Managing Lupus Symptoms Like This…
by chinyere2014
The Latest In Lupus

Love after Lupus: Tips for Keeping Romance Going in Spring
Is love after lupus possible? As in any other relationship, open communication is important. Additionally, it is important to focus on emotional and physical intimacy beyond just sex. What makes love after lupus different is that it requires that one read more about Love after Lupus: Tips for Keeping Romance Going in Spring

Living With Lupus: 9 Ways To Enhance Your Life
We’ve publicly seen the downturn that lupus can take on one’s life. From missed tour dates to multiple hospitalizations, big names like Toni Braxton, Nick Cannon, and Trick Daddy, have disclosed their complicated trials and tribulations with lupus. Bringing the read more about Living With Lupus: 9 Ways To Enhance Your Life

Ending Lupus Starts With Black Participation in Clinical Trials
As a researcher who has dedicated my career to studying lupus, I cannot overstate the critical importance of clinical trials. Lupus is a complex, multifaceted autoimmune disease that affects different patients in very different ways. By its nature, these qualities read more about Ending Lupus Starts With Black Participation in Clinical Trials

This Is What Black Lupus Patients Think About Clinical Trials
Despite being a rare disease, lupus is a leading cause of death for women under the age of 35 with Black women experiencing more severe symptoms and higher mortality rates compared to other groups. This chronic autoimmune disease causes the read more about This Is What Black Lupus Patients Think About Clinical Trials

Stronger Together: How Lupus Warriors Are Shaping the Future
The Lupus Therapeutics (LT) PALS Program: Empowering Lupus Patients Through Peer Advocacy and Clinical Trial Inclusion Lupus is a chronic autoimmune disease that disproportionately affects racial and ethnically minoritized populations, particularly Black and Hispanic women. Despite this, clinical trials for read more about Stronger Together: How Lupus Warriors Are Shaping the Future

Doctors Dismissed Her Symptoms—Then She Collapsed at a Work Conference
When Aleta was first diagnosed with lupus, she wasn’t ready to share her diagnosis with anyone beyond her closest family and friends. She wasn’t ashamed—far from it—but the idea of being treated differently made her uneasy. She didn’t want pity, read more about Doctors Dismissed Her Symptoms—Then She Collapsed at a Work Conference