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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Jessica’s Amazing Fundraising Efforts
Have a read about the incredible 7 year old fundraising girl who is supporting research into NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/smiling-throughPage-Preview-800-x-500-px_800_600_s_c1.png)
Smiling Through
Have a read about Melanie and her courageous young son Emilio (NF1) and the impact NTUK has had on their lives.
Read More![](https://nervetumours.org.uk/images/made/images/common/mimi-nd-emilioArtboard-1_800_600_s_c1.png)
Our 2019 Christmas Card Competition Winner!
See our Christmas Card winning illustration here
Read More![](https://nervetumours.org.uk/images/made/images/common/Helen-2Page-Preview-800-x-500-px_800_600_s_c1.png)
Helen’s Story
Have a read of loving Mum Helen's Story and how she cares for her wonderful daughter Gaby (NF1)
Read More![](https://nervetumours.org.uk/images/made/images/common/LOOKSPage-Preview-800-x-500-px_800_600_s_c1.png)
Looks and Life: A summary of the study
Have a read about the findings from the UWE's "Looks and Life" Study
Read More![](https://nervetumours.org.uk/images/made/images/common/kate-and-esmePage-Preview-800-x-500-px_800_600_s_c1.png)
Kate’s Story
Have a read of Kate's inspiring story including the introduction of her beautiful daughter Esme, who has NF1, into the world.
Read More![](https://nervetumours.org.uk/images/made/images/common/mel-murrell-2Artboard-1_800_600_s_c1.png)
Insights into the work of our support specialists from Mel Murrell
Meet one of our Support Specialists Mel Murrell and read about her impressions on her first year in the role
Read More![](https://nervetumours.org.uk/images/made/images/common/travelsPage-Preview-800-x-500-px_800_600_s_c1.png)
World At Her Feet
Christina has wrtiten a blog partly about living with NF1 and partly about her travels. Find it here:
Read More![](https://nervetumours.org.uk/images/made/images/common/AroojPage-Preview-800-x-500-px_800_600_s_c1.png)
Arooj: The Fashion Blogger with NF
Arooj Aftab, 22, is an influencer, with NF1, who is known for her baggy fashion style
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