We’re Here for You, Our NF Community.
09 September 2020
Hello Everyone,
I just wanted to say a very big thank you to absolutely everyone, who has helped us to keep the charity running as usual: by their fundraising efforts; assistance and guidance; and also those who helped to keep up our spirits in the “virtual” head office, over the last six months. Members, supporters, friends, families, the NF medical teams at St Mary’s and Guys & St. Thomas’ and even our local MP! Thank you, to each and every one of you!
We are not sure what the next six months, or even the next year, will bring, but we’re here to take your calls and help where we can. This is a whole new territory for all of us, so please bear with us if things take a little longer, we will all get sorted in the end, but do let me know if there are any major issues, and we will try to help.
We are aiming to move back to the office in the next couple of weeks, a very different looking office as we will all be working behind screens, etc, and apparently you can no longer even share biscuits …….but it will be lovely to be back there with the team!
The shop distribution should return to normal, which is especially important as we will soon launch the sale of our Christmas Cards and other festive items! In the meantime, if anyone has any imaginative and inspiring ideas about how we can raise funds safely in this new, odd world that we live and work in, please do let the team know.
Please do continue to follow the Government guidelines and do take care.
With my very best wishes,
Karen
Filter News
![](https://nervetumours.org.uk/images/made/images/common/jessica-1Page-Preview-800-x-500-px_800_600_s_c1.png)
Jessica’s Amazing Fundraising Efforts
Have a read about the incredible 7 year old fundraising girl who is supporting research into NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/smiling-throughPage-Preview-800-x-500-px_800_600_s_c1.png)
Smiling Through
Have a read about Melanie and her courageous young son Emilio (NF1) and the impact NTUK has had on their lives.
Read More![](https://nervetumours.org.uk/images/made/images/common/mimi-nd-emilioArtboard-1_800_600_s_c1.png)
Our 2019 Christmas Card Competition Winner!
See our Christmas Card winning illustration here
Read More![](https://nervetumours.org.uk/images/made/images/common/Helen-2Page-Preview-800-x-500-px_800_600_s_c1.png)
Helen’s Story
Have a read of loving Mum Helen's Story and how she cares for her wonderful daughter Gaby (NF1)
Read More![](https://nervetumours.org.uk/images/made/images/common/LOOKSPage-Preview-800-x-500-px_800_600_s_c1.png)
Looks and Life: A summary of the study
Have a read about the findings from the UWE's "Looks and Life" Study
Read More![](https://nervetumours.org.uk/images/made/images/common/kate-and-esmePage-Preview-800-x-500-px_800_600_s_c1.png)
Kate’s Story
Have a read of Kate's inspiring story including the introduction of her beautiful daughter Esme, who has NF1, into the world.
Read More![](https://nervetumours.org.uk/images/made/images/common/mel-murrell-2Artboard-1_800_600_s_c1.png)
Insights into the work of our support specialists from Mel Murrell
Meet one of our Support Specialists Mel Murrell and read about her impressions on her first year in the role
Read More![](https://nervetumours.org.uk/images/made/images/common/travelsPage-Preview-800-x-500-px_800_600_s_c1.png)
World At Her Feet
Christina has wrtiten a blog partly about living with NF1 and partly about her travels. Find it here:
Read More![](https://nervetumours.org.uk/images/made/images/common/AroojPage-Preview-800-x-500-px_800_600_s_c1.png)
Arooj: The Fashion Blogger with NF
Arooj Aftab, 22, is an influencer, with NF1, who is known for her baggy fashion style
Read More