World NF2 Day 2021 Emily Owen Member of our Board of Trustees Takes over our social
20 May 2021
Happy NF2 Day 2021
My name's Emily. I am a Trustee of Nerve Tumours UK and I have NF2 so, when I say 'Happy NF2 Day,' I'm not thinking that everything about NF2 is happy! I know it's not! but I do know that on NF2 Day we can unite, we can join together and we can celebrate each other and make sure that the voices of those affected with Neurofibromatosis Type 2 are heard in a changing world.
So, throughout today, at 22 minutes past the hour - 22 because NF2 is a gene defect on chromosome 22 so, 22 minutes past the hour there will be a post on NTUK's social media channels.
It will just be a little HAIKU poem, which it would be great if you comment on, or like, or share, so we can all join together and be a real NF2 family today.
So, yes, Happy NF2 Day, everyone!
![](/images/common/Artboard_1_1.jpg)
![](/images/common/Artboard_1_copy.jpg)
![](/images/common/Artboard_1_copy_2.jpg)
![](/images/common/Artboard_1_copy_3.jpg)
![](/images/common/Artboard_1_copy_4.jpg)
![](/images/common/Artboard_1_copy_5.jpg)
![](/images/common/Artboard_1_copy_6.jpg)
![](/images/common/Artboard_1_copy_7.jpg)
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Changing_Faces_Logo_370x280_800_600_s_c1.jpg)
Counselling support from Changing Faces
Changing Faces - Counselling support: confidential one to one support sessions for people with a visible difference
Read More![Nerve Tumours UK Community Survey](https://nervetumours.org.uk/images/made/images/templates/placeholder_800_600_s_c1.png)
Nerve Tumours UK Community Survey
This consultation provided direct feedback to the strategy group, to look at how we can continue to provide our services
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_7819_-_Suzi_NF2_-_edit_370x280_800_600_s_c1.jpg)
Suzi’s NF2 story
Suzi used her own NF2 diagnosis to inspire her research into how identity is experienced by people with NF2
Read More![](https://nervetumours.org.uk/images/made/images/common/Emma_Hartley_Liverpool_Fundraiser_Image_5_370x280_800_600_s_c1.jpg)
Emma’s Story
Emma shares her journey with NF after finding out her daughter, Poppy, has been diagnosed with NF Type 1.
Read More![](https://nervetumours.org.uk/images/made/images/common/tegan-mierle-fDostElVhN8-unsplash_preview_800_600_s_c1.jpg)
Tim’s Story: Living With Neurofibromatosis – it’s a family thing
Tim tells us how Nerve Tumours UK proved to be an invaluable resource and support to him and his family as he was growing up
Read More![](https://nervetumours.org.uk/images/made/images/common/Out_Walking_370x280_800_600_s_c1.jpg)
Dalvinder’s 100km Ultra Challenge for NF
Dalvinder on the 100km Ultra Challenge Thames Path walk to raise money for NF
Read More![](https://nervetumours.org.uk/images/made/images/common/Diana_Edwards_Nerve_Tumours_UK_Fundraiser_image_5_800_600_s_c1.png)
Diana’s One Month of Rowing for Neurofibromatosis
Diana is taking on an epic 150k rowing challenge - 5k per day to support her daughter Ellie & our NF community
Read More![](https://nervetumours.org.uk/images/made/images/common/Autistica_Research_Festival_Branded_Header_preview_800_600_s_c1.png)
Autistica Research Festival 2021
See how this year's event went and find out how you can watch the best bits if you couldn't make the conference.
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_1837_Carol_Irving_Nurse_Portrait_preview_800_600_s_c1.jpg)
OneMoreNurse joins the NTUK team in Leeds
We're delighted to announce our new Specialist NF Nurse for Leeds, find out more
Read More