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

Specialist Neurofibromatosis Nurse - Wales
Find out more about our latest position available in Wales
Read More
Covid-19 Impact on Wellbeing in Families of Children with Rare Neurogenetic Disorders (CoIN Study)
Find out how you can get involved
Read More
Julie Ann Evans
Learn how to navigate the benefits system for people with NF & how to approach Personal Independence Payments (PIP)
Read More
Katie’s Story
Read Katie's inspirational NF Story & how she uses running to overcome her problems
Read More
#OneMoreNurse
We need your help to continue our Specialist Neurofibromatosis Support Network
Read More
NF1 Army’s incredible 10 million steps fundraiser!
read about team 10 million steps fantastic lockdown fundraising efforts
Read More
Billy & Logan’s Story
Read about how engaging in sport supports them both with NF1 related issues
Read More
The One Show Year Book in Lockdown
Jacob & Ella take part in The One Show's Nationwide Yearbook for students in secondary school
Read More
Benefit and Financial Support Matters answered by our Specialist
Find out how you can get your disability benefits and financial support questions answered
Read More