Gabby Klein
Gabby Klein is a contributor to the ME Advocacy blog. She was a Vice President of Administration for an insurance company[1] before she became ill with myalgic encephalomyelitis (ME) in February 2003 after a stomach flu.[2]
Contents
Talks and interviews[edit | edit source]
HHS/CFSAC Testimony[edit | edit source]
- May 2011, Written testimony CFSAC Meeting
- May 2013, Public Testimony CFSAC Meeting
- December 2013, Public Testimony CFSAC Meeting
- January 2015, Public Testimony CFSAC Meeting
- Jan 13, 2017, Public Testimony CFSAC Meeting
Online presence[edit | edit source]
- Gabby Klein is on Twitter.
- Website/Blog
- YouTube
See also[edit | edit source]
Learn more[edit | edit source]
- Wikipedia
References[edit | edit source]
Chronic Fatigue Syndrome Advisory Committee (CFSAC) - (sometimes pronounced SIF-SACK) A US government advisory council that met twice per year, covering current topics related to Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. Meetings usually lasted for two days and the results were presented to the Secretary of Health and Human Services (HHS). After 15 years, on September 5, 2018, CFSAC's charter was not renewed by the Department of HHS, effectively dissolving the committee without notice or warning.
The information provided at this site is not intended to diagnose or treat any illness.
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history.
