Tina Tidmore, Coordinator of the ME/CFS World Wide Patient Alliance, advises that their January Survey indicated that  patients  want their doctors  to know about ME/CFS and thereby create a new perception of our illness.  As a result of that survey, MCWPA has developed simple instructions on how you can participate and spread the word:

Please view:  http://forum.mcwpa.org/viewtopic.php?f=61&t=183