Shine A Light on Neurofibromatosis now streaming on The Disorder Channel
09 September 2020
With Its Film Fest Postponed by the Pandemic, Rare Outreach Coalition starts its own Streaming Channel "The Disorder Channel” and Nerve Tumours UK is part of it with its movie Shine A Light on Neurofibromatosis to raise awareness for those affected by the condition.
The goal of Rare Outreach Coalition is to create opportunities for education, awareness, conversations, and collaborations across multiple rare disease communities.
Rare Outreach Coalition was forced to postpone its May 18th event in New York City (Disorder: The Rare Disease Film Festival) due to COVID-19. ROC has now launched The Disorder Channel as a new platform to provide another showcase for rare disease films. It features many previously unseen rare films and original videos. The channel also includes some films intended for this year’s festival, as well as favourites from previous years. The aim is to raise awareness, find a cure and spread hope for those affected with a rare disease or a genetic disorder.
Our movie does have a global reach and attracts not only viewers that are affected but predominantly attracts those working in the medical profession. The stories of Emily Owen and the Burbridge Family support the founders and our cause to raise awareness and will educate those who are not aware of the impact to a persons live affected by the condition. Nerve Tumours UK is more than grateful to be able to be part of the platform from its beginning.
![](/images/made/images/common/disorder_channel_1200x450_800_300_s_c1.jpg)
The Disorder Channel is now available to the millions of homes with a Roku or Amazon Fire TV. Just search for The Disorder Channel to add it to your device. You can also add the channel to your Roku device with our code DISORDERTV. We’ve collected films about the rare disease patient experience. Stories of hope in the face of the longest odds.
This year the Disorder Channel is one of the Partners at the Global Genes A RARE Patient Advocacy (un)Summit, you can find more details and register for the summit below.
Read about how our Shine A Light Movie made finalist at the PM Society Awards 2020
Read More![](/images/common/PM_Society_Awards_Certificate_1024x768.png)
Filter News
![](https://nervetumours.org.uk/images/made/images/common/The_Faces_of_NF_At_Xmas_3.70X280_800_600_s_c1.jpg)
2020 A Review
2020 was hard for everyone but our NF community is stronger & more resilient than ever. Read our reflections on 2020
Read More![](https://nervetumours.org.uk/images/made/images/common/Genna_NF_Story_370x280_800_600_s_c1.jpg)
Geena’s Story
James Harkness talks about his late mother Geena Andrews & what Nerve Tumours UK meant to her.
Read More![](https://nervetumours.org.uk/images/made/images/common/Xmas-Party-Heroes-Web-5_Donation370x280_800_600_s_c1.jpg)
Xmas Party Superheroes
Had your Xmas party cancelled? Find out how you can save the day & become instant #XmasPartyHeroes
Read More![](https://nervetumours.org.uk/images/made/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_370x280_800_600_s_c1.jpg)
Lee’s Santa Dash
Check out Lee's Festive Santa Dash for NF and see how you can get involved
Read More![](https://nervetumours.org.uk/images/made/images/common/Karen__NF_Community_370x280_800_600_s_c1.jpg)
Thinking Forward to 2021 - A Message from our Charity Director
A message from Karen our Charity Director on looking forward to the year ahead
Read More![](https://nervetumours.org.uk/images/made/images/common/RAREfest20-eventbrite-email-image-2_370x280_800_600_s_c1.jpg)
Rarefest 2020
RAREfest20: a free virtual, interactive science, technology, advocacy & arts exhibition with a rare twist. Visit exhibition
Read More![](https://nervetumours.org.uk/images/made/images/common/derek_370x280_800_600_s_c1.jpg)
Kebabathon for Nerve Tumours UK
Find out why Des is taking on this Mammoth Meat Mission for Nerve Tumours UK
Read More