Rivka Solomon is a writer and patient advocate for myalgic encephalomyelitis (ME). She resides in Massachusetts. In 1990, while studying international relations at graduate school, Solomon became ill with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and has remained ill since. Her advocacy work includes coordinating protests and writing articles about ME/CFS.
Articles, talks & interviews[edit | edit source]
- 2011, Ms Magazine - Rivka Solomon Acts Up, Chronic Fatigue Be Damned
- 2015, San Francisco Chronicle - Chronic fatigue syndrome recognized at last by Rivka Solomon
- 2016, Rivka Solomon speaks at #MillionsMissing protest in San Francisco.
- 2016, Why we shouldn’t call it ‘chronic fatigue syndrome’ by Rivka Solomon
- 2017, Rivka asks Senator Markey at Town Hall for NIH Funding
- 10 May 2017, "This Mother’s Day, We’re Fighting For Women’s Health Equality" in Ms. Magazine Blog
- 16 May 2019, Ronald G. Tompkins, MD, ScD, has a candid conversation with patient and advocate, Rivka Solomon - (Video)
Online presence[edit | edit source]
See also[edit | edit source]
Learn more[edit | edit source]
References[edit | edit source]
- "Rivka Solomon Acts Up, Chronic Fatigue Be Damned – Ms. Magazine". msmagazine.com. Retrieved Sep 10, 2019.