Gabby Klein

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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]

Talks and interviews[edit | edit source]

HHS/CFSAC Testimony[edit | edit source]

Online presence[edit | edit source]

  • Gabby Klein is on Twitter.
  • Facebook
  • Website/Blog
  • YouTube

See also[edit | edit source]

Learn more[edit | edit source]

  • Wikipedia

References[edit | edit source]

  1. ↑ https://thoughtsaboutme.files.wordpress.com/2013/11/sebelius_letter_advocates_updated.pdf
  2. ↑ https://wayback.archive-it.org/3919/20140324193134/http://www.hhs.gov/advcomcfs/meetings/presentations/gabby-klein.pdf.pdf

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.

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