Accelerating Severe ME/CFS Research

August is Severe ME/CFS Awareness Month–a time to reflect on the toll this disease takes on those suffering from severe ME/CFS symptoms and advocate for better research, support, and treatment. […]

Hope Amid Uncertainty

A special message from Solve M.E. President and CEO Emily Taylor With so much speculation about the future, it’s easy to feel unsettled – and uncertainty is especially hard for […]

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