Mary Ann Kindel: Difference between revisions
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
(added cat) |
(typo) |
||
| Line 15: | Line 15: | ||
</references> | </references> | ||
[[Category:People with ME, CFS, and/or FMS]] [[Category:Advocates or allies]]Category:American advocates or allies | [[Category:People with ME, CFS, and/or FMS]] [[Category:Advocates or allies]][[Category:American advocates or allies]] | ||
Revision as of 04:54, April 12, 2017
Mary Ann Kindel is a patient advocate who lives with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). She launched the not-for-profit ME Advocacy in 2014. She is part of the advisory committee and has contributed to the ME Advocacy blog.[1]
Talks & interviews
- 2015, "Low awareness often makes chronic fatigue syndrome diagnosis difficult" by Kyla Woods, WLWT News 5
Online presence
Learn more
See also
References
- ↑ http://www.meadvocacy.org/about ME Advocacy: About
