Changing Faces Impact of Covid Survey
26 January 2021
Due to the Covid19 crisis, we know that many people with visible difference are self-isolating and trying to stay at home wherever possible. With another lockdown upon us and the return to work and social situations looming, many of you are feeling increasingly anxious about the current situation.
That’s why if you or a loved one has a visible difference; Changing Faces want to hear from you. Share your experiences of the current pandemic and help to improve support now and in the future for people with visible difference. Positive or negative or a mixture, it’s important to share. The survey takes only 5-10 minutes to complete and is a big help to our community.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Nimo_NF1_Story_370x280_preview_800_600_s_c1.png)
Nimo’s NF1 Story
Read Nimo's incredible journey of coming to terms living with NF1 & how Nerve Tumours UK has changed her life for the better
Read More![](https://nervetumours.org.uk/images/made/images/common/Georgia_Schwannoma_Story_370x280_800_600_s_c1.png)
Georgia’s Schwannoma Story
Read Georgia's inspirational Schwannoma story and how she had to fight for her diagnosis
Read More![](https://nervetumours.org.uk/images/made/images/common/Screenshot_2020-09-30_Changing_Faces_»_New_research_on_experiences_of_men_with_visible_differences_370x280_800_600_s_c1.png)
Voices of Visible Difference #YoureNotAlone Men’s Campaign
Two-thirds of men with visible difference are affected in their day to day life. Read more
Read More![](https://nervetumours.org.uk/images/made/images/common/Childhood_Neurological_Conditions_Survey_Website_Header_370x280_800_600_s_c1.png)
Childhood Neurological Conditions Survey
Find out how you can help shape the future of treatment for Childhood Neurological Conditions such as Neurofibromatosis
Read More![](https://nervetumours.org.uk/images/made/images/common/Karen_Portrait_Colour_370x280_2_800_600_s_c1.jpg)
We’re Here for You, Our NF Community.
A big thank you from Karen our Charity Director - your support has been amazing!
Read More![](https://nervetumours.org.uk/images/made/images/common/Global_Genes_Virtual_event_370x280_800_600_s_c1.jpg)
Global Genes LIVE!
Join Global Genes September 15-25, 2020 at Global Genes LIVE! A RARE Patient Advocacy (un)Summit.
Read More![](https://nervetumours.org.uk/images/made/images/common/Disorder_channel_promotion_370x280_800_600_s_c1.jpg)
Shine A Light on Neurofibromatosis now streaming on The Disorder Channel
Find out how we are bringing NF Awareness to people's homes
Read More![](https://nervetumours.org.uk/images/made/images/common/Finalist_artwork370x2801_800_600_s_c1.jpg)
Best Film Nomination “Shine A Light on Neurofibromatosis” PM Society Digital Awards
Join the awards ceremony virtually this Wednesday 16th September
Read More