NETwork with Ronny © – Community Newsletter OCTOBER 2017

Hi NETworkers!

Welcome to Ronny Allan’s Community newsletter for October 2017.  A very strong end of the month due to massive support for my Halloween themed but very serious and hard-hitting post “Neuroendocrine Tumors – no treats, just tricks”. If you’ve not seen it or commented on it, check it out here on the Facebook site.  I suspect the number of shares will never be beaten (652 in 36 hours).  31 Oct 2017 is now the biggest number of views on any one day, breaking the previous record set in Jan 2017.  It also made October 2017 the highest monthly views ever.  I am so grateful to those who made that happen ♥

What’s in the NET News

The following news items may be of interest:

  The huge (but expected) news that Novartis Novartis (manufacturers of Octreotide) is purchasing Advanced Accelerator Applications (AAA) (manufacturers of Lutathera Lu-177 (as used in PRRT)). This is a significant acquisition and should benefit the NET community given the size of Novartis and the potential of PRRT worldwide. It will be interesting to see if this has an impact on the UK approval

Read more here.

  I wasn’t at NANETS but did check most of the output consolidated into this post – Read more here
  GA-68 PET (NETSPOT) continues to roll out across the USA, see CCFs latest list by clicking here.
Made it to 3 finals in the WEGO Health awards, I posted about this  here.

Blog Site?  

Due to the vagaries of Facebook inner workings, some of these may not have even shown on your timeline.  So, ICYMI …….here’s a summary with links, includes updated blogs. You can actually sign up to receive my blog articles direct to your inbox when published – subscribe here.

 Neuroendocrine Cancer – Trick or Treat.  This ‘themed’ post generated a huge amount of sharing, breaking all previous records.  See more in the newsletter.
  A summary of NET stuff from NANETS 2017
 “You’re Cured” – Topical and controversial in NETs. My opinion.
Weight can be an issue in NETs.  It did actually trigger my diagnosis.
The shock effect never wears off.  My private messages are full of disturbing stories, not just about diagnostic issues but support and care received.  A new campaign.
Genetics and NETs.
My first article for Cure Magazine “It’s not all about me” 


Other Activity

October was a busier month in terms of blogging despite several personal challenges and external projects on the go.  Striking a balance remains difficult, I’m keen to support and advocate but as a patient, I also need my own time.  I still managed to break 2 records in October, mainly due to my Halloween themed post on 31st.  The biggest amount of view in any one day had stood since Jan 2017 and was totally smashed, as was the best month too.   Thank you all so much for the support.

Please join my 2017 awareness campaign event here (select ‘Going’)

I continue to receive a steady flow of private contacts, mainly from patients seeking information.  I don’t have an issue with private contact but please note my disclaimer.  Please also note that I cannot accept telephone calls on a one to one basis.  Also, the number of non-patients contacting me for other reasons (mainly to help with something) continues to grow and this is producing some great publicity and awareness.

Awareness Activity in October 2017

New Audiences for NET Cancer.  From Day 1, I said it was my aim to find new audiences for NETS rather than just share stuff within our own community. I’m doing this!

  • Article features.
    • Cure Magazine.  I’ve been accepted as a ‘Cure Today’ contributor which means my articles will get a wider distribution than they do now.  Cure Magazine has a readership of 1 million.  Click here to read more. In October, I was featured in Cure Magazine twice:
“Cancer isn’t all about me”
“Poker Face or Cancer Card”
  • Twitter. I took part in a WEGO Health patient leader chat on twitter where I was able to contribute to some general cancer questions (subject chronic illnesses).  It was attended by many patient advocates representing many different conditions. The taking part in these activities is time-consuming and mentally hard work but it does allow me to grow as a general patient advocate and to occasionally mention “Neuroendocrine Cancer” spreads awareness to new audiences!  A summary of the conversation can be found here.
  • I’m ‘extremely’ active on twitter and I find a lot of my research stuff there. I also use it to support other conditions and it’s mostly returned (i.e. others help with NET awareness and are made aware of NETs in the process).  In Oct, I tweeted 218 times on my personal account which lead to almost 89,000 views.  I was mentioned 160 times by other tweeters and gained 49 new followers.  My tweet “Ignore this post” remains the most tweeted article about NETs ever posted on twitter.  Check it out – click here.


  • Daily Newsletter from my twitter feed (Nuzzel).  There is so much on twitter that I could swamp the community Facebook site so I started a twitter newsletter via an app called Nuzzel which seeks out stuff I normally like. Click this link and sign up if you think this is something you’d be interested in receiving – you don’t need to have a twitter account to read, just sign up with an email.  Currently 374 subscribers – up 11% on last month.

