The MEAction Network: Difference between revisions
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history
(→Online presence: Fix link name) |
m (+category) |
||
Line 29: | Line 29: | ||
*[http://fb.com/meactnet fb.com/meactnet] - Facebook | *[http://fb.com/meactnet fb.com/meactnet] - Facebook | ||
[[Category:Patient groups]] | |||
[[Category:American patient groups]] | |||
[[Category:Organizations]] | [[Category:Organizations]] | ||
[[Category:Blogs]] | [[Category:Blogs]] |
Revision as of 17:42, June 23, 2016
#MEAction (The Myalgic Encephalomyelitis Action Network) is an ME/CFS patient advocacy group co-founded May 12, 2015 by Jennifer Brea and Beth Mazur.
It is a global organization whose focus is on empower patients to take action to improve the research and treatment situation. #MEAction runs special interest groups focused on science & research, public education and press relations.
MEpedia was launched by MEAction.
History[edit | edit source]
Actions[edit | edit source]
PACE trial[edit | edit source]
US Congressional Outreach[edit | edit source]
Tools[edit | edit source]
Petitions[edit | edit source]
Organization[edit | edit source]
Learn more[edit | edit source]
See also[edit | edit source]
Online presence[edit | edit source]
- MEAction.net #MEActon website
- @MEActNet - Twitter
- fb.com/meactnet - Facebook