solveme
- 💙 Huge THANK YOU to Senator Bill Cassidy for prioritizing ME/CFS & Long COVID in today's HELP Committee Hearing. His first question was dedicated to the urgent need for research & federal support for these conditions. 🙌 #MECFS #LongCOVID
- 🌟 Your Voice Can Save ME/CFS Research! 💙 The CDC Chronic Fatigue Syndrome Program—the only federal effort dedicated to ME/CFS research and public health—is at risk of being cut. Losing it would be a devastating setback for millions of Americans living with ME/CFS.
- 🚨 Action Alert: Help Restore Critical ME/CFS Research Funding! 🚨 Congress slashed CDMRP funding by 57%, putting life-saving ME/CFS research at risk. We need your help to restore it. 👉 Take Action Now: solvecfs.quorum.us/campaign/124... 🧵 Details in the thread below: #RestoreOurResearch #pwME
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- In honor of #WorldMEDay we're announcing the Solve #MECFS Catalyst Awards—fast-tracking bold research w/over $100k in funding when it matters most. Congrats to our first winner @virusesimmunity.bsky.social (@yaleschoolofmed.bsky.social)on her game-changing autoantibodies study! ow.ly/vVfa50VRaBL
- 🚨 Big news! Every dollar you give to Solve M.E. by June 30 will be matched up to $50,000! Your gift powers research, advocacy & education. Together, we can accelerate progress!💪 🧬 Please give today: ow.ly/F0B250VOafC #MECFS #MEAwarenessMonth
- Reposted by solvemeExcited to share our Opinion piece on "How to Lead a Chronic Disease Revolution" with Harlan Krumholz Hint: study infections & immune responses as a catalyst for chronic diseases like neurodegenerative, autoimmune, cancer, and many more. www.wsj.com/opinion/how-...
- 🎥 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 @rivkabluesky.bsky.social & @themegascope.bsky.social, is online now. Watch here: youtu.be/2DQZp48fyek
- May is #MEAwarenessMonth & 5.12 is #WorldMEDay! Let's change the narrative around #ME & get the facts right! Help challenge myths & champion facts w/the @WorldMEAlliance custom poster maker!💙 ow.ly/vRpW50VLrB6 #MEAwareness #MECFS
- Solve, the Brain Inflammation Collaborative, ChronicleBio, the Complex Disorders Alliance, and CareEvolution launch a historic partnership to accelerate ME/CFS, Long Covid & IACCI research! More data, faster breakthroughs. Learn more: ow.ly/cVih50VJT2f #ChronicIllness #LongCovid #MECFS #Research
- There's still time to register for today's 3 pm PT/6 pm ET webinar "Investigating Immune Dysfunction & T-Cell Exhaustion via Single Cell Immune Profiling in #MECFS & #LongCOVID," w/panelists Selin Lab and HiFiBio. Register here: ow.ly/4Spj50VumTk
- Register for our April 29 (3 pm PT/6 pm ET) webinar "Investigating Immune Dysfunction & T-Cell Exhaustion via Single Cell Immune Profiling in #MECFS & #LongCOVID," w/ Liisa Selin, PhD (Selin Lab), Roshan Kumar (HiFiBio), Megan Fitzgerald, PhD, & Rivka Solomon, M.S. Sign up: ow.ly/4Spj50VumTk
- In the lead-up to #WorldMEDay on May 12th, the @WorldMEAlliance highlights 6 pervasive myths surrounding ME & the facts that challenge them. Read more here: ow.ly/EPQT50VCvFq #WorldMEDay #Fact #FactOfTheDay #MyalgicE #MECFS
- 🚨Advocacy Alert! 🚨 Congress cut CDMRP funding by 57%—devastating for ME/CFS research. We’re fighting back—but we need your voice. 📢Tell Congress: Restore CDMRP funding in FY26! 🔗Take Action: ow.ly/H9xM50VB7wJ #MECFS #CDMRP #restoreCDMRP
- ME/CFS San Diego announces winners of the 2024 UCSD Graduate Student ME/CFS essay contest! 🎉 🏆 1st place: Emily Lam 🥈 2nd place: Benjamin Lam. Learn more here: www.mecfssandiego.com/mecfs-san-di... #MECFS #MEAwareness
- Thanks to @maxkozlov.bsky.social and @nature.com for speaking to Solve President Emily Taylor about the devastating impact of funding cuts for #LongCovid research and the work of advocates to get funding restored.
