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Legislative Successes

A legacy of legislative success

Since 1977, the Lupus Foundation of America has been driving effective policy change at the federal and state level to improve the lives of people with lupus. We’ve succeeded in the past, and with the continued support of our advocates, we’ll succeed in the future.

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Our Approach to Advocacy

When it comes to improving the lives of people living with lupus, there is no issue too small or too daunting for the Lupus Foundation of America. The government is one of our most valuable partners in the fight against lupus, and we’ll never stop leveraging their resources and pushing them to be more responsive to the needs of the lupus community. We know that no one can tell the lupus story better than our network of advocates, so our goal is to provide advocates with opportunities to engage with their elected officials and maximize the impact by amplifying their voices.

Lupus Awareness Month 2022 – Government Proclamations

During Lupus Awareness Month in 2022, the Foundation and its advocates saw tremendous success in obtaining government proclamations to draw further attention to Lupus Awareness Month among both elected officials and the general public.


Lupus Awareness Month proclamations were obtained by our Southern California region and its advocates in the following locales:

  • City of Costa Mesa
  • City of Glendale
  • City of Santa Monica


Lupus Awareness Month proclamations were obtained by our Florida region and its advocates in the following locales:

  • City of Belleair
  • City of Dunedin
  • City of Kissimmee
  • City of Oldsmar
  • City of Orlando

New York

In New York City, our Northeast Region and its Advocacy Chair, Olga Lucia Torres, obtained a commemorative message from Mayor Eric Adams recognizing Lupus Awareness Month and sharing his best wishes for an "effective and successful Awareness Month."


In Washington, our Pacific Northwest Region and its Advocacy Chairs, Erin Elsasser and Sanjay Mishra, obtained a proclamation from Governor Jay Inslee recognizing May as Lupus Awareness Month.

Photo of unused microscope in a research lab

The National Institutes of Health (NIH) have committed more than $615 million to lupus research in the last 5 years alone, making them by far the largest public funder of lupus research in the world. Each year, we urge Congress to support robust funding for NIH, allowing them to conduct basic, clinical, and translational research that will lead to the identification of new targets for lupus drug development.

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LFA CEO Steve Gibson has a converastion with President George W. Bush
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The MAPRx Coalition

We founded the Medicare Access for Patients Rx (MAPRx) Coalition in 2005 to strengthen and improve Medicare Part D. For more than 44 million Americans over the age of 65 or living with a chronic disease, Part D provides timely, affordable access to prescription medications. Today, MAPRx has become the preeminent Part D coalition with more than 60 member organizations representing patients, caregivers, and healthcare professionals.

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More Federal Lupus Initiatives

Lupus Federal Working Group

The National Institutes of Health brings together federal agencies with an interest in lupus to better coordinate their efforts. Learn more.

Lupus Public Health Agenda

The CDC’s Agenda provides a broad public health approach to lupus diagnosis, disease management, treatment, and research. Learn more.

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