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
July 13, 2022
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
The second episode of our three-part video series, Long Haul Voices, is available to view
Today, AIM ImmunoTech, an immuno-pharma company focused on the research and development of therapeutics to
https://www.youtube.com/watch?v=W_UFlzaNU6g&list=PLbO5abv0daLXDapXhiaVgeDJaIU66DRDA&index=1 New and timely series will amplify the experiences of individuals with Long Covid and
On May 12th each year, we focus a day on learning about, raising awareness of,
DePaul Univeristy Professor of Psychology Leonard Jason, PhD and Solve M.E. President and CEO Oved