- ICYMI: Solve CEO Emily Taylor spoke to AirTalk with Larry Mantle (KPCC/LAist) about the impact of recent cuts to #NIH funding for #LongCovid research, including the Department of Defense #CDMRP program. Listen here: ow.ly/MARH50Vtwug
- ICYMI: "Crazy Times: Trump Administration Pulls Millions of Dollars From Long COVID Grants (and Then Restores Them?) Plus ME/CFS, Antiviral, Vaccine Funding Hit" from Cort Johnson and Health Rising www.healthrising.org/blog/2025/03...
- 🚨 Matching Gift Challenge!🚨 Every $1 you give TODAY is doubled—up to $10K! Help us fund critical ME/CFS & Long Covid research and education. Deadline: MIDNIGHT! Donate now & double your impact! ow.ly/20Kg50VoAYx #MECFS #LongCOVID #DonateNow
- Now! On KPCC's AirTalk with Larry Mantle, Solve CEO Emily Taylor talks about #LongCovid. Tune in here: ow.ly/q5vP50VrLu2
- Solve CEO Emily Taylor talks to Fierce Biotech about critical funding cuts threatening #MECFS research, the need for sustained NIH investment, and how #LongCOVID could reshape the field. #BiomedicalResearch ow.ly/FsTk50VrGX7
- Solve M.E.'s Research Grants fund studies to uncover causes & treatments for #MECFS & #LongCovid, & Advocacy Week educates Congress for action. Please support our work w/ a gift today. Donate by April 1 & your gift will be doubled thanks to our $10k match challenge! 💙 Give here: ow.ly/IhN550VoAYy
- Tell your members of Congress to reverse the 57% cut to the Congressionally Directed Medical Research Program! Congress cut funding by 57%--from $1.509 billion to $650 million & ME/CFS research will receive $0 in FY25. Use our toolkit to take action now: ow.ly/Cixp50VnNNK #RestoreOurResearch
- NEW STUDY! The Metrodora Institute seeks participants to join the MELO Study to evaluate biomarkers in #MECFS & #LongCOVID. Participation is free & voluntary for adults 18+ in the US. No clinical diagnosis of ME/CFS or LongCOVID is required. Sign up here: ow.ly/kJYe50Vkfuy
- We are proud to announce the new members of the Solve M.E. 2025-26 Lived Experience Taskforce (LET)! These community partners are affected by #MECFS or #LongCovid and help shape our initiatives with the authenticity of lived experience. Learn more here: ow.ly/32gx50VmqP4
- 🚨 DOUBLE YOUR IMPACT! 🚨 A generous donor is matching all gifts up to $10K—now through April 1! Your donation fuels advocacy, research, and hope for millions. Let’s hit $10K together! Every $1 you give = $2! 💙 Click this link to donate today: ow.ly/Wfx150VjypJ
- Thank you AARP magazine for your piece on the devastating impact of #COVID on adults over 50. The article features Solve M.E. Long Covid Patient Leadership Advancement Network (LC-PLAN) advocate Cathy Mesa. ow.ly/HW9l50ViApK #LongCovid #LongCovidAwarenessDay #LongCovidAwarenessDay2025
- Today is #LongCovidAwarenessDay! We stand in solidarity with over 400 million worldwide living with #LongCovid. Let's raise awareness, push for action, and ensure no one navigating Long Covid feels invisible. Get info on Long Covid Awareness Day actions and events here: ow.ly/YiaK50ViozE
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- URGENT ACTION UPDATE! Sen Coons & Sen. Alsobrooks have filed amendments on behalf of the CDMRP program. Tell your Senators to vote YES on the Coons and Alsobrooks amendments to prevent a 57% cut to CDMRP and fully fund the program in fiscal year 2025. ow.ly/FvbL50VijLt
- Registration is now open for Solve’s Virtual Advocacy Week, June 23-27, 2025! Make your voice heard – help educate Congress about ME/CFS and associated conditions. Register by May 12 at MEForward.org. #MEForward
- URGENT! The Senate is considering a 57% cut to DoD's Congressionally Directed Medical Research Program (CDMRP)--including $ for a program that provides millions of research dollars for #MECFS. Click here to tell your Senators no cuts, full funding! ow.ly/MZLT50Vfix5 #MEAwarenessHour
- The Socially Conscious Lab @ Rosalind Franklin University of Medicine & Science seeks study participants ages 18+ who've had long symptoms of COVID-19 for 3+ months. Participants will complete online questionnaires about mood & behavior. Learn more: rosalindfranklin.qualtrics.com/jfe/form/SV_...
