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/Hannah_1_370x280_800_600_s_c1.jpg)
Hannah’s NF1 story
9 year old Hannah is running the Junior Great North Run, so other children with NF can also have access to doctors & nurses
Read More![](https://nervetumours.org.uk/images/made/images/common/Sam_Gaden_marathon_2_370x280_800_600_s_c1.jpg)
Sam’s Marathon
Sam, our Specialist NF Nurse for Merseyside & the North West, is running the London Marathon - her very first Marathon!
Read More![](https://nervetumours.org.uk/images/made/images/common/2022_Manchester_370x280_800_600_s_c1.jpg)
NF Patients Community Day
The NF Patients Community Day is on Sunday 9th October 2022 - register to attend virtually
Read More![](https://nervetumours.org.uk/images/made/images/common/Naomi_Marshall_Prof_Heather_Widdows_Susan_Ross__Chrissie_from_CF_370x280_800_600_s_c1.jpg)
Appearance, Identity & Law workshop
Appearance, identity & law workshop at Queen Mary University London School of Law
Read More![](https://nervetumours.org.uk/images/made/images/common/image8_370x280_800_600_s_c1.jpg)
Alfred the Pirate
Seven year old Alfred the Pirate takes NF1 in his stride, and is supported by Specialist NF Nurse Mel
Read More![](https://nervetumours.org.uk/images/made/images/common/Nicole_370x280_800_600_s_c1.jpg)
Nicole’s NF1 story & skydive
Nicole shares her NF1 journey and her motivation to inspire children with disabilities to achieve whatever they want to do
Read More![](https://nervetumours.org.uk/images/made/images/common/photo_collage_370x280_800_600_s_c1.jpg)
Sarah’s NF1 story & Langmead fundraising
Sarah describes her daughter Hannah's NF1 journey and organising a corporate charity day fundraiser at Langmead Herbs
Read More![](https://nervetumours.org.uk/images/made/images/common/Molly__Alfie_370x280_800_600_s_c1.jpg)
Molly & Alfie
Mollie has NF1 - her big brother Alfie & friend Kaelan are running to raise awareness & funds for NTUK
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