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Dedicated to increasing awareness about
systemic lupus erythematosus (SLE), disease activity and related organ damage

SLE Resources for Patients and Caregivers

The need for healthcare providers to effectively engage with patients with SLE is ongoing and the stakes are high. Even when patients have no complaints and no visual signs of disease, organ damage can be occurring. We've developed these tools to help both you and your patients communicate and be vigilant.

Patient Leaflet Builder

Healthcare Team and Treatments Worksheet

The Lupus Checklist

Lupus Action Plan

Lupus Impact Tracker

How Lupus Affects Your Body

How to Manage Stress

Lupus: Just the Facts

Living with Lupus

Us in Lupus

My Lupus Log

The Lupus Impact Tracker is a trademark of Rush University Medical Center and the Board of Trustees of the University of Illinois.

Other Resources

We encourage you to visit these nonprofit agencies working to raise awareness, improve diagnosis and treatment, and provide support to those living with lupus.

Lupus Research Alliance

The world's largest private funder of lupus research, the Alliance aims to find better treatments and ultimately prevent and cure systemic lupus by supporting bio-medical research. Find Out More

National Resource Center on Lupus

More than 600 medically-reviewed multimedia resources on lupus are available in English and Spanish, including research updates, informational articles, and Q&As.
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The Lupus Initiative

A national program of the American College of Rheumatology (ACR), the Initiative is dedicated to reducing health disparities in lupus. It offers resources in English, Spanish, Chinese, Arabic, and other languages. Find Out More