- Connect with LRI:



- YouTube
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Tell Congress in 2010!
The Lupus Research Institute’s National Coalition is the Patients’ Voice for Lupus Research
Add your voice! Tell Congress to:
- increase government research funding
- support federal programs for eliminating racial disparities in access to good care and treatment
- increase access to care nationwide
- vote for effective health insurance reform!
Ours was the first lupus advocacy day of 2010: March 4th in Washington, D.C. Read about it
Our 2010 Advocacy Day is past, but we need your voice for lupus throughout the year! Sign up for e-alerts that include information on advocacy victories and the date for Tell Congress 2011!
Via email:
Senators: http://www.senate.gov/general/contact_information/senators_cfm.cfm
U.S. Representatives: https://writerep.house.gov/writerep/welcome.shtml
Via Twitter:
Use http://tweetcongress.org/ to find your congresspersons on Twitter.
A Patient’s Voice in Lupus Research
“I was thrilled to share my experiences and concerns with the esteemed panel with which I worked, and humbled to hear from several reviewers that my insights made a tangible and positive difference.” More »





















