ME/CFS Research Network
@TheMECFSNet
@NIH-funded network that fosters collaborative research in partnership with individuals and advocacy groups to improve the diagnosis and treatment of #MECFS.
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💞November is National Family Caregivers Month, a time to honor those who give so much of themselves to support loved ones. To every caregiver supporting someone with #MECFS, you are the quiet heroes behind every act of care.
📢Mark your calendars! for the @ICanCMEResearch Canadian Collaborative Conference on Myalgic Encephalomyelitis - Nothing About Us Without Us; November 4-6, 1-5pm ET. This 3 day event is free to register and virtual to attend. Register today: ow.ly/XjSF50XlgbF
📢Attention researchers! Data from @CornellMECFS's study on circulating cell-free RNA signatures in #MECFS is available now on #mapMECFS. #MECFS #MECFSnet Apply for access today: ow.ly/fMj450XjRVv
🎉Exciting news! The newly modernized #searchMECFS tool is live! The redesigned tool offers an enhanced user experience and helps investigators easily find #MECFS biospecimens for use in their research. Explore now: ow.ly/gHjO50XhNXK
🎉The wait is over! The #IACFSME2025 Virtual Conference kicks off today! Researchers, clinicians, and advocates from around the world are coming together to advance understanding of #MECFS and accelerate research and progress towards better diagnosis, treatment, and care.
🌍✨Today we honor the resilience of those living with #MECFS and the importance of mental well-being for everyone. Let's continue to show compassion, share support, and check-in with one another.
✨It's here! The latest #MECFSnet Newsletter is live. Find out what we've been up to. #MECFS #PwME #ResearchCollaboration 👉ow.ly/wjNl50Xa28o
✨Exciting news! New research highlights AI tool that detects #MECFS with 90% accuracy. Congrats to our legacy partners at @jacksonlab! nature.com/articles/s4159…
Heard the news? DecodeME #MECFS Study released initial genetic results! Discover what it means for ME/CFS. Summary of findings: ow.ly/n7Hz50WFrwL Preprint publication: ow.ly/MS1W50WFrwN FAQs: ow.ly/gjqa50WFrwM
🗓️Don't forget to register for tomorrow's DecodeME - Genetic Results Webinar! Link: us02web.zoom.us/webinar/regist…
Join us TOMORROW for our genetic results webinar! Register here: shorturl.at/fnB67 There are limited spots to join on Zoom (registering does not guarantee a spot). Don’t worry though, we will be recording it and we will also be sharing it live on Facebook at the time.
Join us TOMORROW for our genetic results webinar! Register here: shorturl.at/fnB67 There are limited spots to join on Zoom (registering does not guarantee a spot). Don’t worry though, we will be recording it and we will also be sharing it live on Facebook at the time.
📢Research news! The #MECFS Research Network Investigator Meeting convened @NIH leaders and network members @CfSforMECFS, @CornellMECFS, @ICanCMEResearch, and @RTI_Intl's DMCC for study updates on August 4. Collaboration fuels discovery! #MECFSnet #PwME #LongCOVID
🔎Looking for accurate summaries of published #MECFS research? Check out the ME/CFS Research Chatbot! It relies solely on PubMed abstracts. Also access data table with abstracts. S/O to Tracy Duvall for creating this new tool!
📢Research news! New study from #MECFSnet partners @CornellMECFS. Post-exercise changes in extracellular vesicles reveal biological disruptions in men with #MECFS. Read full study! ow.ly/WK6150Ws3Ex
🇺🇲Today we honor and remember the brave men and women who made the ultimate sacrifice for our country.
🎥 The recording of "Investigating Immune Dysfunction & T-Cell Exhaustion via Single Cell Immune Profiling in #MECFS & #LongCOVID," w/panelists from @Selin Lab, @HiFiBio, & patient reps @Rivkatweets & Dr. Megan L. Fitzgerald, is online now. Watch here: youtu.be/2DQZp48fyek
🤝 Accelerate Research: OMF StudyME is a free global participant registry bridging the gap between individuals living with #MECFS, #LongCOVID and related diseases, and the researchers working tirelessly to uncover effective treatments. 👉Sign up today: omf.ngo/studyme/.
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