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/samantha-gaden_370x280_800_600_s_c1.png)
Statement by Samantha Gaden our Specialist Neurofibromatosis Nurse UK
A statement on coronavirus by Samantha Gaden specialist Neurofibromatosis nurse in the North West
Read More![](https://nervetumours.org.uk/images/made/images/common/melanie-murrell_3_800_600_s_c1.png)
Statement by Melanie Murrell our Specialist Neurofibromatosis Nurse UK
A statement on coronavirus by Melanie Murrell specialist Neurofibromatosis nurse in the West Midlands
Read More![](https://nervetumours.org.uk/images/made/images/common/carolyn-smyth_370x280_800_600_s_c1.png)
Statement by Carolyn Smyth Lead Specialist Neurofibromatosis Nurse UK
A Statement on Coronavirus by Carolyn Smyth Lead Specialist Neurofibromatosis Nurse UK
Read More![](https://nervetumours.org.uk/images/made/images/common/martin-sanchez-Tzoe6VCvQYg-unsplash_370x270_800_600_s_c1.png)
COVID - 19 News from Children’s Tumour Foundation our partners in the US
Covid - 19 News from Children's Tumour Foundation our partners in the US
Read More![](https://nervetumours.org.uk/images/made/images/common/NF_Nurses_370x280_800_600_s_c1.jpg)
Working For The NF Community and Helping to Protect and Save The NHS
Coronavirus is impacting the NHS heavily including our Specialist NF Nurses; help us support them, find out how
Read More![](https://nervetumours.org.uk/images/made/images/common/top-header-rotary-logo-and-name370x280_800_600_s_c1.png)
Leighton Linslade Rotary Club hosts Brains of Leighton Buzzard Quiz
Leighton Linslade Rotary Club hosts Quiz in aid of Neurofibromatosis type 2, find out more here
Read More![](https://nervetumours.org.uk/images/made/images/common/Royal_Society_of_Medicine_-_Medicine_and_Me-370x278px_800_600_s_c1.jpg)
Postponed: Medicine and Me: Living with Nerve Tumours at the Royal Society of Medicine
Postponed: Find out more about the event at the Medicine & Me event at the Royal Society of Medicine here:
Read More![](https://nervetumours.org.uk/images/made/images/common/adolscent-nf1-dayDesktop-1600-x-900-px-copy_800_600_s_c1.png)
NF1 Teenager Support Day!
Bridie Windsor is a Deputy Clinical Nurse Specialist who has organised a support day for teenagers with NF1. Read more here:
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