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/Hannah_1_370x280_800_600_s_c1.jpg)
Hannah’s NF1 story
9 year old Hannah is running the Junior Great North Run, so other children with NF can also have access to doctors & nurses
Read More![](https://nervetumours.org.uk/images/made/images/common/Sam_Gaden_marathon_2_370x280_800_600_s_c1.jpg)
Sam’s Marathon
Sam, our Specialist NF Nurse for Merseyside & the North West, is running the London Marathon - her very first Marathon!
Read More![](https://nervetumours.org.uk/images/made/images/common/2022_Manchester_370x280_800_600_s_c1.jpg)
NF Patients Community Day
The NF Patients Community Day is on Sunday 9th October 2022 - register to attend virtually
Read More![](https://nervetumours.org.uk/images/made/images/common/Naomi_Marshall_Prof_Heather_Widdows_Susan_Ross__Chrissie_from_CF_370x280_800_600_s_c1.jpg)
Appearance, Identity & Law workshop
Appearance, identity & law workshop at Queen Mary University London School of Law
Read More![](https://nervetumours.org.uk/images/made/images/common/image8_370x280_800_600_s_c1.jpg)
Alfred the Pirate
Seven year old Alfred the Pirate takes NF1 in his stride, and is supported by Specialist NF Nurse Mel
Read More![](https://nervetumours.org.uk/images/made/images/common/Nicole_370x280_800_600_s_c1.jpg)
Nicole’s NF1 story & skydive
Nicole shares her NF1 journey and her motivation to inspire children with disabilities to achieve whatever they want to do
Read More![](https://nervetumours.org.uk/images/made/images/common/photo_collage_370x280_800_600_s_c1.jpg)
Sarah’s NF1 story & Langmead fundraising
Sarah describes her daughter Hannah's NF1 journey and organising a corporate charity day fundraiser at Langmead Herbs
Read More![](https://nervetumours.org.uk/images/made/images/common/Molly__Alfie_370x280_800_600_s_c1.jpg)
Molly & Alfie
Mollie has NF1 - her big brother Alfie & friend Kaelan are running to raise awareness & funds for NTUK
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