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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Benefit and Financial Support Matters answered by our Specialist
Find out how you can get your disability benefits and financial support questions answered
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Nerve Tumours UK Specialist Neurofibromatosis Nurses attend the 2020 NHS England NF2 Meeting
Find out what went on at the NF2 National Conference and how patient feedback has played a crucial role in improving services
Read More![](https://nervetumours.org.uk/images/made/images/common/Megan_370x280_preview_800_600_s_c1.jpg)
Meeting Megan
Read about how Megan channels her NF1 challenges and uses it as a drive for positive change!
Read More![](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
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