RARE Champion of Hope Celebration
20 October 2020
Groundbreakers. Leaders. Advocates.
The rare disease community is full of people who inspire us all through innovation, research, compassion and a relentless spirit to affect positive change. Through the RARE Champion of Hope Awards, we honor and recognize true champions for rare disease. This year we will be recognizing leaders who have made a significant impact in advocacy, industry, medical care, science, as well as up-and-coming rare disease leaders. Awardees will be announced at this year’s RARE Champion of Hope Celebration.
Register for your place at the RARE Champion of Hope Celebration, taking place 12th November 2020, 7pm-8pm. RSVP today for a virtual gala; experience exciting food and drink demos, entertaining performances, and inspiring stories of hope from the rare disease community.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Night_time_runs-_preview_800_600_s_c1.jpg)
24 Hour Marathon – Three Brothers Running for the Fourth
Toby, James & Alex take on an epic 24 hour marathon race to commemorate their brother Tristan
Read More![](https://nervetumours.org.uk/images/made/images/common/Parent_support_research_advert_370x280.png_800_600_s_c1.jpg)
Centre for Appearance Research NF Survey - Results
Find out how you can take part in CAR's online survey about NF parenting and caring experiences.
Read More![](https://nervetumours.org.uk/images/made/images/common/EC_COVID-19_survey_1_preview_800_600_s_c1.jpg)
Share your Covid-19 Story - Survey Results
Embracing Complexity share the results of their impact of Covid19 survey, find out more
Read More![](https://nervetumours.org.uk/images/made/images/common/Hour_of_Power_Fitness_Class__Gavin_370x280_800_600_s_c1.jpg)
Hour of Power – Love Yourself Valentine’s Day workout for NF
Thanks to all those that got their hearts pumping this Valentine's Day for our NF community!
Read More![](https://nervetumours.org.uk/images/made/images/common/Rare_Disease_Festival_Website_preview_370x280_800_600_s_c1.jpg)
Rare Disease Day 2021 and Rare Reach Festival
Find out how you can get involved in the first ever Rare Reach Festival and make sure the Rare communities voice is heard!
Read More![](https://nervetumours.org.uk/images/made/images/common/preview_800_600_s_c1.png)
NF Said
Daisy takes on a 38-mile running challenge for her sister Millie, 1 mile a day for every person diagnosed with NF2 a year
Read More![](https://nervetumours.org.uk/images/made/images/common/1_800_600_s_c1.png)
Love Yourself - Hour of Power in Support of the NF community
Get your sweat on and spread the love this Valentine's day for our NF community!
Read More![](https://nervetumours.org.uk/images/made/images/common/Patrick_Walk_Day_1_image_2_370x280_800_600_s_c1.png)
Pat’s NF Fundraiser Walk
Read all about Patrick's incredible fundraising efforts to help others affected by NF!
Read More