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
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Sarah’s Story
Sarah has NF1 and works full time for the NHS check out her intriguing story here
Read More![](https://nervetumours.org.uk/images/made/images/common/laura-2Desktop-1600-x-900-px-copy_800_600_s_c1.png)
Laura’s Story
Read about Laura's experience of undergoing surgery to remove a tumour from her spine here:
Read More![](https://nervetumours.org.uk/images/made/images/common/durhamPage-Preview-800-x-500-px_800_600_s_c1.png)
Visible Difference Equality Law Research: summary of findings
Find out more about the results here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Galloway-Page-Preview-800-x-500-px_800_600_s_c1.png)
The Galloway Family and their “amazing” four year old Ruby
Have a read about the incredibly brave young Ruby Galloway (NF1) and check out their previous and future fundraiers.
Read More![](https://nervetumours.org.uk/images/made/images/common/James-blog-3Page-Preview-800-x-500-px_800_600_s_c1.png)
“Framing the face: History, Emotion, Transplantation” a blog from James Partridge
Find out more about the blog and what is concerns here:
Read More![](https://nervetumours.org.uk/images/made/images/common/halloween-Page-Preview-800-x-500-px_800_600_s_c1.png)
A Spooktacular Halloween day for NTUK
Find out more about the wonderful fundraising event here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Nick-and-elidihDesktop-1600-x-900-px-copy_800_600_s_c1.png)
Nicks Triathlon in Support of his daughter Eilidh
Find out more about Nick's Triathlon and his daughter's experiences with NF1 here:
Read More![](https://nervetumours.org.uk/images/made/images/common/TOM-GK-MusicalPage-Preview-800-x-500-px_800_600_s_c1.png)
Tom GK- Hearing Loss: The Musical
Find out more about the musical and how you can secure your ticket here
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