Donna Pearson

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Donna M. Pearson is a patient advocate from Holland, Massachusetts. She became ill with myalgic encephalomyelitis (ME) in 2003 following a flu, that in her words, "was far worse than anything I had ever experienced." Prior to becoming ill she worked as the Vice President for a real estate syndication firm, established her own management company, raised a family, and led a full and active life.[1]

Massachusetts CFIDS/ME & FM Association[edit]

Pearson is an officer of the Massachusetts CFIDS/ME & FM Association, a large and respected patient advocacy group.[2]

Chronic Fatigue Syndrome Advisory Committee[edit]

Pearson serves as a voting member of the HHS's Chronic Fatigue Syndrome Advisory Committee (CFSAC) for the term: 06/16/14 to 06/16/18 and chairs the IOM/P2P Working Group for CFSAC.[3]

Questions to NIH during Advocacy Call[edit]

Talks & Interviews[edit]

References[edit]

  1. http://www.hhs.gov/advcomcfs/meetings/presentations/pearson_donna_100312.pdf
  2. https://www.masscfids.org/newsletters/542-2014-06-june-summer-has-finally-come-to-new-england
  3. http://www.hhs.gov/advcomcfs/meetings/agendas/cfsac20160517-agenda.html
  4. https://www.nih.gov/nih-me/cfs-advocacy-call-0


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