th April 2011.  This was around 5 months after major abdominal surgery to remove the primary tumour in the small intestine plus some loco-regional stuff.  This second surgery was now to address my tumour metastases.   

Truthfully speaking, I did not expect to be here writing this in 2023, or at least that was my thinking at the time and for some years after that.  The fact that I am must be related to the early intervention and radical surgery administered 2010-2012 and constant surveillance since, perhaps Lanreotide too. As a metastatic small intestine NET, debulking surgery is thought to be prognostically advantageous for many.  

Accessing a specialist team is important early on, preferably before surgery as there are certain vagaries with Neuroendocrine Tumours (NET) which should at least be considered.

The surgical experience

I’ve written extensively about this, and you can read my liver surgery experience here:

Click to read about my liver surgery experience

Now revise my first surgery to remove the primary and other stuff:

Click on the picture to read
Click on the picture to read

A lot happened ……..

Check out my detaile clinical history from diagnosis on 26th July 2010:

Click on the picture to read

I try to piss my cancer off! 

Click to read

I thought I was going to die …… I DID’NT

Click to read more

I’m still here

Click to read more


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.

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A cup of tea

I would also mention those who contributed to my “Tea Fund” which resides on PayPal.  You don’t need a PayPal account as you can select a card but don’t forget to select the number of units first (i.e. 1 = £4, 2 = £8, 3 = £12, and so on), plus further on, tick a button to NOT create a PayPal account if you don’t need one.  Clearly, if you have a PayPal account, the process is much simpler 

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This screenshot is from every single post on my website and depending on which machine you are using, it will either be top right of the post or at the bottom (my posts are often long, so scroll down!)

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