I sadly cannot participate (wrong country), but I hope a lot of patients will do so. The project is hope. Thank you for your work and sharing this topic 🌻.
Thank you for doing this Elinor. I didn't know about it but now I've signed up and completed the questionnaire.. You're an absolute star🌟and your vids have helped me so much xx
Thanks so much for raising awareness of this vital study! I'm unfortunately not able to take part as I'm still waiting for a diagnosis but it's so amazing to see the community coming together to start solving this nightmarish condition.
I would recommend finding a local support group for patients with me/CFS. They probably know how to find a doctor near you who can help. I got my diagnosis from an internal medicine specialist, but that may be different in a different country
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Thank you elinor. I had no idea this was happening and had almost resigned myself to the fact this would never change.
we are getting there!
Looked up "Decode ME" & watched a video called "The most important ME/CFS study EVER? And Taking Part in Decode ME Research!"
Flippin awesome, yay!
I sadly cannot participate (wrong country), but I hope a lot of patients will do so. The project is hope. Thank you for your work and sharing this topic 🌻.
So excited for this study, thank you to all the DecodeME team
Thank you for doing this Elinor. I didn't know about it but now I've signed up and completed the questionnaire.. You're an absolute star🌟and your vids have helped me so much xx
I’m so pleased! Glad it was helpful!
I've also taken part, so grateful it's happening
me too!
Thanks so much for raising awareness of this vital study! I'm unfortunately not able to take part as I'm still waiting for a diagnosis but it's so amazing to see the community coming together to start solving this nightmarish condition.
Ive taken part in this, its a wonderful study
I know! I’m super excited!
I hadn't heard about this study, signing up now!
Yayy!
It great to think that eventually the scientific community are taking this seriously. 😁👏
I know, right?
Great video. I took part in the spit and 2 questionnaires, I’m so excited to see the results
Great interview! And cool earbuds!
Fab to see the octopus taking part too 😁
Glad you enjoyed it! 😂
you are doing amazing work🎉🎉🎉
Thank you so much 😀
Is it worldwide?
No, it's England, Wales, Ireland etc. In the future eventually worldwide (see FAQ on their homepage).
I am from India which test I do for diagonise cfs
I would recommend finding a local support group for patients with me/CFS. They probably know how to find a doctor near you who can help. I got my diagnosis from an internal medicine specialist, but that may be different in a different country