Translate
Ronny Allan
Every year I cast my mind back to this time in 2010. Diagnosed on 26th July that year, I was in hospital from 8th – 26th November, an extended period due to complications. At that point, I had been keeping my diagnosis within close family and friends and my manager at work. People at work and my wider list of friends were probably wondering what was going on with me.
Cleary, I let my emotions slip by posting this on my personal Facebook profile on 20th November 2010. Perhaps this was my way of opening up. To be honest, the first few days I was suffering a lot of fatigue and brain fog from the morphine/painkillers. The thought of posting stuff on Facebook was far from my thoughts. I was receiving newspapers from day 3 but could not even focus for more than a couple of minutes. Then on 20th November 2010, I got hold of my tablet and typed “Feeling perkier”. It was a milestone.
That was 11 days after the surgery, so I guess it took a while to feel almost normal. I had a big surgery! I had some issues along the way. But after 10 days I had got through these issues with the help of the doctors and nurses and felt stronger, the light at the end of this particular tunnel was shining brighter than ever before.
By the time I wrote about that experience on 17th November 2015, some of the detail had gone. I also tried to write about it with some amusing recollections. I do laugh about some of it, particularly:
1. the suppository story,
2. the moving picture when I was on the PCA (pain control),
3. the refusal to do physiotherapy one day,
4. the urine bag leak on the CT scan.
In hindsight, I wish I had kept a diary of some sort covering the whole period. There are no pictures of machines or me with tubes etc, that is not my style.
To say there wasn’t a time during those 18 days when I was scared would not be truthful. I once got a message from someone who said, after reading my surgery experience article, that it scared her. I’m so sorry that person was scared, I don’t want to scare anyone, I wanted to tell my story the way it happened but at the same time provide hope given that it was such a long time ago and I feel fine.
Check out my 2010 surgery Parts 1 and 2 below:
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.
Top 10 Posts & Pages in the last 48 hours (auto updates) (Click the titles to read them)
Thanks for reading.
Personal Facebook. Like this page please.
Blog Facebook. Like this page please.
Awareness Facebook Like this page please.
Sign up for my newsletters – Click Here
My Diagnosis and Treatment History
Check out my online presentations
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
‘Chinese Dumplings’ and Neuroendocrine Cancer
Update of one of my posts from 2015 which was interesting in that year. This is not really about a treatment which is available everywhere
“An odd disposition of tumours” – less common metastases in Small Intestine and Pancreatic NETs
Every day is a learning day in NET! When I was diagnosed in 2010, my Oncologist sent me for a specialist scan that would help
Chemotherapy for Neuroendocrine Cancer
Edited and checked April 2024One of the unusual aspects of Neuroendocrine Cancer is that chemotherapy is not normally considered as a ‘standard of care’ or
Carcinoid vs Neuroendocrine
OPINION – There’s a constant debate regarding the validity of the term ‘Carcinoid‘. I’ve posted about this a few times and as far as I know,
Things are not always how they seem
Graphic courtesy of SoBadAss.me (Sam Cleasby) In 2014, Chris and I walked 84 miles along Hadrian’s Wall on the English/Scottish border. It was a fantastic
Neuroendocrine Cancer Online Forums: frighteningly good or good at frightening?
OPINION When I was diagnosed, I was happy with my own research and kept away from forums on the advice of a fellow patient who
Colonoscopy Comedy
Last year I wrote a series of articles on the ‘coping’ side of cancer, one of which was about still being able to have a
Surgery – the gift that keeps on giving
I first wrote this article in December 2014. My thoughts went back to my first surgery in 2010 when I was discharged 4 weeks before
Piss off cancer, it’s 13 years since my liver surgery!
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
Related
Discover more from Ronny Allan - Living with Neuroendocrine Cancer
Subscribe to get the latest posts to your email.
I wanted to thank you for recommending Dr. Star in Jacksonville. He is great. I did tell you your article terrified me, but, I still needed to know what your experience was. Luckily my experience was not so traumatic and I have come out the other side with a great prognosis. I told Dr Star you recommended him and he said to thank you, he loves you and highly recommended all your writings and blogs. Thanks again for all you do.
Lori V.
thank you, best wishes for your recovery and ongoing health