Solve M.E.

Join Solve M.E. leadership for our 2026 Community Address. We’ll discuss how we’re thinking about science and advocacy as we approach the midterms (and what comes after), and your role in what comes next. 🗓 Oct 20 · 1 PM PT / 4 PM ET Recorded + captioned Sign up👇 https://ow.ly/sshh50ZREFm

Reminder: Solve’s Ramsay Research Grant Program is open through Friday, Nov. 13! Know an ME/CFS or Long Covid researcher who should apply? Share this with them. Learn more and apply here: https://solvecfs.org/research/ramsay-research-grants/ #MECFS #LongCovid #RamsayResearchGrant

ICYMI: Watch the replay of our Community Address! Learn more about Solve M.E.'s 2026 priorities for advancing research, accelerating treatments, and strengthening community advocacy. https://ow.ly/xilb50ZZVV9 #MECFS #LongCovid #Research #Advocacy

Myth #6: Doctors cannot help people with ME/CFS. ❌ There are no FDA-approved treatments yet, but doctors can help manage symptoms like poor sleep, pain, and heart issues. Swipe to see what the science shows. ➡️ Part 6 of our six-part Myth vs. Fact series. #MECFS

Sign up! Our friends at Brain Inflammation Collaborative are hosting a free live webinar on inflammation and hypermobility in #LongCOVID, #MECFS & #MCAS. 🗓️ Thurs 10/29, 3pm ET / 12pm PT Register here: https://ow.ly/i5HE50ZZW1K

Myth #5: Long Covid is entirely different from ME/CFS. ❌ Many with Long Covid meet the diagnostic criteria for ME/CFS, including PEM, its main symptom. Swipe to see what the science shows. ➡️ Part 5 of our six-part Myth vs. Fact series. #MECFS #LongCovid #ChronicIllness #MEAwarenessHour

Researchers, do you have questions about your Ramsay Grant application or the submission process? Join us for an informal Q&A with the Solve M.E. team, Thurs., Oct. 22 | 8:00 am PT / 11:00 AM ET Bring your questions—we're here to help! Register: https://ow.ly/Emu050ZYeTM

Myth #4: Only certain groups of people develop ME/CFS. ❌ Fact: ME/CFS can affect anyone, regardless of race, gender, age, or income. Disparities in diagnosis and access to care mean many people go unrecognized. Part 4 of our Myth vs. Fact series. ➡️ #MECFS #HealthEquity

⏰Starting soon! Join us today @ 1 pm PT / 4 pm ET, for "The Solve 2026 Community Address: Shaping What Comes Next." We’re rolling out our plan for the whole year re: science and advocacy, your role in it, and how we win together. Register: https://ow.ly/LitX50ZZ23K

Myth #3: You can exercise your way to recovery from ME/CFS. ❌ Fact: Exercise was once prescribed for ME/CFS, but the guidance has changed. Pushing through can make symptoms worse. Experts now recommend pacing instead. Part 3 of our Myth vs. Fact series. ➡️ #MECFS #Pacing

Multiply your impact 4X! Thanks to two generous donors and our Board of Directors, all gifts to Solve M.E. will be matched 4X through November 30, up to $250,000. Your $25 becomes $100, $100 becomes $400! Give today: https://solvecfs.org/donate/ #MECFS #InvisibleIllness #MatchingGift

📣Join us Tues, Oct. 20 @ 1 pm PT / 4 pm ET, for "The Solve 2026 Community Address: Shaping What Comes Next." We’re rolling out our plan for the whole year re: science and advocacy, your role in it, and how we win together. Register: https://ow.ly/PLmI50ZZ25p

⏰ Just one day left! The CDC's proposed 2028 survey could leave millions of people with ME/CFS and Long Covid uncounted. Solve is speaking up. You can, too. Submit your comments by October 19! Check out the link below for details: solvecfs.org/cdc-me-cfs-long-covid-survey/ #MECFS #CDC

Myth #2: ME/CFS is just about feeling tired. ❌ Fact: The defining symptom, Post-Exertional Malaise (PEM), is far more than fatigue. Even small physical or mental effort can trigger a crash lasting days or longer. Part 2 of our Myth vs. Fact series. ➡️ #MECFS #PEM

The CDC's proposed 2028 survey could leave millions of people with ME/CFS and Long Covid uncounted. Solve is speaking up. You can, too. Submit your comments by October 19! Check out the link below for details: https://solvecfs.org/cdc-me-cfs-long-covid-survey/ #MECFS #CDC #HealthAdvocacy

Myth #1: ME/CFS is a mental health condition. ❌ Fact: ME/CFS is a serious biological illness that affects the body’s core systems. For millions, it upends the ability to work, study, or even leave home. Part 1 of our Myth vs. Fact series. ➡️ #MECFS #ChronicIllness

ME/CFS is widely misunderstood, and those misconceptions can have real consequences for people living with the disease. Swipe through as we separate some of the most common myths about ME/CFS from the facts. ➡️ #MEAwarenessHour #MECFS

Researchers at FHCSD seek patients diagnosed or w/ symptoms of Long Covid for the LC-Revitalize treatment study. Participation spans 6 mos, w/8 visits (6 in-person @ a San Diego-based clinic). Contact researchers @ longcovid@fhcsd.org / (619) 324-8677 for more info or to join.

