Westminster Virtual Rare Disease Day 2022 Reception
23 February 2022
Nerve Tumours UK joined the annual international event aimed at raising awareness and highlighting the needs of people with rare diseases.
There are over 6000 rare diseases affecting over 3.5 million people across the UK.
Collectively, rare diseases are not rare.
Today, the rare community came together to raise awareness of the common issues affecting those living with rare conditions.
We joined the Westminster Rare Disease Digital Forum, chaired by Liz Twist, MP and Chair of the APPG on Rare, Genetic and Undiagnosed Conditions, and hosted by the Genetic Alliance.
![](/images/common/image_(3)_1024x768.jpg)
We heard from people affected by rare conditions, discussing the progress of the National Plans for Rare Diseases, which are due to be launched this year.
Maria Caulfield, the Minister responsible for rare conditions, spoke on the future for rare conditions.
![](/images/common/image_(11)_1024x768.jpg)
The Neurofibromatosis community was represented by Dexter Parker who has Neurofibromatosis Type 1, giving insights on how the condition affects his daily life,
![](/images/common/image_(5)_1024x768.jpg)
now a young aspiring student and a story of determination and hope. Thank you Dexter for your support.
![](/images/common/Dexter_1024x768.jpg)
Watch his address to the reception here
Stay tuned on our social channels for Rare Disease Day 2022 on Monday 28th February
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Sarah-Page-Preview-800-x-500-px_800_600_s_c1.png)
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
Read More