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
August 9, 2022
This article was first published by our friends at the World ME Alliance. Read it
Caroline Kingdon, RN, MSc, is a research nurse for CureME, an organization at the forefront
Each year on August 8, Severe M.E. Day, we reflect on the tremendous toll this
Solve M.E. is pleased to announce that TaKeisha S. Walker recently joined us as chief
House Holds Hearing on “Understanding and Addressing Long Covid” This week, the Select Subcommittee on
The following essay is a guest feature from our friend, journalist Fiona Lowenstein. Fiona is the
Each year during Advocacy Month, we host our hallmark EmPOWER M.E. roundtable, during which patient
House Appropriations Committee Includes Specific ME/CFS & Long Covid Funding Callouts This week, the House
At Solve M.E., our advocacy team is dedicated to opening new funding avenues for ME/CFS,
Our team at Solve M.E. is excited to announce that Ilise Friedman recently joined us
As part of our efforts via the Solve Long Covid Initiative, we’ve partnered with the
Since 2015, the 1-2.5 million Americans with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) have been effectively
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