NF1 Army’s incredible 10 million steps fundraiser!
02 July 2020
Our most recent fundraiser has been completed in lockdown. In June 2020 a group of us embarked upon a mission to walk 10 Million Steps between us to raise money for 'NF1 Army'. NF1 Army is a fundraising mission I set myself just over a year ago now and it has so far raised just over £12,000. It started out as a personal mission to raise more awareness and support more research after my daughter Jessica was diagnosed with NF1. It has become a real team effort and there is a great sense of community around all of our fundraisers which we really enjoy.
The money we raise will help to fund research at Manchester Children's Hospital as Jessica has been supported by them throughout her life and in the process we are also raising lots of much needed awareness for NF1. I realised early after Jessica had been diagnosed that not enough people have heard of this condition and I am determined to change that and make a difference through the fundraising we do.
'Team 10 Million' has been fantastic.
NF1 Army FaceBook Page![](/images/common/NF1_Army_-_Team_10_Million-1024x768.jpg)
We have been recording and reporting in our steps daily on our Facebook page 'Team 10 Million' and supporting each other along the journey. We've had some amazing achievements and fun with our Wall's of Fame -
30k Steps Wall of Fame
![](/images/common/NF1_Army_30K_Club_Wall_of_Fame_1024x768.jpg)
40k Steps Wall of Fame
![](/images/common/NF1_Army_40K_Club_Wall_of_Fame_1024x768.jpg)
50k Steps Wall of Fame
![](/images/common/NF1_Army_50K_Club_Wall_of_Fame_-_1024x768.jpg)
Most importantly we've been a team and every step really did count. We reached and exceeded our goal and raised over £2000 in the process which we are overjoyed about. I genuinely believe that we can make a positive change if we all come together and start to spread the word.
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