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!
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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!
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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/durham-researchPage-Preview-800-x-500-px_800_600_s_c1.png)
New research into non-discrimination law
Durham University is looking for participants who look different due to their health complications. such as NF.
Read More![](https://nervetumours.org.uk/images/made/images/common/MichaelFry2_800_600_s_c1.png)
Letter from our new Chair
A letter detailing the vision of our new chair, and the future of the charity.
Read More![](https://nervetumours.org.uk/images/made/images/common/NTUK-logo_800x500px_800_600_s_c1.gif)
Launch of Nerve Tumours UK
Following a major strategic review, the Neuro Foundation charity is now known as Nerve Tumours UK.
Read More![](https://nervetumours.org.uk/images/made/images/common/shruti-garg_800_600_s_c1.jpg)
NF1 research award first for UK consultant
Dr Shruti Garg is the first non-US resident to receive NF1 $555,000 research award.
Read More![](https://nervetumours.org.uk/images/made/images/common/PoppyPage-Preview-800-x-500-px_800_600_s_c1.png)
Polly’s Story (as told by Mum Emily)
"Despite being on weekly chemotherapy she is a happy child and never fails to inspire us all"
Read More![](https://nervetumours.org.uk/images/made/images/common/eden-baby_800_600_s_c1.jpg)
EDEN Study Progress Report
The EDEN study has enrolled 30 babies and toddlers to understand how infants with NF1 develop.
Read More![](https://nervetumours.org.uk/images/made/images/common/EllaPage-Preview-800-x-500-px_800_600_s_c1.png)
Ella’s story
Have a read of Ella's story here. An uphill battle which we know she will turn around!
Read More![](https://nervetumours.org.uk/images/made/images/common/Grace-colourPage-Preview-800-x-500-px_800_600_s_c1.png)
Grace’s Story
Have a read of Grace's story and she overcame her insecurites surrounding her NF
Read More![](https://nervetumours.org.uk/images/made/images/common/Helpful_Charities_800x500_preview_800_600_s_c1.jpg)
Helpful Charities
Find some of the other helpful charities that may be able to support you here
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