Your NF questions answered directly from the Top!!
04 June 2020
Professor Rosalie Ferner, National Lead for NF1, Trustee and Member of the Nerve Tumours UK Medical Advisory Board
![](/images/common/Rosalie_Ferner2_1024x768.png)
and Mary Thomas, Clinical Neurofibromatosis Nurse at Guy's and St Thomas' NHS Foundation Trust
![](/images/common/Mary_1024x768_2.jpg)
have very kindly agreed to take medical questions from our members, particularly about issues that are concerning you in relation to NF in the current crisis.
They would also like you to feedback your views on how you are finding telephone consultations.
Send your questions directly to info@nervetumours.org.uk
Please remember that they cannot answer any particularly personal medical questions, but if you do have any major and immediate concerns please call the Nerve Tumours UK National Helpline on 0793 046030 that is operating each working day at present.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Connection_Coalition_370x280_800_600_s_c1.jpg)
Connection Coalition
NTUK joined the Connection Coalition with the aim of working together to build strong relationships & connected communities
Read More![](https://nervetumours.org.uk/images/made/images/common/Rare_Disease_Festival_Website_preview_370x280_800_600_s_c1.jpg)
Rare Disease Day 2021
Nerve Tumours UK joined events showcasing Rare Disease Day hosted by the Genetic Alliance on 28 February 2021
Read More![](https://nervetumours.org.uk/images/made/images/common/NF1_Mummy_image_1_370x280_800_600_s_c1.jpg)
Kate, NF Mummy Community & Support
Kate tells us why she started the NF1 Mummy community group online
Read More![](https://nervetumours.org.uk/images/made/images/common/Alex_2-edit_preview_image_800_600_s_c1.jpg)
Alex’s story - Support in the Workplace
Alex Hetherington shares how iNForming his work colleagues about his neurofibromatosis created a supportive work environment
Read More![](https://nervetumours.org.uk/images/made/images/common/adam-whitlock-I9j8Rk-JYFM-unsplash_preview_800_600_s_c1.jpg)
A Colourful 5K Challenge
Read Emma's incredible awareness raising activities for NF in her local community, Liverpool.
Read More![](https://nervetumours.org.uk/images/made/images/common/Courtney_Garden_Marathon_World_NF_Day_2_preview_800_600_s_c1.jpg)
Our NF community share why they are taking on the World NF Day: 2.6 mile Garden Challenge!
Taking part in the World NF Day: 2.6 Garden Challenge - We want to hear from you!
Read More![](https://nervetumours.org.uk/images/made/images/common/Genomics_Showcase_preview_800_600_s_c1.png)
Nerve Tumours UK takes part in the Genomics Showcase
Find out how you can take part in the Genomics showcase – sign up for free!
Read More![](https://nervetumours.org.uk/images/made/images/common/Website_header_370x280_800_600_s_c1.jpg)
Kate “NF1 Mummy” Your Questions on parenting answered: World Neurofibromatosis Day 17 May 2021
Have you got questions about your child’s NF diagnosis? Send them into us for World NF Awareness Day
Read More![](https://nervetumours.org.uk/images/made/images/common/Jo_160_mile_fundraiser_preview_800_600_s_c1.jpg)
Jo’s 160 Mile walk for NTUK!
Read Jo's Story as she prepares to take on a 160 mile epic walking challenge for Nerve Tumours UK.
Read More