Emily Taylor Interview with WYPR’s Midday
![](https://solvecfs.org/wp-content/uploads/2018/03/emily-e1637691757648.png)
Solve M.E. Vice President of Advocacy and Community Engagement Emily Taylor joins WYPR’s Midday host Tom Hall on Wednesday, December 15, from 12-1 pm ET / 9-10 am PT for a live […]
Watch our H.R. 7057 Town Hall Meeting
![](https://solvecfs.org/wp-content/uploads/2020/09/Co-Sponsor-Graphic-For-Email.png)
Watch now: The H.R. 7057 Legislative Cafe Chat Hosted by Emily Taylor Earlier this year, Representative Jaime Raskin introduced H.R. 7057, the Understanding COVID–19 Subsets and ME/CFS Act. This landmark […]
Solve M.E. Hosts H.R. 7057 Legislative Cafe Chat
![](https://solvecfs.org/wp-content/uploads/2020/12/logo-on-white-1024x1024.png)
Join Solve M.E. for an H.R. 7057 Legislative Cafe Chat on Sept. 9! We’ve received dozens of emails from you asking questions about the historic legislation endorsed by Solve M.E. […]
ME/CFS Advocacy Day 2020 Was the Biggest Ever! Help Us Say Thank You
![](https://solvecfs.org/wp-content/uploads/2021/05/Untitled-design-3-1024x1024.png)
251 Meetings – That’s 47% of Congress! Thanks to the hard work of our advocacy community, Solve ME/CFS Advocacy Day was a wild success! Across the country you called for […]
ME/CFS Advocacy Week Continues: Can You Hear M.E. Now?
![](https://solvecfs.org/wp-content/uploads/2020/04/3Call-3.png)
Can you hear M.E. Now? Call Congress Today! We connected with over 47% of congress yesterday. But we’re not done yet! Today we’re focusing on phone calls to […]
We’re not done, yet! ME/CFS Advocacy Week Ends April 26!
![](https://solvecfs.org/wp-content/uploads/2020/04/stickers_min-1024x578.png)
Looking for a way to make your social media account stand out? We’ve created ME/CFS GIPHY stickers to use on Instagram stories and Twitter, which we think is really easy […]
Solve ME/CFS Advocacy Week ONLINE Schedule is here!
![](https://solvecfs.org/wp-content/uploads/2019/02/EmPower_2019-sq-date.png)
Full Schedule of ME/CFS Advocacy Week Online Events and Actions now available This year our ME/CFS Advocacy Week will take place online from April 19 to April 26, 2020. Stay home, […]
Register for Virtual ME/CFS Congressional Meetings from Home: Deadline Extended for Key States!
![](https://solvecfs.org/wp-content/uploads/2020/04/champion_min-1-1.png)
For our last Advocacy Day event in 2019, many of you joined us in Washington, D.C. to bring your stories to the halls of power and tell the leaders of […]
Solve M.E. Announces 2020 ME/CFS Advocacy Week Virtual Transition in Response to COVID-19
![](https://solvecfs.org/wp-content/uploads/2020/03/Remote-Advo-Week-1800x600-1-1024x341.png)
Solve M.E. Advocacy Week activities this April in Washington, D.C., will be transitioning to entirely remote formats and our team will be cancelling in-person events to protect and preserve the […]
Guest Blog: Dr. Lucinda Bateman on the Discussion Surrounding the IOM Report
![](https://solvecfs.org/wp-content/uploads/2019/04/bateman-2.jpg)
Lucinda Bateman, MD, specializes in the diagnosis and management of unexplained chronic fatigue, ME/CFS and fibromyalgia. Having served on the IOM committee that produced the recent report, Beyond ME/CFS: Redefining an Illness, she brings an in-depth, well-informed opinion to the conversation surrounding the IOM report on ME/CFS, the new diagnostic criteria and the proposed name, Systemic Exertion Intolerance Disease (SEID). READ MORE…
IOM Report Released – Recommends New Diagnostic Criteria, Calls for More Research, and Proposes New Disease Name
![](https://solvecfs.org/wp-content/uploads/2021/07/hans-reniers-lQGJCMY5qcM-unsplash-2-scaled-1-1024x683.jpg)
IOM Report Released – Recommends New Diagnostic Criteria, Calls for More Research, and Proposes New Disease Name. The report underscores the profound impact that ME/CFS has on the millions who suffer from it worldwide (est. 17 million) and the importance of getting people diagnosed; committee calls for more research funding. READ MORE…