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1:00
YouTube
Genomics England
How can genomics help us understand rare conditions?
Jamie Ellingford, Lead Genomic Data Scientist for Rare Disease at Genomics England, explains how genomics can help us understand rare conditions. Want more detail? Listen to our podcast, where Jamie goes into more detail, in less than 10 minutes. Listen in full via the linked video, or on our website at https://www.genomicsengland.co.uk/podcasts/
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In honour of today being Rare Disease Day, I'm sharing part of my story. ❤️🩹🦓🎗️ I was diagnosed with a rare bone tumor called Giant Cell Tumor (GCT), a one in a million, aggressive tumor that destroyed my upper spine and left lifelong deficits. Sharing this isn't easy, but awareness starts with our stories. We need more research, more understanding, and more voices for those navigating the unknown. Thank you for being part of my journey as I continue to navigate life after GCT. 🫶 #raredisea
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It’s rare disease day and around 300 million people live with a rare disease including 1 in 5 people with cancer. A disease is considered rare if it impacts less than 2000 people #raredisease #zebra #doctor #rarediseaseawareness #showyourstripes Disclaimer: For educational and entertainment purposes only and should not be regarded as medical advice or replace the advice of your physician
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