#NeuroendocrineCancer #NETS #PatientVoice PatientAdvocate
RonnyAllan.NET – Community Newsletter Covering August 2018
Ronny has been busy again, as always with his amazing work as a patient advocate which you can read about in his latest Community newsletter.
Ronny also shares the latest up to date information regarding Neuroendocrine cancer, or NETS for short, and there are lots of things to read regarding upcoming activities too, as well as a personal update.
I’m looking forward to meeting Ronny in London in October, and also to hearing him present at the 15th Annual eyeforpharma Patient Summit, where he is co-presenting with Ipsen.
WEGO award winner Ronny is also through to the final again this year for a WEGO award so GOOD LUCK RONNY from all at FibroFlutters 🦋💜🦋
You can read Ronny’s latest Community Newsletter via this link >>>
International Awareness of Neuroendocrine Cancer and associated issues.
Supporting and helping NET Patients
Header image by Cancer Research Uk >>>
About neuroendocrine tumours (NETs)
Find out about the neuroendocrine system and what neuroendocrine tumours are.
FibroFlutters – Support Group for people with Fibromyalgia, Chronic Pain, EDS/Hypermobility, Mental health, Chronic fatigue/Me, Rare & others offering friendship, support & advice in Sunderland, NE UK and across the globe
Please can you read our Disclaimer & Privacy notes and if you have a problem we are always open to discussion, just e-mail Carole email@example.com
Advocating for a Multi-Disciplinary approach to all aspects of medical healthcare. With a model approach using all the ‘stakeholders’ I’ve designed a patient’s perspective of what patient-centred care, patient-included, patient-involved, patient-centric should look like and involve, that’s everyone by the way!
You all need to pitch in!!
2 thoughts on “#NeuroendocrineCancer #NETS RonnyAllan.NET – Community Newsletter Covering August 2018 #PatientAdvocacy”
thanks for featuring me!
Always a pleasure 🙂
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