Stewart Lee Member of the Board of Trustees who has NF2 on Lockdown Life
22 May 2020
I'm Stewart 34 and I am a Member of the Board of Trustees. I have NF2, which I inherited from my dad.
Working in Digital Communications for the past decade in the charity sector and as a Trustee, it has been a joy to see Nerve Tumours digital presence evolve from literally nothing to grow and support so many people. The integration of the community has been great and any voluntary work or fundraising by the community is more than welcome. The team we have in place now launches so many useful campaigns and initiatives to raise awareness about Neurofibromatosis and my social media news feeds are always full of photos of our amazing supporters.
It is important to celebrate World NF 2 day, because we live and endure our lives with such a challenging condition, it's nice to have a day to celebrate how amazing we all are!
![](/images/common/stewart-lee_1024x768.jpg)
Like everyone else it was a shock and such a massive change. Like many others my operation has been postponed (Cochlear Implant) and I was separated from loved ones. My family has adapted well, however zoom calls, homework and social lifes in one small house definitely is a challenge though! I have up and down days, like everyone else, being near to my local parks, captioned zoom meetings and quizzes have really helped! Having the condition is isolating and physically challenging in so many ways, so the extra pressure of the lockdown compounded on that. I feel in a much better place than I did at the start at the lockdown, being able to email my NF nurse for support and to discuss rearranging appointments helped immensely.
Likewise the good weather has helped me chill out when I've needed to!
![](/images/made/images/common/Stewart_2_1024_768_s_c1.jpg)
Small charities like Nerve Tumours UK rely on your unwavering support at critical times like these, our specialist nurses are a credit to the country and without them i dread to think what would happen to families that live with the conditions.
Having steered the charity through the recession in 2008-2011 I know only too well the challenges that charities up and down the country face this year and beyond. I also know of the determination, kindness and resolve that our supporters have to make a difference and that can outshine any challenge that our charity faces, every step walked, penny donated, minute volunteered will make a vital difference to a charity's fortunes.
I like to think having a complex genetic condition has forearmed me with emotional resilience to get through something like this, likewise getting #MentalHealth support and therapy has also been fantastic for dealing with such large lifestyle changes #MentalHealthAwarenessWeek
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Kate_Duncan_370x280_800_600_s_c1.jpg)
Kate’s NF1 Story & DanceAthon
Kate describes her son's NF1 journey and how NTUK supported them
Read More![](https://nervetumours.org.uk/images/made/images/common/all_runners_collage_370x280_800_600_s_c1.jpg)
Strictly Come Running: London Marathon Class of 2021
Congratulations to our class of 2021 London Marathon runners
Read More![](https://nervetumours.org.uk/images/made/images/common/NF2_meeting_2021_collage_370x280_800_600_s_c1.jpg)
Nerve Tumours UK Specialist Neurofibromatosis Nurses attend the 2021 NHS England NF2 meeting
Read more about the England NF2 meeting - working together to improve the experience of NF2 patients
Read More![](https://nervetumours.org.uk/images/made/images/common/DT_2_370x280_800_600_s_c1.jpg)
Douglas Thomson’s NF1 Story
Douglas describes life with NF1 and how losing his leg was one of the best things to happen to him
Read More![](https://nervetumours.org.uk/images/made/images/common/wing_walk_promo2_370x280_800_600_s_c1.jpg)
Tricia’s Wingwalk and Birthday Fundraiser for Sarah and Keith
Tricia's fundraising wingwalk in memory of her daughter Sarah who had NF1, and to remember her father Keith
Read More![](https://nervetumours.org.uk/images/made/images/common/Student_Voice_Prize_logo_370x280_800_600_s_c1.jpg)
Student Voice Prize 2021
The 2021 Student Voice Prize opens on 6th October! #DareToThinkRare for the 8th annual essay competition!
Read More![](https://nervetumours.org.uk/images/made/images/common/CAR_parents_image_1_370x280_800_600_s_c1.jpg)
Centre for Appearance Research - Parent Support Materials Study
The Centre for Appearance Research is doing a study on parent support materials - can you help?
Read More![](https://nervetumours.org.uk/images/made/images/common/YPFI_header_picture_2_370x280_800_600_s_c1.jpg)
Centre for Appearance Research - YP Face IT
YP Face IT offers online support for young people with conditions or injuries affecting their appearance
Read More