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
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2019 NF Conference
Find out more about the 2019 NF Conference being hosted by our friends across the pond the CTF
Read More![](https://nervetumours.org.uk/images/made/images/common/Tipsy-PigPage-Preview-800-x-500-px_800_600_s_c1.png)
Kate Swallow’s Fantastic Fundraiser at the Tipsy Pig
Find out more about the succesful and throughly enjoyed charity music event hosted by Kate Swallow at the Tipsy Pig
Read More![](https://nervetumours.org.uk/images/made/images/common/ruth-drimmerPage-Preview-800-x-500-px_800_600_s_c1.png)
Support Specialist: One of Many Cases
Have a read about a specific case study detailing the kind of work our support specialists offer to those with NF
Read More![](https://nervetumours.org.uk/images/made/images/common/James-Gamble-complete-cover-newDesktop-1600-x-900-px_800_600_s_c1.png)
Thank You James Gamble!
James Gamble just completed an incredible fundraiser in which he has cycled a total of 980 miles for NTUK! Find out more here
Read More![](https://nervetumours.org.uk/images/made/images/common/TeaganPage-Preview-800-x-500-px_800_600_s_c1.png)
Teagan Martin’s first day at Canterbury Secondary School
Have a read about the incredible young girl who continues to defy the odds here
Read More![](https://nervetumours.org.uk/images/made/images/common/KloePage-Preview-800-x-500-px_800_600_s_c1.png)
Kloe van der Merwe - Our NF hero as told by Mum Candice
Hear about the incredibly brave young girl as told by her Mum Candice
Read More![](https://nervetumours.org.uk/images/made/images/common/Wassim-Page-Preview-800-x-500-px_800_600_s_c1.png)
Wass’ Everyday Battlers 10K Stratford Run
Wassim is running the 10K Stratford Run for Nerve Tumours UK. Here he explains his reasons as to why:
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Megan’s Skyfall
Megan is undertaking a sponsored skydive for NTUK as part of her travels! Find out more here
Read More![](https://nervetumours.org.uk/images/made/images/common/Glen-nd-fred-Page-Preview-800-x-500-px_800_600_s_c1.png)
Glen’s Half Marathon in Support of his Nephew Freddie.
Have a read about the special young boy who has inspired his uncle take on the New Forest Half Marathon
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