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ME/CFS SOUTH AUSTRALIA INC

Registered Charity 3104

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sacfs@sacfs.asn.au

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ME/CFS South Australia Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.

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CDMRP Funding Announcement Comes Just 24 Days After Congress Opens Potential $350 Million To ME/CFS Researchers

Sunday 19 January 2020

 

From Solve ME/CFS (via email):

 

Solve ME/CFS Initiative
 

CDMRP Funding Announcement Comes Just 24 Days After Congress Opens Potential $350 Million to ME/CFS Researchers

Saturday January 18, 2020

ME/CFS researchers can compete for 5 new funding streams and over 100 awards, up to $7.2 million per award

As we announced earlier this week, the two-year effort by Solve M.E. to add ME/CFS as an eligible topic area for the Peer Reviewed Medical Research Program (PRMRP) is a success!

This program will receive $350 million in 2020 and ME/CFS will compete with 43 other diseases for over 100 grants in 5 program areas. These areas are:

  • Clinical Trial Award
  • Discovery Award
  • Focused Program Award
  • Investigator-Initiated Research Award
  • Technology/Therapeutic Development Award

Now, just 24 days after the signing of the FY20 Defense Appropriations Act that designated ME/CFS as a Congressionally Directed Topic Area and eligible for funding, grant award pre-announcements have been released!

Last year, the program funded 107 awards! Read more about the PRMRP funding opportunities here. Please share this news far and wide with other community members, academics and scientists, particularly those who might apply for the potential $350 million in research funding.

Let’s bring home the dollars for ME/CFS research!

 

Full article…

 


 

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