Patient stories are powerful - Our friend @AutumnAustin616 shares her #lupus journey. We are all so proud of you, Autumn & cheering you on! 📣💜

#LADAorg is appreciative of our strong partnerships with our patient advocacy colleagues at the #Lupus Community Booth #2121 at #ACR25. Kudos to all of you for collaborating to improve lives!

We are excited to attend #ACR25 to network, learn and share our resources. Visit us at the Lupus Community Booth # 2121. #PatientVoice #LADAorg @Lupus_Chat @LupusMI @C_O_L_N @LupusIL @LupusNE @US_Pain @IAFaccess

Thank you to everyone who attended and supported the Metro Detroit Walk for Lupus! Over 300 attendees came together to bring visibility to an often invisible illness. We extend a heartfelt thank you to all participants, volunteers, generous donors and event sponsors for making

Thank you for sharing this personal story about the Grand Rapids Walk for Lupus, @grmagazine! https://t.co/3vS8fOX0e6

Thanks, @WGVURadio! Michigan Lupus Foundation launches a comic book to fund lifesaving work.

The Michigan Lupus Foundation has been growing! Thank you for helping us reach more #lupus warriors across the state of #Michigan and beyond. Together we can help raise awareness and build a supportive community for those living with this incurable, debilitating and often

Thank you for ending #LupusAwarenessMonth with us by making our Lansing Walk for Lupus a success! We extend a heartfelt thank you to all participants, volunteers, supporters and our generous event sponsors. By coming together, we not only raised critical awareness of #lupus but

People with #lupus can experience cognitive symptoms such as having a hard time thinking clearly or remembering things. This is called #brainfog. Brain fog can impact cognitive skills like language, memory, coordination, mood and vision. #LupusAwarenessMonth

Thank you @wilxTV for helping to spread lupus awareness during #LupusAwarenessMonth! https://t.co/qVza6R6R5N

Many people living with #lupus struggle to maintain full-time employment. A national statistic estimates only 30% of lupus patients are able to be employed full time. If you have lupus and are able to continue working, the Americans with Disabilities Act allows you to ask your

People living with #lupus are often told they do not look sick since they display no noticeable signs of the illness. While it can be taken as a compliment, it also takes away how hard each person with lupus fights every single day. Not all disabilities or illnesses are visible.

The majority of those with #lupus identify #fatigue as their primary symptoms. Lupus fatigue is not the same as feeling tired — it's a tired sleep can't fix. #lupusawareness #lupusawarenessmonth

Happy #worldlupusday!! Thank you to everyone who gathered in Traverse City and Livonia to spread awareness! World Lupus Day is sponsored by the World Lupus Federation, a coalition of #lupus patient organizations from around the world, united to improve the quality of life for

The Michigan Lupus Foundation is pleased to announce @GovWhitmer officially proclaimed May 2025 as #LupusAwarenessMonth in the state of Michigan. We thank Governor Whitmer for this important recognition! 💜 https://t.co/iRqaBuLhSd

While the exact cause of #lupus is unknown, research shows it’s a combination of genetic, hormonal and environmental factors. People with an inherited predisposition for #autoimmune may develop the disease when they come into contact with something in their environment that

Only five treatments are currently approved for #lupus (aspirin, corticosteroids, hydroxychloroquine, belimumab, and anifrolumab-fnia) and two drugs for #lupusnephritis (belimumab and voclosporin). But there are many in the pipeline, hope is on the horizon! #LupusAwarenessMonth

#Lupus is a chronic autoimmune disease with a wide range of symptoms, which can vary greatly between individuals.

What is #lupus? 💜 #lupusawareness #lupusawarenessmonth #lupuswarrior #milupus #chronicillness #autoimmune #michiganlupus #makelupusvisible