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Ronny Allan
Today – the following figure is the total number of views of my blog! Can you help me get to 3 million?
- 2,425,332 views
Today, 27th October 2022, I can confirm the 2 million views milestone has been reached.
I was totally astonished to have been able to accumulate a million views of my blog around the middle of June 2019 and in December 2020, a Christmas present of one and a half million! Fast forward to November 2021 and it’s one and three-quarters million.
That is THANKS to you guys for reading and sharing.
When I first set up this blog in Apr 2014, it was just to help spread awareness (and collect a few pennies) whilst I was walking the 84 miles of Hadrian’s Wall with my wife Chris. I never thought for one minute I would reach a thousand hits let alone 2 million: whilst accumulating around 20,000 followers across all my social media sites.
Will I aim for 3 million? I will leave that up to you, my readers. THANK YOU!
My key aims are international-level awareness, advocacy, campaigning, and support for all Neuroendocrine Cancer patients via all my social media accounts. I’m not your regular Neuroendocrine Cancer advocate and I do things differently rather than follow the crowd. I’m certain that fact has played a part in getting to this stage.
People often ask me how I’ve been able to build up my sites and it’s a tricky question because I’m not sure what happened! I just put my head down and attacked the task in my usual tenacious way – so I guess that’s part of my subconscious and inbuilt strategy. I did author an article about my blog journey for WEGO Health for those interested – read here. I’ll approach WEGO Health (now Health Union) to see if they wanted to update this to 2 million!)
My blog is central to my activities and through this medium and some others, I’ve really invented my own brand of Neuroendocrine Cancer awareness. I pride myself on being an international and independent writer which allows me the freedom of movement I need. So far, I’ve managed to win THREE international awards breaking through into new areas for awareness. It’s difficult for a Brit to win in what is essentially a US awards programme. In 2016, I won the WEGO Health Best in Show Community plus a finalist in another category, made it to 3 finals in 2017/18, and then won Best in Show Blog in 2018. I took a break from entering these words in 20-19/2020 but in 2021 I was in 2 finals and won the Lifetime Achievement award. You can read my WEGO history here.
Other Advocate Activities
I don’t just write a blog! I’ve also spoken at many events and to pharma/healthcare-only audiences including Ipsen Global Paris, Ipsen UK, Ipsen Germany, Ono Pharma UK, Royal Marsden Hospital, Eye for Pharma London 2018, EUHIC Berlin 2018, Society and College of Radiographers. I’ve also presented to a few UK and overseas patient groups, including the UK, Scotland, Wales, Canada, New Zealand, South Africa, and the Middle East. You can see some of those talks here.
I’m also a contributor to Cure Magazine although only two articles published to date (soooooo busy!) – but read those here.
Other invitations include the making of an educational video for Lex Pharma, helping to create and featured in Ipsen‘s patient support website Living with NETs, a photo shoot for a Macmillan Cancer internet campaign (click here), a photo and video shoot for Ipsen as a member of the European Pharmaceutical Industries and Associations (EFPIA) (click here). I’ve also been featured and/or mentioned in numerous other locations – read my blog site home page to read more.
Board Membership
Member of the following boards:
- 2019 WEGO Health Patient Advisory Board – click here to see my WEGO profile.
- ONO Pharma UK Patient Advisory Board (now disbanded).
- Multi-Med Inc Strategic Advisory Board – click here.
- Ipsen Patient Advisory Board for their Living with NETs website.
- 2022 WEGO Health Patient Advisory Board (Health Uni0n) – click here to see my WEGO profile.
Patients Included
Everything I do is about patients and my site is accredited as “Patients Included“. That means everything must have patient input.
Disclaimer and Disclosures
All information provided on any of my social media accounts does not constitute professional medical advice. See my disclaimer and disclosures here.
My main sites are here (be careful not to unfollow or unlike!):
Blog – RonnyAllan.NET – Click here
Twitter – @ronnyallan1 and @neuroendocrine
Facebook – Here are the main 3:
- Neuroendocrine Cancer – my main site with over 11,000 followers as of Nov 2021) – click here and ‘Like‘ the page (BUT don’t unlike!)
- Ronny Allan – additional output, more personal stuff – click here and ‘Follow’ (BUT don’t unfollow!)
- World Neuroendocrine Cancer Day – my own version of the current misnomer day posting awareness 365 days per year. Click here and ‘Like‘ (BUT don’t unlike!)
Newsletter – extending the reach into wider areas via a bi-monthly newsletter from twitter, my website, facebook, google alerts and other sources. click here to subscribe.
