WHAT WE DO

Aboutus - About us

• DISSEMINATE ME/CFS and FM literature to medical and legal professionals and the general public;

• INTERVENE in court cases of benefit to the ME/CFS and FM population;

• COLLABORATE with support Networks in both Canada, U.S. and elsewhere;

• REPRESENT the ME/CFS and FM population at meetings with government officials and politicians;

• PUBLISH a quarterly newsletter QUEST to keep the ME/CFS and FM population informed;

• PROVIDE resource materials for disability issues;

• KEEP ABREAST of research on ME/CFS and FM around the world;

• SUPPORT scientific endeavors;

• EDUCATE the school systems on youth with ME/CFS and FM;

• KEEP a roster of Lawyers who are experienced in ME/CFS and FM issues;

• LIAISE with all forms of media on ME/CFS and FM issues;

• WORK with Networks of related diseases;

• DO Special Projects that develop;

• HOLD conferences on ME/CFS and FM;

• ACCEPT opportunities to work with doctors, researchers and legal professionals;

• INFORM people who contact us on ME/CFS and FM;

• REFER people to the best help available;

• FOLLOW-UP leads on ME/CFS and FM to its source;

• USE website, Facebook and Twitter;

• SEND announcements to those on our email roster;

ADMINISTER the Dr. Alison Bested Scholarship Fund; and

• DEAL with issues as they arise.

FOR DETAILS ON THE ABOVE, PLEASE VIEW THE HISTORY & ACHIEVEMENTS OF THE NATIONAL ME/FM ACTION NETWORK.

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