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.
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Tate’s Shine A Light Marathons
Support Tate with his 2023 Shine A Light 100 mile Challenge
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_20230214_094714_370x280_800_600_s_c1.jpg)
Beth’s NF1 story
"I had no idea what NF was until I got diagnosed with it." Beth shares her NF1 journey to help raise awareness
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Shine A Light 2023
The Shine A Light 2023 campaign had 162 buildings around the UK & the Republic of Ireland lit up in blue!
Read More![](https://nervetumours.org.uk/images/made/images/common/Christine_Grant__Margaret__Sheila__Maureen_370x280_800_600_s_c1.jpg)
Christine’s Coronation fundraising
Christine has been fundraising for NTUK for 10 years, since her grandson was diagnosed with NF1.
Read More![](https://nervetumours.org.uk/images/made/images/common/PXL_20220930_101710232_370x280_800_600_s_c1.jpg)
Megan’s NF1 story
Megan has NF1 & other complications: "I will always live my life to the fullest and not let my diagnosis stand in my way"
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Shine a Light May 2023
Shine A Light Activities during World NF Month May 2023 - Get Involved!
Read More![](https://nervetumours.org.uk/images/made/images/common/image1_(11)_370x280_800_600_s_c1.jpg)
Charlotte’s NF1 story
Charlotte and her brother & dad have NF1. She is running the Shine a Light Marathon during May to raise awareness
Read More![](https://nervetumours.org.uk/images/made/images/common/Screenshot_2023-05-10_174650_370x280_800_600_s_c1.jpg)
Be seen, be counted: #PicsForThe1in6
Be part of the Neurological Alliance's photo collage, representing people with neurological conditions
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