Hour of Power – Love Yourself Valentine’s Day workout for NF
15 February 2021
Our NF community came together this Valentine’s Day to get their hearts pumping in support of Laura’s fundraising efforts for the 26,500 affected by Neurofibromatosis in the UK. Nearly 60 people attended the virtual fitness class run by Gavin at Turner Fitness, many “dressing to impress” for the occasion, including Gavin, who did not disappoint!
Laura, whose 3-year-old son Elliot has Neurofibromatosis Type 1 (NF1), has been fundraising for Nerve Tumours UK throughout the month of January. She took on our New Year running challenge aiming to complete 26.5 miles but has now gone on to complete over 80 miles and is still running, aiming to match in miles the total amount she has raised. Running 1 mile for every £ donated. As of now Laura will end up completing a distance approximately the same as from Dover to Dundee – what a champion, she’s really going the extra mile for NF!
![](/images/made/images/common/Laura__Elliot_1200x450_800_300_s_c1.jpg)
If that wasn’t enough already, Laura managed to convince Gavin, Elliot’s uncle to get involved with her fundraising efforts by hosting a one-off Hour of Power on Valentine’s Day. With attendance from all over the UK the zoom fitness class proved to be a big success, raising awareness for those affected by Neurofibromatosis across the country.
Here at Nerve Tumours UK, we want to give a big thank you to Laura & Gavin for all their fundraising efforts, as well as to all those who took part this weekend, spreading the love this Valentine’s Day to our NF community.
Support Laura’s fundraising efforts for Nerve Tumours UK
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Rosalie_Ferner_370x280_800_600_s_c1.jpg)
Neurofibromatosis 1 in the 21st Century
Professor Rosalie Ferner delivers key speech “Neurofibromatosis 1 in the 21st Century” to the BPNA 2022 Annual Conference
Read More![](https://nervetumours.org.uk/images/made/images/common/image_(4)_370x280_800_600_s_c1.jpg)
The International Rare Disease Showcase 1st – 3rd February 2022
The International Showcase is a unique & important event, with interactive sessions taking place from 1st-3rd February 2022
Read More![](https://nervetumours.org.uk/images/made/images/common/Grace_Picture2_370x280_800_600_s_c1.jpg)
Grace’s NF1 story - Nothing stops me
Grace tells us how her NF1 hasn't stopped her from being active and achieving her goals
Read More![](https://nervetumours.org.uk/images/made/images/common/Mia_family_370x280_800_600_s_c1.jpg)
Mia’s NF1 story
Bridie & Warren describe their 17 month old daughter Mia's diagnosis with NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/Ellie_on_rowing_machine_370x280_800_600_s_c1.jpg)
Richard & Diana’s 1,000,000 metre new rowing challenge
Diana & Richard have taken on a 1,000,000 metre rowing challenge in 100 days to raise funds & awareness
Read More![](https://nervetumours.org.uk/images/made/images/common/BZQO9932_370x280_800_600_s_c1.jpg)
A Message from our Charity Director
A message from Karen, our Charity Director, on looking forward to a special 2022
Read More![](https://nervetumours.org.uk/images/made/images/common/Childhood_Neurological_Conditions_Survey_Website_Header_370x280_800_600_s_c1.png)
Childhood Neurological Conditions Survey Part 2
Find out how you can help shape the future of treatment for Childhood Neurological Conditions such as Neurofibromatosis
Read More![](https://nervetumours.org.uk/images/made/images/common/HCTN0411_370x280_800_600_s_c1.jpg)
Graham’s Super Nine Shines A Light on NF
Graham's 7 year old great-nephew Nathan is his inspiration for his epic challenges to fundraise for NTUK
Read More