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.
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Neurofibromatosis 1 in the 21st Century
Professor Rosalie Ferner delivers key speech “Neurofibromatosis 1 in the 21st Century” to the BPNA 2022 Annual Conference
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The International Rare Disease Showcase 1st – 3rd February 2022
The International Showcase is a unique & important event, with interactive sessions taking place from 1st-3rd February 2022
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Grace’s NF1 story - Nothing stops me
Grace tells us how her NF1 hasn't stopped her from being active and achieving her goals
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Mia’s NF1 story
Bridie & Warren describe their 17 month old daughter Mia's diagnosis with NF1
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Richard & Diana’s 1,000,000 metre new rowing challenge
Diana & Richard have taken on a 1,000,000 metre rowing challenge in 100 days to raise funds & awareness
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A Message from our Charity Director
A message from Karen, our Charity Director, on looking forward to a special 2022
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Childhood Neurological Conditions Survey Part 2
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/HCTN0411_370x280_800_600_s_c1.jpg)
Graham’s Super Nine Shines A Light on NF
Graham's 7 year old great-nephew Nathan is his inspiration for his epic challenges to fundraise for NTUK
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