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Tag Archives: government
Index of FDA Meeting Resources
One month to go until the FDA’s Drug Development Workshop for ME and CFS! There is a boatload of information that might be helpful to you in preparing for the meeting, even if you will only be watching online. I’ll … Continue reading
Posted in Advocacy
Tagged drugs, FDA, government, politics, speaking out, testimony, treatment
2 Comments
Two Surveys, Two Opportunities
In addition to all the ways you can participate in and comment on the upcoming FDA Drug Development for ME/CFS Workshop, you can also participate in two surveys that will collect data for presentation at the Workshop. The CFIDS Association … Continue reading
Posted in Advocacy, Research
Tagged action, CFIDS Association, DHHS, drugs, FDA, government, speaking out, survey, testimony, treatment
3 Comments
Evidence Based at NIH
Last year, NIH said it was undertaking a process to identify a research case definition for ME/CFS, but individuals like me were unable to get any additional information about what NIH intended. Now additional information has been made public in … Continue reading
Posted in Advocacy, Research
Tagged case definition, CFIDS Association, DHHS, EbMW, government, NIH, politics, recommendations, researchers, speaking out
13 Comments
Quick Announcement
Finally (!) I am able to share the news that I’ve been invited to serve on a panel at the upcoming FDA Drug Development for ME/CFS Workshop. I’ve wanted to announce this for awhile, but panelists were asked not to … Continue reading
Posted in Advocacy
Tagged action, biomarkers, DHHS, drugs, FDA, government, occupy, politics, speaking out, testimony, treatment
7 Comments
Tell It To The FDA
The much anticipated FDA meeting on drug development for ME/CFS on April 25-26th is fast approaching, and your participation is needed! There is a great deal of time set aside for patient input, but the process will work very differently … Continue reading
Posted in Advocacy
Tagged DHHS, drugs, FDA, government, living with, occupy, politics, speaking out, testimony, treatment
6 Comments
News That Is Mostly Not
This week, the CFS Advisory Committee made two announcements that I think you will want to know about. First, the spring CFSAC meeting will be May 22-23rd in Washington, DC. There is no additional information about the agenda, beyond the … Continue reading
Posted in Advocacy
Tagged CFSAC, DHHS, government, politics, recommendations, speaking out
1 Comment
Research Recommendations
See Part One – Tangled Web See Part Two – CFSAC Specific Recommendations See Part Three – Care and Services Recommendations See Part Four – Education and Training Recommendations Appropriately enough, the CSFAC has made more recommendations on research than … Continue reading
Posted in Advocacy, Research
Tagged CDC, CFSAC, DHHS, funding, government, NIH, politics, recommendations, researchers, speaking out
1 Comment
Education and Training Recommendations
See Part One – Tangled Web See Part Two – CFSAC Specific Recommendations See Part Three – Care and Services Recommendations The CFSAC lists fourteen recommendations in this category, but I covered one recommendation on ICD-10-CM in the Care & … Continue reading
Posted in Advocacy
Tagged CDC, CFSAC, DHHS, government, politics, priorities, recommendations, speaking out
Comments Off on Education and Training Recommendations
Care and Services Recommendations
See Part One – Tangled Web See Part Two – CFSAC Specific Recommendations Only ten recommendations are assigned to this category. See pages 12 – 15 of the Recommendations Chart (pdf link). Most relate to the categorization of CFS in … Continue reading
Posted in Advocacy
Tagged CFSAC, DHHS, government, politics, priorities, recommendations, speaking out
1 Comment
Showcase
The upcoming FDA Drug Development Workshop for ME/CFS will be a showcase for our disease and our patient community. We must prepare now to bring our A game on April 25th-26th. FDA first announced this workshop in the summer of … Continue reading →