The Solve ME/CFS Initiative (Solve M.E.) wants to be helpful to all those interested in telling the story of myalgic encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) – traditional journalists, social media writers, and anyone working on sharing the reality of ME/CFS. Interviews with Solve M.E. spokespeople, expert sources working in ME/CFS research and connections to ME/CFS patients can be arranged upon request.

The ME/CFS community prefers to use “myalgic encephalomyelitis,” “ME” or “ME/CFS” when referring to this devastating illness. “Chronic Fatigue Syndrome” is no longer the commonly accepted terminology.

If referring to the illness as “Chronic Fatigue Syndrome,” we recommend using capital letters. We feel it’s important to distinguish this disabling disease from “fatigue” that can be a symptom of many different chronic health conditions. We request that you follow these terminology guidelines when you are quoting Solve M.E. or referencing our information.

MEDIA CONTACT
Email Karman Kregloe at KKregloe@solvecfs.org or call 704-364-0016 (office).

Media Tools

  • Solve M.E.: Leading the Fight to Cure ME/CFS — PDF
  • Solve M.E. Advocacy & Research Programs – PDF
  • Solve M.E. Media Contacts – PDF
  • ME/CFS Fact & Figures Sheet – PDF
  • ME/CFS FAQ — PDF
  • Solve M.E. Op-Ed in the Guardian: “We Know Too Little About Covid-19 ‘long-haulers.’ We Need a Comprehensive Study” – PDF
  • Solve M.E. Position Statements and Letters

RECENT PRESS RELEASES

  • 02.25.21 – Solve M.E. Spearheads Long COVID Alliance to Accelerate Post-Infectious Research – PDF
  • 12.04.20 – Chronic Disease Stakeholders Join Solve M.E. in Push for Federally Funded Research into Long COVID – PDF
  • 08.11.20 – Bipartisan Women’s Caucus to Collaborate with Chronic Illness Nonprofits and Prominent Guests for Virtual, Educational Roundtable Concerning the Impact of Covid-19 on Women’s Health – PDF
  • 07.13.2020 – Solve M.E. Announces Launch of You + M.E. Registry and Biobank  – PDF
  • 05.21.20 – Solve M.E. Announces Oved Amitay as President and Chief Executive Officer – PDF
  • 04.21.2020 – 2020 ME/CFS Advocacy Day – PDF
  • 05.17.2018 – 2018 ME/CFS Advocacy Day – PDF
  • 05.01.2018 – 2018 Ramsay Award Medical Research Program – PDF
  • 10.31.2017 – Ramsay Award Program 2017 Recipients – PDF
  • 10.19.2017 – 2017 ME/CFS Discovery Forum – PDF
  • 09.28.2017 – Solve ME/CFS Initiative Honored to partner on three NIH-funded centers – PDF
  • 09.22.2017 – Circle Receptions in Minnesota – PDF
  • 05.29.2017 – 2017 ME/CFS Awareness Rally-Sacramento – PDF
  • 05.08.2017 – 2017 ME/CFS Advocacy Week in D.C. – PDF

RECENT MEDIA COVERAGE