The Lupus Foundation of America has unveiled the National Resource Center on Lupus. This new website is a one-stop resource for all things lupus. The Resource Center aims to connect, empower and educate those whose lives are impacted by this devastating and unpredictable disease by providing trustworthy, reliable and high-quality resources, programs and emotional support services. The Lupus Foundation of America estimates that 1.5 million Americans, and at least five million people worldwide, have a form of lupus.
“The National Resource Center on Lupus was a vision that started a decade ago to bring together in one place the best resources and information available on lupus,” said Sandra C. Raymond, Lupus Foundation of America President and CEO. “The content available on the National Resource Center on Lupus is based on forty years of experience and insights that we have gathered working closely with world-renowned lupus experts and the lupus community, as well as from a comprehensive research effort conducted by the organization.”
The results from the Lupus Foundation of America’s National Needs Assessment on Lupus, conducted last year, took a broad, yet deep look at the very specific needs and wants of the diverse lupus patient, caregiver and health care professional communities. Based on this input, the Lupus Foundation of America developed more than 600 medically-reviewed resources in English and Spanish about all aspects of lupus. New content will be added on a regular basis and will be developed in response to the needs identified.
Visitors can easily find what they are looking for by:
“The Resource Center provides a comprehensive and ever-growing repository of medically-reviewed content provided in a variety of formats that physicians can feel confident sharing with patients and their families.”
The Resource Center provides support to people who might have lupus, people who are newly-diagnosed or people living with lupus.
Examples of resources available include:
Source: Lupus Foundation of America