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/Mary-nurse-specialistPage-Preview-800-x-500-px_800_600_s_c1.png)
Mary Thomas wins Specialist Nurse of the Year 2019!
Have a read about the Guy's and St Thomas' Celebration of International Nurses Day here
Read More![](https://nervetumours.org.uk/images/made/images/common/Luke-and-his-NF-NinjasPage-Preview-800-x-500-px_800_600_s_c1.png)
Luke and his NF Ninjas
Have a read of Luke's story of growing up with NF and how he plans to bring his chidren up proud of their NF as well.
Read More![](https://nervetumours.org.uk/images/made/images/common/Stannington-park-Page-Preview-800-x-500-px_800_600_s_c1.png)
Stannington Community Association’s Easter Fête
Stannington Community Association's Easter Fête was a success! Read about this years superb event here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Marathon-Page-Preview-800-x-500-px_800_600_s_c1.png)
London Marathon 2019: 26 hard miles for 26,500 people affected
Thank you so much to all our incredible Marathon runners for going the extra mile (or 26)!
Read More![](https://nervetumours.org.uk/images/made/images/common/youtubePage-Preview-800-x-500-px_1_800_600_s_c1.png)
Take a look at our new YouTube Channel
Take a look at our new YouTube channel and how to subscribe here
Read More![](https://nervetumours.org.uk/images/made/images/common/Pear-KellyPage-Preview-800-x-500-px_800_600_s_c1.png)
Meet Pearl
Pearl Kelly is 22, and has multiple complex problems caused by her NF1. Here she explains her outlook on life
Read More![](https://nervetumours.org.uk/images/made/images/common/JoannaPage-Preview-800-x-500-px_800_600_s_c1.png)
Meet Joanna
Joanna is a lecturer in Mitochondrial Genetics at Newcastle University, she recently ran the London Marathon. Meet her here
Read More![](https://nervetumours.org.uk/images/made/images/common/Maia-Thornton-ResearchPage-Preview-800-x-500-px_800_600_s_c1.png)
New Research Into Appearance Altering Conditions
Maia Thornton PhD is looking for both parents and professionals who care for someone with an appearence altering condition
Read More![](https://nervetumours.org.uk/images/made/images/common/AdamPage-Preview-800-x-500-px_800_600_s_c1.png)
Adam’s Story
Adam has NF1 yet is still one of the most active and athletic people in the UK. Read about his fascinating story here:
Read More