Healthcare Provider Resources | Southeast
Your Partner in Lupus Patient Care
As a trusted healthcare provider, you play a vital role in the lives of individuals with lupus. We are committed to supporting physicians like you in your efforts to provide the best possible care for people with lupus. We've compiled a comprehensive list of resources designed to support you and your office. Here, you'll find patient-centered tools, resources, and ways in which we can support those living with lupus and their families. There are also opportunities for collaboration and for LFA to support your work through grants, all aimed at improving outcomes for your patients.
One of the top requested resources is a list of lupus-aware physicians. Take a moment to add your practice to our list or make sure your information is up-to-date. Share with others who should be on this list.
LFA supports lupus research in areas where there are gaps in scientific knowledge or in areas that have not received adequate funding. Learn more about how we can support your important work.
Lupus Science & Medicine® is a peer-reviewed, open access, online journal that provides a central point for publication of basic, clinical, translational, and epidemiological studies of all aspects of lupus and related diseases.
The SELF app is a free self-care program designed to help people with lupus live their best lives. SELF can be your patients coach to help them manage lupus, symptoms, manage stress, manage medications and work with their healthcare team. It’s convenient and customized--offering easy-to-use tools, trackers, skill-building activities, support, and reminders.
Encourage your patients to join our lupus support groups in-person or online, led by LFA-trained facilitators who provide a welcoming and supportive space. We are here for your patients every step of the way. Whether they prefer connecting face-to-face or from the comfort of their own home, we have a supportive community waiting to welcome everyone.
LFA conferences connect and support lupus warriors and caregivers with the latest advances, valuable resources, and a build strong community. We would love to see your patients at a conference near you. Additionally, if you are interested in participating as a speaker, please email infose@lupus.org.
The Lupus Foundation of America's health education specialists can help your patients find trustworthy information and resources to support them in their journey, find community and better cope with their diagnosis.
This is the largest living collection of up-to-date resources and information on lupus providing patients with the information they need from caregiver support to nutrition to understanding lab results and more!
The Lupus Foundation of America hosts Walk to End Lupus Now events every year across the nation. You can take part through sponsorship and community engagement. Your partnership will be an impactful collaboration to enhance patient care and empower patients.
Download the form here.
Sponsor a walker at the Walk to End Lupus Now event to support medical research, patient care, and essential services. Your contribution helps advance treatments and improve outcomes for those with lupus. Together, we can bring hope and make a difference in their lives.
Download the form here.
We invite your practice to start a team and continue to lead the way!