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Hello from the Solve ME/CFS Initiative. We want to share our latest news and research with you, but we also want to respect your space and not spam the forums. In order to do that, we are starting a monthly thread where will we add all of the latest news from SMCI. Throughout the month we plan...

SMCI supports worthy ME/CFS research projects across a range of disciplines. In 2017, we funded five research projects and their work is currently underway. The 2017 Ramsay study from Drs. Jonas Blomberg, Jonas Bergquist, Carl-Gerhard Gottfries, and Olof Zachrisson of Uppsala University and...

The Solve ME/CFS Initiative (SMCI) National ME/CFS Patient Registry, developed in partnership with the Genetic Alliance and Platform for Engaging Everyone Responsibly (PEER), is preparing for launch in the first half of 2018. As part of the roll-out, we will be publishing a series of articles in...

The Solve ME/CFS Initiative will be returning to Washington DC for the second annual ME/CFS Advocacy Day on Tuesday, May 15, 2018. Save the date! More details and a link to register will be available soon. ME/CFS Advocacy day is a full-day on Capitol Hill bringing people with ME/CFS and their...

As a follow to their well-received piece on ME/CFS, Ms. Magazine did a lovely profile on SMCI President Carol Head chronicling what fuels her passion: http://msmagazine.com/blog/2018/02/14/fight-follows-pain-prejudice/

ICYMI, SMCI partnered with the widely-circled women’s magazine “Ms.” and connected them with renowned author Julie Rehmeyer to produce an impactful piece on ME/CFS. The story “Pain and Prejudice” focuses on the struggle that women face in receiving a diagnosis for this devastating disease. Find...

Hello from the Solve ME/CFS Initiative. We want to share our latest news and research with you, but we also want to respect your space and not spam the forums. In order to do that, we are starting a monthly thread where will we add all of the latest news from SMCI. Throughout the month we plan...