The most important ME/CFS study EVER? And Taking Part in Decode ME Research!

In this video I participated in the Decode ME study by supplying my DNA sample through the spit kit and discussed the aims, values and process of the research with a member of the Decode ME team and fellow ME/CFS patient Anna (@teapartyform.e on Instagram).
This study is a very important first step into the research of the widely misunderstood illness of ME/CFS which has the potential to change opinions and open doors to further research in the future!!


Find out more about Decode ME (and sign up!!)
Website: https://www.decodeme.org.uk/
Initial Findings: https://www.decodeme.org.uk/initial-f...
YouTube: https://youtube.com/@decodeme6153?si=...
Instagram: @decodemestudy




Reminder: everyone with ME/CFS is different! So you or someone you know might have a very different experience with ME/CFS than I do at the moment! Also, remember that chronic conditions such as these can change dramatically over time, so my life may look very different to this in the future (and has be A LOT worse in the past).

Thank you so much for watching!! Make sure to like, comment, and subscribe to see more videos from me most FRIDAYS!



About Me:

My name is Elinor, I am a 24-year-old sociology graduate who has been living with ME/CFS for 8 years. I also have anxiety and depression as co-morbid conditions! I started making YouTube Videos consistently about my experience with chronic illness and mental health struggles in June 2020! I also love fashion, connecting with people in the community and being creative!!



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Social Media:

Follow me on Instagram   / ellellell_brown  




Contact Me:

Direct Message me on Instagram   / ellellell_brown  

For Business enquiries [email protected]





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#Myalgicencephalomeylitis

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