Dexter’s NF Documentary Project
25 May 2021
Dexter, who has Neurofibromatosis Type 1, is currently studying Film and Media at Ravensbourne University, London. Dexter is the first person in his family with NF, with neither of his parents having it. First diagnosed as a child he spent a lot of time growing up being self-conscious about his NF but has since learned that; we are all different and we should show our differences proudly.
Dexter's documentary project called on members of the NF community to share their daily experiences of living with Neurofibromatosis. Living with the condition himself, he wanted to focus on exactly how people are affected, getting people to open up about the condition so that people can understand the impacts in greater detail and on a more personal level. The documentary is now live and can be viewed below.
The documentary’s theme is ‘Identity & Disability. Diving deep into the truths of disability and the perception of disabilities, as at times disabilities can be generalised as well as misunderstood.
– Dexter"I would also like the focus to steer towards what it really means to have NF, as each person with NF will have a different story. My target audience is teens to young adults with NF, as they may be more self-conscious about who they are as a person. This documentary would hopefully allow them to feel more comfortable in their skin. My target audience will widen to the general public, as especially now during the lockdown, more people are engaging with unknown subjects. This documentary will hopefully be interesting to those viewers who are not only interested in NF but also want to understand and learn more about a different topic, such as Neurofibromatosis."
NTUK supports Dexter in this project as part of our Shine A Light Campaign 2021 "Support the NF Community Make Their Voices Heard in a Changing World"
Please like, comment, and share Dexter’s insightful and honest work with other members of our NF community.
Nerve Tumours UK is not responsible for any data collection or content of the project.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Nurses_Conference_Photo_-_PREVIEW_800_600_s_c1.png)
Nurse’s Conference 2020
Read about how our specialist nurses adapted to covid19 and supported our NF community
Read More![](https://nervetumours.org.uk/images/made/images/common/headway-F2KRf_QfCqw-unsplash370x280_800_600_s_c1.png)
Children’s Tumor Foundation - NF Forum 2020 Moves Online!
Find out how you can take part in CTF's 2020 online NF Forum
Read More![](https://nervetumours.org.uk/images/made/images/common/Pauline__Helen_Article_Website_Header_1600x900_copy_800_600_s_c1.png)
Pauline & Helen Boughen’s PIP Journey
Learn how Helen & her mum Pauline overcame their difficulty with getting the benefits they deserved with Julie Ann Evans help
Read More![](https://nervetumours.org.uk/images/made/images/common/Pipers_School_Rock_Fundraiser_-_370x280_800_600_s_c1.jpg)
Pipers Rocks
Read about Pipers School amazing Rocktastic fundraising efforts for Nerve Tumours UK
Read More![](https://nervetumours.org.uk/images/made/images/common/Mary__Rosalie_370x280_800_600_s_c1.jpg)
Your NF questions answered directly from the Top!!
Get answers to your NF questions directly from our medical advisors
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG-20191225-WA0020_370x280_800_600_s_c1.png)
Planning for a Family - Elena & Nicks Story
Elena describes their journey using Preimplantation Genetic Diagnosis (PGD) to prevent passing on NF1 to their baby.
Read More