Global Genes LIVE!
09 September 2020
September 15-25, 2020 at Global Genes LIVE! A RARE Patient Advocacy (un)Summit.
Join Global Genes for a variety of engaging and educational online events, meet-ups, workshops and performances.
This two-week event will provide members of the rare disease community, stakeholders, and allies with opportunities to connect and engage with each other through interactive activities paired with educational programming.
This is how the Global Gene’s story began. Friends, family, and supporters of patients who are affected by rare disease started a global community. Trying to understand the confusion, the overwhelming experience of the unknown and the feelings of isolation, realising that no one is alone. Global Gene’s aim is to connect, empower and inspire the rare disease community.
Participants will gain insights about the latest in rare disease innovations, best practices for advocating on an individual and organizational level, and strategic ways to accelerate change.
If you are affected by NF, or are a carer for someone with NF, a NF supporter/advocate you find different programs or sessions that might be of interest to you. There are ways how to get involved or get informed on recent developments.
For more details:
You will be able to watch our movie "Shine A Light on Neurofibromatosis" on the Disorder Channel
Find out more![](/images/common/rare_disorder_channel_global_genes_live1024x768.jpg)
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