Solve M.E. Spearheads the First Nationwide Long Covid PSA campaign
We are excited to announce a new program being introduced by Solve M.E. and invite our community play an important part in its roll out. Solve M.E. is on the […]
World ME Alliance Members “Do Not Endorse the Lightning Process”
This article was first published by our friends at the World ME Alliance. Read it here. The World ME Alliance and its members have worked closely over the past few […]
CureME’s Caroline Kingdon on Representing People with Severe ME in Research
Caroline Kingdon, RN, MSc, is a research nurse for CureME, an organization at the forefront of participatory epidemiological, clinical and laboratory research into ME/CFS in the UK. She is also […]
Solve M.E. Board Member Testifies at Congressional Hearing
House Holds Hearing on “Understanding and Addressing Long Covid” This week, the Select Subcommittee on the Coronavirus Crisis held a hearing on understanding and addressing Long Covid and its consequences. […]
Guest Feature from Fiona Lowenstein: Chronic Illness Communities on Vaccines
The following essay is a guest feature from our friend, journalist Fiona Lowenstein. Fiona is the founder of Body Politic, a grassroots health justice organization for individuals with Long Covid. In […]
CDMRP Program at Department of Defense Announces $1.6M Grant for ME/CFS Research
At Solve M.E., our advocacy team is dedicated to opening new funding avenues for ME/CFS, Long Covid, and post-infection disease research and care. We’re excited to share that our efforts […]
Tracking of ME/CFS Cases in the Revised US ICD-10-CM
Since 2015, the 1-2.5 million Americans with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) have been effectively nonexistent, at least as far as US disease tracking systems are concerned. Americans don’t experience […]
Long Haul Voices Episode Two Available Worldwide!
The second episode of our three-part video series, Long Haul Voices, is available to view online now! In this episode, we highlight the voices of prominent medical professionals, scientists, and […]
Solve M.E. Research Team at IACFS/ME 2022 Conference
Join Solve M.E.’s research team at this year’s IACFS/ME for a special presentation by Solve M.E.’s Kate Mudie, as well as a poster session, during the 2022 Virtual Scientific Conference […]
Is There a Herpesviruses-Related Antibody Signature In Patients With ME/CFS?
Many patients with ME/CFS experience common herpesviruses infections at their disease onset. Alternatively, others experience reactivation of the same infections during the disease course. These facts suggest the existence of […]
New Hope for Diagnosing and Treating Post-Infection Illnesses: Lessons Learned from HIV/AIDS
In this special webinar, Dr. Steven Deeks (Professor of Medicine-in-Residence at the University of California, San Francisco) will be hosted by Solve M.E. Medical Advisor Dr. David Hardy (former Director […]
2022 INIM Conference
Join the Institute for Neuro-Immune Medicine (Nova Southeastern University) on Friday, June 10th for their annual 2022 INIM Conference. The Institute’s clinicians and researchers will discuss research and the various […]
