by Stephanie Holmes | Sep 14, 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:At times, opening...
by Stephanie Holmes | Aug 25, 2021 | Lupus Foundation of America
Register NowJoin us for our next virtual Lupus & You: Answers. Advocacy. Action. event. Hear from lupus experts on how lupus affects the skin, disease management and education, and learn how you can engage in advocacy and awareness in your...
by Stephanie Holmes | Aug 19, 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:What key questions...
by Stephanie Holmes | Aug 2, 2021 | Lupus Foundation of America
This type I interferon receptor antagonist demonstrated early and sustained benefits for people with moderate to severe systemic lupus erythematosus.The U.S. Food and Drug Administration (FDA) has approved Saphnelo™ (anifrolumab-fnia) as a treatment for adults...
by | Aug 2, 2021 | Lupus Foundation of America
This type I interferon receptor antagonist demonstrated early and sustained benefits for people with moderate to severe systemic lupus erythematosus.The U.S. Food and Drug Administration (FDA) has approved Saphnelo™ (anifrolumab-fnia) as a treatment for adults with...
by Stephanie Holmes | Jul 26, 2021 | Lupus Foundation of America
I was 15 years old when I was diagnosed with lupus, I was so sick; I remember my mom taking me to the doctor in a wheelchair, sitting me in front of the receptionist desk and begging for help. I recall making countless visits to our family doctor where I never got any...
