Saturday, April 16, 2016

Lyme's Secret Patients

.
(Don't miss other blog posts! Click "BLOG" in the header above!)



The following is a copy of an email I received from  www.LymeDisease.org.

You can read it here and click the links here.



Lyme Disease.Org Logo
IDSA won't release names of "patient representatives" on Lyme panel. What are they hiding?

Last year, LymeDisease.org joined with other groups in protesting that the IDSA's "Lyme patient representative" didn't have Lyme or know anything about it. 

In response, the IDSA now says it has appointed four more patient representatives, but they won't tell anybody who they are. READ MORE.



IDSA says new guidelines process will take 2-5 years. Why does CDC still endorse the old ones?

Although IDSA's Lyme guidelines have been removed from the National Guidelines Clearinghouse for being out-dated, the CDC continues to endorse them. READ MORE.


Ask your senators to co-sponsor Lyme bill, S. 1503


The Lyme and Tick-Borne Disease Prevention, Education, and Research Act of 2015 is still in committee. Please use our Voter Voice system to contact your senators, asking them to co-sponsor this important legislation. Details here.

LymeDisease.org, publisher of The Lyme Times, is the Lyme community's leading source of news, information, and health policy analysis. 
     
Like us on Facebook   Follow us on Twitter   View our videos on YouTube  View our profile on LinkedIn

Copyright © 2016. All Rights Reserved.

No comments:

Post a Comment

Thanks for taking the time to read and comment!