Self Pity or Self Help?
I’m not one for wallowing in self-pity or accepting invites to pity parties. It’s not my style. Things happen in life, and some are impossible to undo so I want to get on with my life in the best way possible. To some of you, that may sound harsh and insensitive, but I don’t lack empathy for others (my advocacy work is a testament to that) and I’m constantly sympathising with others in my quest to help them via my blog, Facebook pages, and private Facebook group (see green box below) which is the biggest in the world because I’m known for helping. I admit that some people are beyond my type of help, but I always suggest they should speak to specialists in the area where they need the help. My disclaimer looks after most scenarios. p.s. I don’t like having a disclaimer as I’m a genuine person, but it was advice I took some years ago.
I’ve written many blog posts on this subject. I even suggested to an ENETS conference panel that this was an unmet need because many NET patients having been diagnosed late and undergone treatment, need help because it often means a reduced quality of life. At least one doctor (a NET specialist) seemed to take umbrage at my suggestion. However, when I look at some of the output from the national NET organisations/foundations, it would appear I was not alone in suggesting that more help is required to support people post-diagnosis/treatment.
On the Cancer Journey, don’t forget to live your life
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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European Neuroendocrine Tumor Society (ENETS) 2023 guidance paper for Digestive Neuroendocrine Carcinoma
This ENETS guidance paper, developed by a multidisciplinary working group, provides up-to-date and practical advice on the diagnosis and management of digestive neuroendocrine carcinoma, based
European Neuroendocrine Tumor Society (ENETS) 2023 guidance paper for gastric neuroendocrine tumours (NETs) G1–G3
The ENETS 2023 guideline for gNETs are combined with the guidelines for Duodenal NET (dNET) due to their close relationship in anatomical terms. Gastric neuroendocrine
European Neuroendocrine Tumor Society (ENETS) 2023 guidance paper for Duodenal neuroendocrine tumours (NETs) G1–G3
The ENETS 2023 guideline for dNETs are combined with the guidelines for Gastric NET (gNET) due to their close relationship in anatomical terms. But there
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
Another episode in the expert opinion series. I thought this might be useful for some of you after an interesting ‘google alert’ brought up these