by Stephanie Holmes | Mar 18, 2021 | Lupus Foundation of America
Yesterday, the Lupus Foundation of America participated in a virtual briefing with Congress to share the unique impacts of the COVID-19 pandemic on people with lupus. This briefing was held by the Protecting Immunocompromised Collaborative which is led by the Immune...
by Stephanie Holmes | Mar 12, 2021 | Lupus Foundation of America
Last week, over 3,700 lupus advocates from all 50 states and 76 countries across the globe registered for the Lupus Foundation of America’s Digital Lupus Advocacy Summit. The successful event featured several engaging panel discussions, bringing the latest lupus news...
by Stephanie Holmes | Mar 11, 2021 | Lupus Foundation of America
In celebration of Women’s History Month, we want to spotlight a few remarkable women that are making an impact and inspiring those in the lupus community in every possible way. Below, we’ve highlighted the stories and accomplishments of some of these phenomenal...
by Stephanie Holmes | Feb 22, 2021 | Lupus Foundation of America
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by Stephanie Holmes | Feb 11, 2021 | Lupus Foundation of America, Research News
In addition to reducing lupus flare risk and frequency, the drug Benlysta® can also minimize healthcare costs, according to a new study. Benlysta is a prescription medication to treat lupus and lupus nephritis (LN) administered intravenously (IV) or as an injection...
by Stephanie Holmes | Feb 9, 2021 | Lupus Foundation of America
The Sharing the Journey series is by you and for you. In your own words, we highlight the perspectives and personal experiences of people who struggle with lupus each day. This month, we asked Sharing the Journey participants the following question:Alopecia (hair...