  • WEGO. I continue to be featured by ‘external’ organisations such as WEGO and my PODCAST is reaching new audiences – click here.  The recent awards will continue to showcase my work which has the effect of spreading Neuroendocrine Cancer awareness to NEW audiences in addition to enriching my experience as a Patient Leader.  WEGO is a fantastic organisation!

  • Macmillan Cancer Support.  I’m proud to be a ‘Voice’ and ‘Community Champion’ on the Macmillan Cancer Support Forum.  In addition I help ‘outliers’ from the NET community there. There are only 27 champions for a site supporting hundreds of thousand patients – it’s a community of communities.   This is the biggest cancer support organisation in the UK and I’m intent on developing relationships with various departments in this fantastic organisation.  They have recently agreed to feature NETs on 10 Nov 17 and I’m writing an article in preparation.
that’s me in the centre

Speaking Engagements

  • I was delighted to speak to the South Wales NET patient group (sponsored by NET Patient Foundation).  Here’s some pictures of Chris and I with the group and the local NET Specialist. Dr Mo Khan is setting up a brand new NET Service in Wales – great news for this group.
Left to right: Nikie Jervis (Nurse from NET Patient Forum), Sally Jenkins NET Cardiff, me, Yolande Mears NET Swansea, Chris (my wife)
Dr Mohid Khan – NET Specialist Wales – great supporter of my blog and NET patients Quality of Life
  • On 16 November, subject to contract, I’ve been invited to speak for around an 45 minutes at an Ipsen sponsored NET Nurse event in Birmingham. Tough gig!  Post to follow if allowed by contractual arrangements.

Writing and other types of Engagement (external) – watch this space as I’m working on quite a few projects concurrently.  I’m currently in a pool of patients who may be featured in a UK national, fingers crossed.  Writing an article for Macmillan on NET Cancer Day.

Social Media and Stats

Blog Milestone.  In October, I accelerated past 400,000 views! Thank you all so much Keep sharing!  On track for half a million by Easter 2018.

Facebook Milestone.  I would love to achieve 6000 followers by the end of 2017 but this will be a challenge.  The Facebook page is now my biggest outlet for awareness and education so please please please recommend this page to anyone you think would be interested.

Also check out my sister Facebook sites here (go to these pages and click on ‘Like’)

These are fallback  sites to counter the Facebook algorithm whereby you may not see all my posts on the main site (click on the links to see the pages)

Ronny Allan’s Community

Neuroendocrine Cancer Awareness and Networking


I’m expanding into Instagram to see how that goes. I’ve amassed over 230 followers to date. Initially, I’ll just be posting pictures of things that inspire me, mostly scenic photos of places I’ve been or want to go!  You can follow me here:  Click here to go to my Instagram page

Community Statistics (the measurement of my efforts on your behalf)


  • Facebook 5337.  This is a key outlet for my blog – please encourage others to like my page (if you’d like to know how to use your Facebook to invite others to my page – let me know, I can provide you with a step by step approach).
  • Twitter4202 / 3252 Follow me here @RonnyAllan1 / @NETCancerBlog


Neuroendocrine Cancer – no treats, just tricks
Neuroendocrine Cancer – Tumour Markers and Hormone Levels 
Living with Neuroendocrine Cancer – Home Page
Steve Jobs – the most famous Neuroendocrine Cancer Ambassador we NEVER had
Diagnosed with Neuroendocrine Cancer? – 10 questions to ask your doctor
Background to my Diagnosis and Treatment

WOW!  – that’s an amazing amount of awareness and hopefully, support for others.  However, I cannot do this without you guys liking, commenting and sharing!  The likes give me motivation, the comments (and private messages) give me inspiration (or at least a chance to explain further) and they also keep me humble.  The sharing gives me a bigger platform.  A bigger platform generates more awareness.

Thanks for your great support in October.  Onwards and upwards!

Thanks for reading


I’m also active on Facebook.  Like my page for even more news.  I’m also building up this site here: Ronny Allan


My Diagnosis and Treatment History

Most Popular Posts

Sign up for my twitter newsletter

Remember ….. in the war on Neuroendocrine Cancer, let’s not forget to win the battle for better quality of life!


4 thoughts on “NETwork with Ronny © – Community Newsletter OCTOBER 2017

  • Deanna Vickery, Mrs

    Dear Ronny. I hate to ask a man who’s already working 26hours per day, but I need your help. I’ve forgotten which issue it was in, but stated that medical circles are going to re-name pituitary adenoma as it’s now accepted as being a NET cancer. I would like to print this off to show my endocrinologist this month: she has always said that she is only intrested in making sure my Cushings isn’t coming back ie p-adenoma growing back. She reckons it has nothing to do with my midgut NET.
    I need to spread awareness here!
    Can you help please?

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