ICYMI: Watch our webinar “Repurposing Rapamycin: A Report On the First Biomarker-Driven Treatment Trial for ME/CFS,” with Dr. Gunnar Gottschalk, Dr. Avik Roy & Courtney Alexander from Simmaron Research https://youtu.be/oJnUW-B089I #MEAwarenessHour

Starting soon! Register for our free webinar, “Repurposing Rapamycin: A Report On the First Biomarker-Driven Treatment Trial for ME/CFS,” with the Simmaron Research team. Today, July 14, @ 3:00 pm PT / 6:00 pm ET. https://ow.ly/jsrZ50Zg3CA

If you were a participant in the Vyvgart trial, please email Mackenzie at coreresearch@mountsinai.org to get a free at-home lab kit. Mt. Sinai & Yale are testing against a newly discovered autoimmune biomarker, with the goal of initiating a new FCRN inhibitor trial by year-end!

🚨 DEADLINE TODAY: Proposed federal regulatory guidance would let political appointees override scientific peer review & terminate active research grants with no finding of wrongdoing. ME/CFS & Long COVID research is on the line. Submit a public comment before tonight 👇 https://ow.ly/rtlb50Zn4T9

Building on our 2026 Advocacy Week efforts, Solve, #MEAction Network, Bateman Horne Center, and a local constituent had a productive meeting with the Montana Board of Medical Examiners to discuss #MECFS medical education. Learn more: https://ow.ly/U3uz50ZlLNi #MEAwarenessHour #UnitedForME

You don't have to name it to know it's a lot. Get your Caregiver Intensity Score from @ARCHANGELS.ME — quick, free, and built to point you to the things that can help. https://archangelscii.me/4wkc5CM

We filed our public comment this week on the federal regulatory guidance that will shape how research gets funded and managed. 1/5

📢A proposed federal rule could let the government cancel active #MECFS research mid-study when political priorities change. The public comment window closes July 13. Take action: https://ow.ly/J5EP50ZcpV0 How to submit a public comment: https://ow.ly/Oq6150ZcpUZ Please share! #MEAwarenessHour

Because of you, we met our $200,000 fundraising goal! Our research and advocacy programs are only possible with the support of our community. Thank you so much for your trust and partnership!

Just a few hours left to join our $200,000 matching gift challenge! Help move #MECFS and #LongCovid science forward with a gift to Solve M.E. https://solvecfs.org/donate/

Researchers are identifying disease pathways and discovering biomarkers that could lead to effective treatments. But promising science only changes lives when it's funded. Give to Solve before our $200k match ends at midnight to double your impact! https://solvecfs.org/donate/

These numbers represent real progress & hope for millions living with #MECFS & #LongCovid. Solve M.E. has driven breakthroughs, but there's so much more to do. Help us write the next chapter.  All gifts made by midnight 6/30 will be doubled up to $200k! https://solvecfs.org/donate/

Community member Tina shares her story and explains why she supports the work of Solve M.E. Make a gift to Solve today. All donations to Solve through June 30th will be matched up to $200,000! https://solvecfs.org/donate/

Two recently published studies funded by Solve point to gastrointestinal dysfunction as a key driver of illness in people with ME/CFS. Their results support precision medicine approaches and create pathways to better treatments. Learn more: https://ow.ly/v5bX50ZgImV

🚀 Solve Ramsay Grant winner Dr. Lubov Nathanson & team secured a $3M NIH grant for #MECFS research! Solve funds scientists like Dr. Nathanson so pilot studies can become multimillion-dollar research programs. Accelerate research w/ a gift to Solve! https://solvecfs.org/donate/

Solve M.E. VP of Scientific Programs Dr. Jessica Maya & Advocacy Dir. Monique Wike are in San Diego this week for the 2026 BIO Convention. The focus this year is on solving the impossible, pushing boundaries, & delivering better outcomes. If you see them, say hello! #BIO2026

If you’re the one paying for everyone’s everything, that can increase intensity. Get your Intensity Score from ARCHANGELS.ME — takes 2 minutes, and you'll get matched to free resources that can help with money and anything else you're carrying right now. https://archangelscii.me/3Qg9ydA

Our ME/CFS Catalyst Award & Ramsay Research Grant Programs wouldn’t be possible without community support. With your help, we can turn hope into real progress. Help fund breakthrough studies with a gift to Solve today. All gifts will be matched up to $200k through 6/30! https://solvecfs.org/donate/

Watch now! View the recording of our webinar "Sequence ME & #LongCovid: The Search for #MECFS and Long Covid Biomarkers and Subtypes," featuring the DecodeME Management Team. https://youtu.be/v6VQ2593m-8

1/ A proposed federal rule could let the government cancel active ME/CFS research mid-study when political priorities change. The public comment window closes July 13. Here's what you can do 🧵

Join us for a webinar this Wednesday with panelists from DecodeME and ActionForME to discuss their Catalyst Award-winning study on Sequence ME and Long Covid and how it could impact the search for #MECFS & #LongCovid biomarkers and subtypes. https://ow.ly/x0fJ50YZ86w

With your support, Solve can fund studies that bridge the gap between research and clinical trials, and help scientists move closer to testing new therapies in people with #MECFS and #LongCovid. All gifts made through June 30th will be DOUBLED up to $200,000! https://solvecfs.org/donate/

With your help, we can turn momentum into real breakthroughs. Your gift to Solve today supports studies that can translate discoveries into treatments. And now, all gifts made through June 30th will be matched up to $200,000! https://solvecfs.org/donate/

Wed. 6/3 at 10 am PDT / 1 pm EDT, Kantor & Kantor @ Workwell Foundation offer a free webinar: "Proving Disabling Post-Exertional Malaise and Fatigue: Understanding Disability Benefits and the Two-Day CPET." Register here: https://ow.ly/A4NP50Z2Yva

Register for our Sept. 8 webinar with Dr. Jay H. Chung (NIH) discussing his Solve ME/CFS Catalyst Award-winning study of a potential safe and accessible treatment for #MECFS. https://ow.ly/ONZA50YZ8jn

🚨 BIG NEWS: Our Matching Challenge has been extended to June 30—and increased to $200,000! 🎉 Your gift today will go TWICE as far to support #MECFS + #LongCovid research and accelerate real breakthroughs for millions. Donate now: https://solvecfs.org/donate/

The Brain Inflammation Collaborative will host Dr. Leonard Jason & Anvita Guda for a webinar on #MECFS & brain inflammation, cognitive dysfunction, and patient-centered research on 5/21 @ 2:00 PM CT/3:00 PM ET. Sign up: https://zoom.us/webinar/register/WN_NBLdyA43TESuWA9BUrHufQ#/registration

During Advocacy Week 2026, we asked Congress to keep #MECFS as an eligible topic area in the Congressionally Directed Medical Research Program (#CDMRP). Read the case we made for why ME/CFS is a military issue: https://ow.ly/Gyug50YZQ0P

Check out the LA Weekly feature on Solve CEO Emily Taylor. The piece highlights how caregiving for her mother informs Emily's commitment to accelerating research breakthroughs and the creation of our ME/CFS Catalyst Awards Program. https://ow.ly/yv6H50YZQKq

This week, advocate Rebecca Groble shared information about ME/CFS at the Evanston Public Library in honor of World ME Month. Thank you, Rebecca, and health librarian Irene, for doing your part to educate people about this disease. Visibility matters! #WorldMEDay #UnitedForME