Washington University Lupus Clinic

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Thank you, Dr. Andrea Fava from Johns Hopkins Rheumatology for coming to St. Louis and presenting Rheumatology Grand Rounds to our division! We appreciate you giving several great talks while doing the St. Louis circuit! The future of in is looking bright! 💜

Today is so make sure you put on your purple! 💜💜💜

💜 is tomorrow and we’re getting ready to put on purple! Join us in raising awareness for lupus by wearing purple and showing your support. Don’t forget to tag us and use so we can reshare your posts and stories! Every photo, post, and hashtag helps make visible.

Visit our page as a guide on how to get involved and share with friends and loved ones: https://buff.ly/qHvUgoP

Thank you for highlighting our newest faculty member, Dr. Jessica Williams, WashU Med Department of Medicine! 💜

Please visit the link below to read this great summary:
Https://internalmedicine.wustl.edu/rheumatologist-and-researcher-focuses-on-lupus-care-and-rural-health/

Washington University Lupus

We had such a blast getting together at the Lupus Foundation of America, Heartland Region Walk To End Lupus Now and seeing our patients and friends! 💜

Washington University Rheumatology Division

Join our Lupus Foundation of America, Heartland Region Walk team, the WashU Wolf Pack here:

2024 Walk to End Lupus Now, St. Louis Discover your power and register for the Walk today!

The sky wanted to participate in Put On Purple day! Perfect ending to ! 💜

Washington University Rheumatology Division

Happy Put On Purple day!!! 💜 We want to see you so tag us and our friends Lupus Foundation of America - Heartland Chapter in your purple pics! 💜

Washington University Rheumatology Division

Today we celebrate lupus warriors! 💜

Today is Rare Disease Day! 🦓 As the detectives of medicine, we see quite a few patients with rare diseases. We’re proud to care for our patients that battle these diseases and today is a great day to spread awareness!

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Do you know a girl aged 12-19 living with ? Please share this post about the Heartland Chapter's Summer Jam Girls Retreat taking place June 7-9, 2024 in Branson, MO!

Get all the details here: https://www.lupus.org/heartland/summer-jam-girls-retreat-2024

Most people with lupus have skin problems like rashes or sores along with hair loss and thinning hair. Join us for this webinar as Dr. Sofia Chaudry, Associate Professor of Dermatology at Saint Louis University School of Medicine discusses the different sub-types of skin lupus and how they present, how doctors evaluate skin eruptions on people with lupus, treatment options for skin lupus and hair loss, and how to prevent skin flares.

Register to receive the login: https://www.lupus.org/heartland/lupus-the-skin-hair

Today is “Giving Tuesday” and we would love if you would join us in supporting our friends at the Lupus Foundation of America - Heartland Chapter! 💜

(Pictured here: Lupus Clinic Physicians Dr. Syed, Dr. Sen and Dr. Kim, our wonderful medical assistants Alice and Diana, and our clinical coordinator Lacey)

The Co-Pay Relief Fund is now OPEN for lupus patients with the Patient Advocate Foundation. It usually fills up quickly so please apply when you're able!

CPR Fund Now Open: Lupus

The specific eligibility criteria for the Lupus fund can be found at https://copays.org/funds . For personal assistance with the application process please contact us toll-free at 866-512-3861 or visit our application portals at https://portal.copays.org/ #/login, with access available for patients, providers, and pharmacies.

Funds – Co-Pay Relief CPR allocates funding to all patient’s that are approved for a grant so that it is available when needed by the patient. Therefore, during the period that a fund is closed to new applications, CPR continues to provide support to all patients in those funds that have an active award.