Rarefest 2020
20 November 2020
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The festival covers Neurofibromatosis and has various speakers from the NF community as part of its program.
In true 2020 style, RAREfest20 promises to be a virtual feast that will spark curiosity, challenge perceptions, inspire innovation and collaboration and give a voice to rare disease patients and their families.
RAREfest20 has patients at its heart with science and technology running through its veins! The full live programme is ready to view in the agenda tab above. For a peek of what you can expect, head to our highlights, speakers and exhibitors’ pages brimming with cool companies, scientists, tech experts, health pros and patients taking part.
Open to the general public, patients, families, children, students, healthcare professionals, researchers, companies. To everyone!
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![](https://nervetumours.org.uk/images/made/images/common/image0_(1)_800_600_s_c1.jpeg)
Andrea’s Story
Andrea shares her long journey for an NF diagnosis and why she wants her story out there.
Read More![](https://nervetumours.org.uk/images/made/images/common/Caroline_Advice_Newsletter_(6)_800_600_s_c1.png)
Advice for Students with NF1, NF2-Schwannomatosis, and Schwannomotosis
Expert advice, information and resources to help you get the most from university.
Read More![](https://nervetumours.org.uk/images/made/images/common/Ella_Image_(2)_800_600_s_c1.jpg)
Ella’s Story
Ella shares her insights into campus life with NF, her victories and hurdles and the importance of self belief.
Read More![](https://nervetumours.org.uk/images/made/images/common/image7_(1)_800_600_s_c1.jpeg)
Georgia’s Story
Georgia shares her her story of self celebration, the importance of difference and how perseverance is key.
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_8285_(1)_800_600_s_c1.jpg)
Nottingham INFormation Day a Big Thank You
Photos, feedback and more from the Nerve Tumours UK INFormation day in Nottingham.
Read More![](https://nervetumours.org.uk/images/made/images/common/Quality_of_Life_Surveywebnews_800_600_s_c1.png)
Quality of Life Survey
If you're living with NF, or a part of someone's network of support; we need your feedback.
Read More![](https://nervetumours.org.uk/images/made/images/common/Website_Header_800_600_s_c1.png)
Advice: Travelling With NF
Learn how to navigate travel with NF confidently. Essential tips and resources for smooth, stress-free journeys by train, pla
Read More![](https://nervetumours.org.uk/images/made/images/common/NF1CNC_Post124312_800_600_s_c1.png)
Join the NF1 Cutaneous Neurofibroma Consortium Project
Join a groundbreaking NF1 study to help develop better treatments for neurofibromas. Open to adults with a clinical/genetic N
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