Sam Carter

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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 (Jun 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 Jan 29, 2019. 
  3. Carter, Sam (Feb 15, 2016). "Exploring changes to PACE trial outcome measures using anonymised data from the FINE trial". PubMed Commons. Archived from the original on Feb 2016. 


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