Another great start to 2023 and I thank those who continue to support my social media and this blog. I’m keen to hear any suggestions of the sort of thing you would like me to research and publish. I am working on two or three more blog posts due to come in in the next 10 days, please stay tuned.
The top 10 most-read posts in February are listed below:
This is not a surprise, it’s one of my top 6 ever but it got a good read last month. It’s the first thing people should ask at diagnosis. If this floats your boat – Click here or on the picture.
My new format of newsletter (via my blog site) looks like it was successful. Click here or on the picture.
If you need a catch-up, this is the place to go. It updates what is being read most on my website in the last 48 hours and automatically updates. No surprises on its inclusion, I do market it a lot.
Click here or on the picture to read more.
This got an amazing reception when I shared it in February with viewings steady over a 4-day period indicating many shares. I thank you for supporting it.
Click here or on the picture to read more.
The heterogeneous nature of Neuroendocrine Neoplasms must be understood to avoid confusion and chaos in patient groups. That was my thinking when writing this article. It’s also a great awareness piece. Click here or on the picture to read more.
This got a wonderful response indicating it was shared many times. Perceptions of cancer can sometimes be wrong. Click here or on the picture to read more.
I was surprised to see this do as well as it did, Gastric NETs are not the most common type.
Click here or on the picture to read more.
A frequently visited post, very helpful I’m told. It will one day be my most-read blog post. Click here or on the picture
Great response for this post – many thanks. Click here or on the picture to read more.
A frequently visited post, very helpful I’m told. The cause of fatigue is so difficult to pin down, but this blog has links to experts in Cancer Related Fatigue. Click here or on the picture
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 as they are not members of the private group or followers of my sites in any official capacity. 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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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
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