“Happy Easter”
14 April 2022
“Happy Easter”
I hope you are all enjoying the long bank holiday weekend!
Easter is quite late this year, and we will soon enter May – World Neurofibromatosis Awareness Month, an even more special time for us this year, as we celebrate forty years of the charity being in existence. The charity has faced many storms over the years, not least over the last two years, when Covid forced the world into lockdown. Although we carried on with business as usual as best we could, our finances took a beating.
Therefore, I would really like to thank our supporters, who are now starting to get out and about, raising both awareness and funds. Quite simply, without you, we would not be able to deliver our services. We hope to meet up with many of you over the coming months, be it at the London Cycle Event, the various marathons, or at the Neurofibromatosis Conference to be held in Manchester in October.
Regarding the conference, we recently helped by distributing a survey asking what was of interest and what was most important for our community to hear and learn about, and I was delighted to see that the message to both the key players in the NF community, and to the charity, has not changed from the survey we ran two years ago.
Access to support services are still key, and with this you have the complete and unwavering backing of the charity. With a hopeful return to pre Covid fundraising, we will be focusing our attention on parts of the country deprived of regional support. Everyone should have the same level of access to support. To assist with the expansion of our Specialist Neurofibromatosis Network, we need to continue raising awareness of what we do. To that end, Nerve Tumours UK have joined forces with RBH Creative Communications, to launch a nationwide awareness campaign, to engage with the wider British public.
As ever, it is so important that you have your say, so please do participate in all surveys or research questionnaires that we distribute, or talk to us directly. You will be helping to make yours and everyone else’s daily life just that bit better.
Here's to our fortieth year of raising awareness.
With my very best wishes,
Karen
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Workplace_resources_preview_370x280_800_600_s_c1.jpg)
Equality, Diversity and Inclusion in the Workplace
Nerve Tumours are here to support you in the workplace: iNForm; workplace equality research & creating an inclusive workplace
Read More![](https://nervetumours.org.uk/images/made/images/common/Wayne_Littlewood_2_370x280_800_600_s_c1.jpg)
Wayne’s World of Marathons
Read about Wayne's world: marathons, running a wedding fayre business with wife Leanne and their son Harley who has NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/London_Marathon_2023_preview_370x280_800_600_s_c1.jpg)
Team NTUK London Marathon 2023
Meet some of our runners and read their inspiring marathon motivation stories
Read More![](https://nervetumours.org.uk/images/made/images/common/Pip_Vilday_running_vest_370x280_800_600_s_c1.jpg)
Pip’s London Marathon
Pip describes life with NF1 & limited vision and his motivation to run the London Marathon
Read More![](https://nervetumours.org.uk/images/made/images/common/image_(48)_370x280_800_600_s_c1.jpg)
The Scottish Parliament Rare Disease Day Online Reception 15/03/2023
NTUK attended the Scottish Parliament Rare Disease Day online reception
Read More![](https://nervetumours.org.uk/images/made/images/common/Screenshot_2023-03-03_at_11.20.57_370x280_800_600_s_c1.jpg)
Support Derry’s and Dan’s Marathon Run for NTUK
Dan and Derry will be taking on the London Marathon in support of Nerve Tumours UK
Read More![](https://nervetumours.org.uk/images/made/images/common/0BCDA8DF-DF60-47D5-A705-BB6EE3A5BBEF_370x280_800_600_s_c1.jpg)
Ragbir’s London Marathon
Ragbir is the Paediatric Lead for NF1 in Leeds and is running the London Marathon
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_8289_370x280_800_600_s_c1.jpg)
Rare Disease Day 2023
NTUK joined in with Rare Disease Day 2023, helping raise awareness of how better coordination of care can improve lives.
Read More