The results are in for our Nerve Tumours UK film nominated at the Rare diseases film festival!
05 March 2020
![](/images/made/images/common/rare_film_festival_banner_jpg_800_323_s.jpg)
Voting for the Peoples Choice Award at the Rare Film Festival 2020 has now closed and the results are in!
Unfortunately Nerve Tumours UK did not win but we are proud to have been selected and given the opportunity to spread the message for neurofibromatosis & schwannomatosis in the UK. We would like to say a huge thank you to the 260 people who voted for our film "Shine A Light on Neurofibromatosis"!
Congratulations to all of the participants and for anyone who hasn't seen our film yet you can check it out on our YouTube channel below.
Nerve Tumours UK film shortlisted at first ever rare diseases film festival!
Rare Disease UK as part of the Genetic Alliance is hosting the UK’s first ever film festival that is dedicated to raising awareness of rare diseases.
Our entry "Shine A Light on Neurofibromatosis" has been shortlisted as potential winner of 'Best Charity Film' category. The festival had over 50 entries. The Awards Ceremony will take place on the 10th of February at Regent Street Cinema, at 6:30 pm.
During the night the winner of all the categories will be announced.
Nerve Tumours UK took part in the festival in order to raise awareness for those that are affected by Neurofibromatosis Type 1 and Type 2 and reach a wider audience. Please have a look at the video below. We are more than grateful to the Burbdrige family and Emily Owen for sharing their stories on camera. Feel free to share.
![](/images/made/images/common/Film-festival-2Page-Preview-800-x-500-px_800_600_s_c1.png)
![](/images/made/images/common/Film-festival-2Page-Preview-800-x-500-px-copy_800_600_s_c1.png)
– Phil K Matthew Film Director"Making this film and raising awareness of NF Type 1 and NF Type 2 - specifically capturing the stories of those that are affected - was incredibly fascinating. Films should always have a strong narrative and being able to share their inspiring stories and their courageous journey through adversity, was both heart-warming and inspirational. "
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Night_time_runs-_preview_800_600_s_c1.jpg)
24 Hour Marathon – Three Brothers Running for the Fourth
Toby, James & Alex take on an epic 24 hour marathon race to commemorate their brother Tristan
Read More![](https://nervetumours.org.uk/images/made/images/common/Parent_support_research_advert_370x280.png_800_600_s_c1.jpg)
Centre for Appearance Research NF Survey - Results
Find out how you can take part in CAR's online survey about NF parenting and caring experiences.
Read More![](https://nervetumours.org.uk/images/made/images/common/EC_COVID-19_survey_1_preview_800_600_s_c1.jpg)
Share your Covid-19 Story - Survey Results
Embracing Complexity share the results of their impact of Covid19 survey, find out more
Read More![](https://nervetumours.org.uk/images/made/images/common/Hour_of_Power_Fitness_Class__Gavin_370x280_800_600_s_c1.jpg)
Hour of Power – Love Yourself Valentine’s Day workout for NF
Thanks to all those that got their hearts pumping this Valentine's Day for our NF community!
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 and Rare Reach Festival
Find out how you can get involved in the first ever Rare Reach Festival and make sure the Rare communities voice is heard!
Read More![](https://nervetumours.org.uk/images/made/images/common/preview_800_600_s_c1.png)
NF Said
Daisy takes on a 38-mile running challenge for her sister Millie, 1 mile a day for every person diagnosed with NF2 a year
Read More![](https://nervetumours.org.uk/images/made/images/common/1_800_600_s_c1.png)
Love Yourself - Hour of Power in Support of the NF community
Get your sweat on and spread the love this Valentine's day for our NF community!
Read More![](https://nervetumours.org.uk/images/made/images/common/Patrick_Walk_Day_1_image_2_370x280_800_600_s_c1.png)
Pat’s NF Fundraiser Walk
Read all about Patrick's incredible fundraising efforts to help others affected by NF!
Read More