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/Littlewoods-charityPage-Preview-800-x-500-px_800_600_s_c1.png)
Littlewood’s Charity Night
Have a read of yet another successful charity night hosted by the Littlewoods
Read More![](https://nervetumours.org.uk/images/made/images/common/Emily-owenPage-Preview-800-x-500-px_800_600_s_c1.png)
Emily Owen Positive Role Model (Disability) Award Nomination
Vote for our tustee Emily Owen at this year's National Diversity Awards 2019.
Read More![](https://nervetumours.org.uk/images/made/images/common/gareth-evans-Page-Preview-800-x-500-px_800_600_s_c1.png)
Research Outlook with Prof Gareth Evans
Have a read on some of the latest research with Prof Gareth Evans
Read More![](https://nervetumours.org.uk/images/made/images/common/Ben-fundraiser-dinnerPage-Preview-800-x-500-px_800_600_s_c1.png)
ICAEW Worcestershire Annual Dinner and Ball Fundraiser for NTUK
The ICAEW Worcestershire Annual Dinner and Ball raised an incredible amount for us this year! Find out more here:
Read More![](https://nervetumours.org.uk/images/made/images/common/White-family-coverPage-Preview-800-x-500-px_800_600_s_c1.png)
We are Family London Marathon
Have a read of the remarkable journey the White family has undergone in support of their young daughter Gaby who has NF.
Read More![](https://nervetumours.org.uk/images/made/images/common/Shine-a-Light_1600x900px_800_600_s_c1.jpg)
Shine a Light on Neurofibromatosis
World Neurofibromatosis Awareness Day - May 17th. Help us raise £ 26,500 for 26,500 people in the UK who have nerve tumours.
Read More![](https://nervetumours.org.uk/images/made/images/common/jem-nd-richPage-Preview-800-x-500-px_800_600_s_c1.png)
Jem Musselwhite and Rich White are fundraising by walking the Pilgrims’ Way
Jem and Rich are walking more than 100 miles to raise money for Nerve Tumours UK. Find out more here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Rachel-Page-Preview-800-x-500-px_800_600_s_c1.png)
Meet Rachael
Rachael Reynolds is a 43-year-old mother of four, living in Huddersfield. She recently appeared in the Channel 5 programme,
Read More![](https://nervetumours.org.uk/images/made/images/common/Beijing-MarathonPage-Preview-800-x-500-px_800_600_s_c1.png)
Meet Our Two Marathon Runners from China
Meet our two runners from China who like to partake in marathons across the globe.
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