We're the Institute for Neuro-Immune Medicine investigating ME/CFS. Support our research and join our study or spread the word! #MECFS#MillionsMissing#CFS
"Millions suffer from an invisible disease" @CNN: https://t.co/tKdRoI8aTS
Help us further our research to find a cure for this invisible disease by donating your 23andme or https://t.co/8qfKx8boqd data, for more information click below:
https://t.co/16m3yZK7kf
#cnn#cfsme
Does folate deficiency play a role in ME/CFS symptoms? NSU is beginning a study to evaluate the role of folate in ME/CFS. Supporting us, donate your 23andMe or https://t.co/ObZhqg8LCS dna to our growing global ME/CFS database. #chronicfatiguesyndrom
https://t.co/16m3yZK7kf
Does folate deficiency play a role in ME/CFS symptoms? NSU is beginning a study to evaluate the role of folate in ME/CFS. Consider supporting us, donate your 23andMe or https://t.co/ObZhqg8LCS dna to our growing global ME/CFS database. #cfsme
https://t.co/16m3yZK7kf
Does folate deficiency play a role in ME/CFS symptoms? NSU is beginning a study to evaluate the role of folate in ME/CFS. Consider supporting us, donate your 23andMe or https://t.co/ObZhqg8LCS dna to our growing global ME/CFS database. #pwme#mecfs
https://t.co/16m3yZK7kf
Does folate deficiency play a role in ME/CFS symptoms? NSU is beginning a study to evaluate the role of folate in ME/CFS. Consider supporting us, donate your 23andMe or https://t.co/ObZhqg8LCS dna to our growing global ME/CFS database. #millionsmissing
https://t.co/16m3yZK7kf
NSU has identified changes in DNA at immune regulatory regions of ME/CFS patients! Consider supporting our research, donate your 23andMe or https://t.co/ObZhqg8LCS DNA to our global ME/CFS gene database. #ChronicFatigueSyndrome
https://t.co/16m3yZK7kf
https://t.co/qN30ogvxBp
NSU has identified changes in DNA at immune regulatory regions of ME/CFS patients! Consider supporting our research, donate your 23andMe or https://t.co/ObZhqg8LCS DNA to our global ME/CFS gene database. #pwme#ChronicPain
https://t.co/16m3yZK7kf
https://t.co/qN30ogvxBp
NSU has identified changes in DNA at immune regulatory regions of ME/CFS patients! Consider supporting our research, donate your 23andMe or https://t.co/ObZhqg8LCS DNA to our global ME/CFS gene database. #invisibleillness
https://t.co/16m3yZK7kf
https://t.co/qN30ogvxBp
NSU has identified changes in DNA at immune regulatory regions of ME/CFS patients! Consider supporting our research, donate your 23andMe or https://t.co/ObZhqg8LCS DNA to our global ME/CFS gene database. #millionsmissing
https://t.co/16m3yZK7kf
https://t.co/qN30ogvxBp
NSU has identified & validated changes in DNA at immune regulatory regions of ME/CFS patients! Consider supporting our research, donate your 23andMe or https://t.co/ObZhqg8LCS DNA to our global ME/CFS gene database. #mecfs#cfsme
https://t.co/16m3yZK7kf
https://t.co/qN30ogvxBp
A special 30% off at https://t.co/iEdgtJdjWl through August 9, 2018. Donate your DNA to help us advance our research into ME/CFS. For more information, click here- https://t.co/16m3yZK7kf
@Borelmedwriter Is it possible to have the NSU gene study posted in this blog? We have nearly 500 patient genetic files which several studies underway from the database we are generating. We hope to grow this global genetic database to 10k ME/CFS patients but need help spreading the word.
NSU is launching new ME/CFS research. We have an expanding genetic database from patients that have donated their https://t.co/ObZhqg8LCS or 23andME DNA. Help us grow, consider donating your DNA file from these sites. #CFS#cfsme#invisibleillness
https://t.co/16m3yZK7kf
@urbantravelsLA @Mishka0808 For healthy controls, we are looking for anyone who has not been diagnosed with ME/CFS. Feel free to share to your friends or on your social media about our study. We haven't been funded yet so this has all been word of mouth. But studies are getting underway!
Thank you @Mishka0808! Because our database has almost reached 500 patients, w'll begin searching for gene mutations this fall. The goal is to have the files of 10k patients, that would yield strong results and get NIH and WHO attention. This database will generate many studies https://t.co/4TFMLejewd
Just submitted my DNA to help with this study. Please consider doing so if you've had an https://t.co/67TKlJo69I or https://t.co/OviJc5w90C DNA test. The larger the database the closer we hopefully will get to solve the MECFS puzzle. https://t.co/40eKZ3gsYv
Our MECFS global genetic database has reached nearly 500 genetic files! If you have ME/CFS, consider donating your https://t.co/ObZhqg8LCS or 23andMe genetic results to our global study. #mecfs#millionsmissing#MyalgicEncephalomyelitis#MEcfs#pwme
https://t.co/16m3yZK7kf