Rare Disease Day 2021 and Rare Reach Festival
15 February 2021
Rare Disease Day 2021 will take place on Sunday 28 February
Nerve Tumours UK takes part as a member of the Genetic Alliance. This is a chance to raise awareness amongst the general public and decision-makers about rare conditions and their impact on people’s lives. This year, in light of Covid-19, it will be harder than ever to ensure the voices of the UK’s rare community are heard.
We invite you to join in - you can share your story on social media until 12.03.2021- using the hashtag #RareReach2021 alongside the #RareDiseaseDay2021 hashtag, and if appropriate, one of the Rare Disease Day themes – #RareIsStrong, #RareIsMany, #RareIsProud.
Rare Reach Festival
Showcasing digital storytelling
STORYTELLING IS POWERFUL. As part of Rare Disease Day 2021, the Genetic Alliance is launching the first Rare Reach Festival to celebrate the online storytelling by the genetic, rare and undiagnosed community.
By posting real-life stories (funny, sad, inspirational and everything in between) on social media, people affected by rare conditions share their day-to-day experiences to help raise awareness of how their lives are impacted by their condition. These stories also help reach out to others in the same situation offering solidarity, hope and community.
Nerve Tumours UK wants to celebrate and encourage this storytelling. We are inviting everyone in the Nerve Tumours community to tell their story in a social post or repost any old posts that give you a voice, anything that is part of your condition, a fundraiser you have done for us or a story that you support. Rare is strong; Rare is many; Rare is proud.
You can join the Rare Reach official competition until 12.03.2021
Filter News
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Jonny’s Story
Jonny has chosen to open up and share his incredibly brave battle with Cancer over the past year, find out more here:
Read More![](https://nervetumours.org.uk/images/made/images/common/james_2__800_600_s_c1.jpg)
James on Tour
James Wiggin is taking on the Tour de France on behalf of Nerve Tumours UK – or at least a part of it.
Read MoreNerve Tumours UK Specialist Neurofibromatosis Nurses attend the National NF1 Meeting in Manchester
Have a read what was talked about at this year's National NF1 Meeting in Manchester
Read More![](https://nervetumours.org.uk/images/made/images/common/lets-go-regional-coverPage-Preview-800-x-500-px_800_600_s_c1.png)
Let’s Go Regional/ Let’s Go Outside
Read about the website that offers new exciting opportunities to help you find a fundraiser/event that is most suited to you
Read More![](https://nervetumours.org.uk/images/made/images/common/Meet-harley-Mobile-600-x-800-px_800_600_s_c1.png)
Meet Harley
Have a read about the amazing 7 year old boy with NF1 and his fundraising family
Read More![](https://nervetumours.org.uk/images/made/images/common/PerculiarArtboard-1_800_600_s_c1.png)
Funny Peculiar
Peculiar Productions has chosen to donate all their proceedings to NTUK this year! Find out more:
Read More![](https://nervetumours.org.uk/images/made/images/common/christmas-card-website-2019Page-Preview-800-x-500-px_800_600_s_c1.png)
Christmas Card Competition 2019
Check out this year's Christmas Card Competition and how to enter
Read More![](https://nervetumours.org.uk/images/made/images/common/LanyardsPage-Preview-800-x-500-px_800_600_s_c1.png)
Sunflower lanyards to support patients and visitors with hidden disabilities
Read about the new lanyards being given out at Heathrow, Sainsbury's and Gatwick to help support those with disabilities
Read More![](https://nervetumours.org.uk/images/made/images/common/Small-Charity-NTUKPage-Preview-800-x-500-px_800_600_s_c1.png)
NTUK attends Small Charity Week
Nerve Tumours UK attended Small Charity Week, find out more about the week and why we attended here:
Read More