Postponed: Medicine and Me: Living with Nerve Tumours at the Royal Society of Medicine
13 March 2020
We would like to update you regarding the Medicine and Me: Living with nerve tumours event that was due to take place at the Royal Society of Medicine on Thursday 23 April 2020. Unfortunately due to the current Coronavirus (COVID19) situation and the lockdown restrictions in place, The Royal Soceity of Medicine has decided to cancel any in person events taking place in July 2020.
As such the Medicine and Me: Living with nerve tumours meeting due to take place on Monday 13 July 2020 has now been postponed. Currently there is not a new date set, however this will most likely be in early 2021. The Royal Society of Medicine will be in contact with ticket holders directly in due course and tickets will be valid for the to be agreed later date. We will keep you posted on any further developments.
Medicine and Me: Living with Nerve Tumours
Postponed until further notice
The Royal Society of Medicine
1 Wimpole Street, London
Nerve Tumours UK and The Royal Society of Medicine invite you to attend a half day conference highlighting and discussing Neurofibromatosis.
The country's leading experts in Neurofibromatosis Type 1 and Type 2 will review and discuss current approaches to diagnosis and treatment, in the light of advances in molecular biology and imaging. There will be patient presentations and a panel discussion.
By attending this meeting, you will have the opportunity to:
- Understand the epidemiology, biology and genetics of Nerve Tumours - Neurofibromatosis I (NF1) and Neurofibromatosis 2 (NF2)
- Appreciate the impact of living with NF1 and NF2 first-hand from patients
- Learn about the recognition of malignant transformation (NF1)
- Discover the management of NF2 nerve tumours
- Explore today’s treatments
- Understand the management and support for people with Neurofibromatosis
About Medicine and Me
Medicine and Me meetings aim to provide an outline of current best practice and future updates of important conditions and to give direct voice to patients and their carers and enable them to discuss their concerns and reflections on the impact of diagnosis, investigation and management.
Physicians and surgeons and indeed all healthcare professionals continue to learn from and be inspired to greater efforts to improve care by hearing directly from patients.
The Programme and tickets, free of charge for patients, carers, relatives, students and trainees are available on the link below:
BSL Translators will be in attendance, and for any further special access or specific needs, please email us at info@nervetumours.org.uk by 31 March 2020
Filter News

Freddie’s motto: Be kind, be brave and be happy
Meet Freddie: diagnosed with NF1 as a baby, he loves performing and has a role in soon to be released film Christmas Karma
Read More
Understanding Neurofibromatosis Type 1 (NF1): A surgeon’s thoughts
Christopher Duff is a plastic surgeon working with NF1 patients in Manchester, he answers some common questions from patients
Read More
Understanding NF1: A guide to skin neurofibromas and their treatment
This guide is for people with NF1 and explains what neurofibromas are and what treatments might help.
Read More
Revisiting the GCSE class of 2020
Five years on from their GCSEs, we speak to Ella, Thomas and Noah to discover what they have been up to
Read More
Benjamin’s NF1 story
11 year old Benjamin has NF1 and is the inspiration for his family's fundraising
Read More_3_800_600_s_c1.jpg)
Lynne Highy joins our team of Specialist NF Advisors
Read all about the newest addition to our team.
Read More
NF Academy 2025: Georgia’s Blog
NTUK ambassador Georgia Baum shares her transformative experience of attending the NF Academy 2025 in Barcelona
Read More
Craig’s story
Craig describes his mosaic NF2 related hearing loss, and how a cochlear implant & hearing aids have changed his life
Read More