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Are you living for lupus or living life despite lupus? Systemic lupus erythematosus (SLE or lupus) can be difficult to manage due to its unpredictable nature. As a Black woman, you’re part of the largest population affected by this condition, with a three times greater chance of having lupus as compared with white women. You’re probably also familiar with the frustration that comes from dealing with the various health disparities in the Black community.
When you combine the two—dealing with a condition that is unpredictable and inequities in healthcare—it could cause you to ask that question: Am I living for lupus—allowing it to take away precious moments—or living and enjoying life despite my lupus? If you answered that you’re living for lupus, we have some important information for you, so keep reading.
No two cases of lupus are the same—the organs it affects and the impact on daily life can be as unique as each individual. Therefore, treatment plans for lupus may vary from person to person. Oral steroids are often used to control lupus symptoms. In fact, a study has shown that Black patients with lupus are five times more likely to take chronic steroids to manage their symptoms. It is important to know that long-term use of steroids can contribute to organ damage and other potential health risks, and there are treatment options available that can help control lupus and reduce steroid use over time.
It’s up to you to look out for your health and seek the latest information about your lupus so you can talk to your doctor or healthcare provider. Even though this disease can impact you, it’s possible to still enjoy your life. One of the first steps for making this a reality is to demand more. Educate yourself, know that there may be other treatment options, and feel empowered to talk to your doctor. It’s not always easy, but feeling equipped with information through research can help you have meaningful conversations with your doctor.
When you talk to your doctor, ask about SAPHNELO® (anifrolumab-fnia) injection, for intravenous use: a first-of-its-kind treatment for your one-of-a-kind lupus. SAPHNELO is a prescription medicine used to treat adults with moderate to severe systemic lupus erythematosus (SLE or lupus) who are receiving other lupus medicines. It is not known if SAPHNELO is effective in patients with severe active lupus nephritis or central nervous system lupus. It is not known if SAPHNELO is safe and effective in patients under 18 years of age.
SAPHNELO works across different parts of the body and organs that lupus can affect. SAPHNELO has been shown to reduce lupus disease activity, which was consistent across different groups of people, regardless of race or ethnicity. SAPHNELO may also help reduce oral steroid use and lupus flares. Results may vary. Always talk to your doctor. Please see Important Safety Information below.
Please see full Prescribing Information, including Patient Information.
You may report side effects related to AstraZeneca products.
Check out our website to learn more, and ask your doctor and find out if SAPHNELO is a lupus treatment option that can work for you.
SAPHNELO is a registered trademark of the AstraZeneca group of companies.
©2023 AstraZeneca. All rights reserved. US-78531 Last Updated 11/23