Sign up for our Nov. 10 webinar on the Renegade Research SIGNAL study. We’ll discuss how people with #MECFS and #LongCovid can join and borrow therapeutic devices for home use at no cost & contribute data to the BIC unhide® platform for research. Register: https://ow.ly/LGx250ZIvx7

Solve’s Ramsay Research Grant Program is open for submissions! Visit our website for more information about the types and amounts of awards and how to apply by the November 13 deadline. https://solvecfs.org/research/ramsay-research-grants/ Please share this news with your network!

📣Big news from Solve’s research team re: an upcoming funding opportunity for researchers studying #MECFS, #LongCovid, and associated conditions! Stay tuned for more info on October 6 & click the link to learn more about our Ramsay Research Grant Program. https://ow.ly/WnOh50ZUEte

Sign up for our Nov. 10 webinar on the Renegade Research SIGNAL study. We’ll discuss how people with #MECFS and #LongCovid can join and borrow therapeutic devices for home use at no cost & contribute data to the BIC unhide® platform for research. Register: https://ow.ly/LGx250ZIvx7

Today, we're celebrating advocacy in action! Advocate & caregiver to her son, Gabe, Rebecca Groble secured an Illinois Senate Resolution acknowledging the prevalence & impact of ME/CFS across the state. Thanks, Rebecca, for your dedication to raising awareness! #MEAwarenessHour

Our IVO-21 webinar with Dr. Jay H. Chung was recently featured in Health Rising! Read the full article to learn more about the research supported through Solve's Catalyst Award: https://ow.ly/V4yE50ZSnHT Watch the webinar: https://ow.ly/WI3i50ZSnI1 #MECFS #ChronicFatigueSyndrome #IVO21

Join Solve M.E. leadership for our 2026 Community Address. We’ll discuss how we’re thinking about science and advocacy as we approach the midterms (and what comes after), and your role in what comes next. 🗓 Oct 20 · 1 PM PT / 4 PM ET Recorded + captioned Sign up👇 https://ow.ly/sshh50ZREFm

Sign up for our Nov. 10 webinar on the Renegade Research SIGNAL study. We’ll discuss how people with #MECFS and #LongCovid can join and borrow therapeutic devices for home use at no cost & contribute data to the BIC unhide® platform for research. Register: https://ow.ly/LGx250ZIvx7

Today at 3 pm PT / 6 pm ET! Join us for a free webinar with Brain Inflammation Collaborative (BIC) to discuss how using the unhide® real-world data platform can help you recognize health patterns & trends to support conversations with healthcare providers. Register here: https://ow.ly/o1Iq50ZyLBO

Today is the last day to comment on a proposed reorganization by the National Inst. of Allergy & Infectious Diseases (NIAID) eliminating its Div. of Clinical Research--the infrastructure behind clinical trials. Learn how to share your own comments: https://ow.ly/GI7N50ZOWV0

Join us on 9/22 for a free webinar with Brain Inflammation Collaborative (BIC) to discuss using the unhide® real-world data platform to recognize health patterns & trends to support conversations with healthcare providers. Register here: https://ow.ly/o1Iq50ZyLBO

📣Tomorrow is the last day to publicly comment on a proposed reorganization by the Natl. Inst. of Allergy & Infectious Diseases (NIAID) eliminating its Division of Clinical Research — the infrastructure behind clinical trials. Learn how to share your own comments hree: https://ow.ly/1EnG50ZOWXS

Sign up for the CDC ME/CFS Stakeholder Engagement & Communication (SEC) Call - 'How Progress in Long COVID is helping us understand ME/CFS,' w/ Dr. Nancy Klimas + program updates from CDC's ME/CFS program staff & a Q&A. Fri., Sept. 18, 2026, 12-1:30 PM ET / 3-4:30 pm PT. https://ow.ly/jCMK50ZMVux

Family Health Centers of San Diego (FHCSD) seeks patients diagnosed with or have signs & symptoms of #LongCovid to join the treatment study"LC-Revitalize." Participation spans 6 mo, with 8 visits (6 in-person @ a SD- based clinic). To join or learn more: longcovid@fhcsd.org or (619) 324-8677.

ICYMI: Watch the recording of our webinar with Dr. Jay H. Chung re: his Catalyst Award-winning study of the mitochondrial stabilizer IVO-21 as a therapy for #MECFS. https://ow.ly/Hfp450ZLzT3 #MEAwarenessHour

Starts today at 3 pm PT / 6 pm ET! Join our webinar with Dr. Jay H. Chung (NIH), who will discuss his Solve ME/CFS Catalyst Award-winning study of a potential safe and accessible treatment for #MECFS. https://ow.ly/ONZA50YZ8jn

Sign up for our Nov. 10 webinar on the Renegade Research SIGNAL study. We’ll discuss how people with #MECFS and #LongCovid can join and borrow therapeutic devices for home use at no cost & contribute data to the BIC unhide® platform for research. Register: https://ow.ly/LGx250ZIvx7

Congress voted to delay through Dec. 11 a rule that lets political appointees cancel federal grants, incl. active clinical trials, overriding the peer review process. We fought for this delay, now ask Congress to end the rule permanently. Use our toolkit: https://ow.ly/xQtc50ZIrwH

We’re saddened by the passing of Dr. Jo Cambridge, a valued member of Solve’s research network and a 2016 Ramsay Research Grant recipient whose work advanced our understanding of ME/CFS. Read more about Dr. Cambridge and her work: https://ow.ly/MgKi50ZI0Uc

ICYMI: Solve recently joined host Bateman Horne Center and #MEAction Network, Open Medicine Foundation (OMF) & the WIMEL Writers for "Coffee with a Clinician" in honor of #SevereMEAwareness Month. Watch the replay here: https://ow.ly/x9Sy50ZGmU6 #UnitedForME