Sam Carter

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Revision as of 01:37, January 29, 2019 by Notjusttired (talk | contribs) (→‎Letters: fix typo)

Sam Carter (Samuel Carter) is an advocate and a patient with myalgic encephalomyelitis.

Talks and interviews[edit | edit source]

Letters[edit | edit source]

Online presence[edit | edit source]

  • Twitter
  • Facebook
  • Website/Blog
  • YouTube

See also[edit | edit source]

Learn more[edit | edit source]

  • Wikipedia

References[edit | edit source]

  1. Carter, Sam (June 9, 2010). "FINE Trial for CFS: Both significant and small?". BMJ. 340: c2988. doi:10.1136/bmj.c2988. ISSN 0959-8138. PMID 20534659.
  2. Carter, Sam (May 5, 2012). "A valedictory dispatch from the Psychosocial School? | Rapid Responses to articles". BMJ. Retrieved January 29, 2019. Cite has empty unknown parameter: |(empty string)= (help)
  3. Carter, Sam (February 15, 2016). "Exploring changes to PACE trial outcome measures using anonymised data from the FINE trial". PubMed Commons. Archived from the original on February 2016. Unknown parameter |dead-url= ignored (|url-status= suggested) (help)