Instagram – click here to follow (mainly supporting my Ronny Allan Facebook page
YouTube – click here to subscribe (mainly supporting my Ronny Allan Facebook page but also contains some of my video presentations)
Private Facebook Group (Educational focus) – I also have a private Facebook group which is the largest and the fastest-growing group in the NET community – click here to join (don’t forget to answer the questions).
Message me here: http://m.me/RonnyAllanBlog
Many of you who read this will already be on these sites so please ‘Follow’ or ‘Like’ as appropriate – be careful you don’t ‘Unfollow’ or ‘Unlike’. Please don’t send friend requests to my personal profile, I need that for my ordinary life!
There are so many other sources of routes into my blog and I’m grateful to the many patient advocate organisations, patient advocates,patients and caregivers, and even the healthcare community; who provide some of these routes in. If you’re reading this, thank you so much.
Please also note:
All information provided on any of my social media accounts does not constitute professional medical advice. See my disclaimer here: DISCLAIMER
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.
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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
Please Share this post for Neuroendocrine Cancer awareness and to help another patient
Discover more from Ronny Allan - Living with Neuroendocrine Cancer
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Thoughts on TACE treatment…I would like to hear if anyone has had and their experience. I’ve been diagnosed w Carcinoid Tumor Colon w Liver Mets or well differentiated Neuroendocrine Tumor. I’ve had section of colon removed, Y-90 Treatment recently to my liver and I am now trying to get approval for TACE. Like most of your posts I too have had gastro experience for many years believing I had IBS and flushing thinking I had an allergy,
I had a battle w kidney stones for a few years now and my most recent sent me to hospital to find out I had a large NET in my colon (after spending 5 hours in ER an MRI, CT Scan and Ultrasound, and a second Radiologist diagnosed it five mins prior to me leaving the hospital) and was told I had cancer. It’s been 6 mos Now. My oncologist wants me to begin injections once my treatment is complete and Tumors are shrunk or gone. I feel like I’ve been on some wild roller coaster ride, No one tells you what to expect or can really understand, so thank you for all you do Ronny and all who are posting.
Thanks Julie, this has come through on my blog site, do unlikely to get a response other than from me. If you wanted to hear from people who’ve had TACE, you need to post in my private Facebook group.
Hi Ronny, lm just reaching out – in a predicament over my husbands treatment plan. He had a pet scan and bloods taken in January, it was given the all clear to have PRRT. His recent blood tests show low platelets, but rising. It was suggested that the pet scan was responsible. They have now said that actually, due to the amount of cancer he has in his liver, they are reluctant to give any PRRT. Surgery is now being discussed, which has been ruled out in the past 3 years as being too risky. We have lots of specialists discussing us at the moment. He has had streptazocin and everolimus, which he reacted very badly to. He had PRRT three years ago which really worked. He is healthier than he was back then. Our issue is that if the liver is operated on it is a three month recovery. What happen to the cancer in the pancreas and bones. It is very frustrating to say the least, because of the initial decision being changed.
This is complicated, but l wanted to hear the thoughts of some one that understands.
Many thanks
Lisa
sorry your hubby has had to go through all that, you too. This is a tough question. There is multiple treatments involved and sequencing adding to the platelets issues. As you said, it’s complicated. Lets take my own experience. My liver tumours were slightly more aggressive than my primary (small intestine). I had surgery with a very experienced liver surgeon, he took out 66% of my liver, it kinda grows back. I still have some tumour deposits. My Chromogranin A (tumour bulk) didn’t reduce until liver surgery (my primary was removed 4 months previously). I’ve never had PRRT but I do know it’s a good treatment and works for most. I still don’t understand some of the intricacies of it though, in terms of risks, except I know renal issues can be. I’m guessing he’s Grade 1or 2 ?
No?
I just got likes and comments from ‘Crystal Tipps’. Coincidence!
I was intrigued so checked, and there are a few Crystal Tipps on FB, one with a connection to NETs, what a strange coincidence indeed!
[…] Ronny reaches half a million views […]
[…] Ronny reaches half a million views […]
I very much appreciate what you do, Ronny. We have reposted some of your stories on our new PRRT SEATTLE Facebook page. We are trying to get the word out to patients that PRRT is available now for our disease. I am the first person in Washington State to get PRRT. Am currently half way through my treatment. Keep on getting the word out there!
Any issues with insurance?
[…] Ronny reaches half a million views […]
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Well deserved👍🏻
Have you got a new facebook account?
No?
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