Black women have long been ignored in the CHRONIC ILLNESS community.
We Are Ill is changing the narrative of MS, LUPUS AND OTHER AUTOIMMUNE DISEASES, and improving the overall health outcomes of Black women.
Mission & Vision
Too often, Black women living with multiple sclerosis (MS), lupus and other autoimmune diseases are rendered invisible in a system that overlooks their symptoms, dismisses their pain, and excludes them from life-saving information and support. Though highly educated, and accomplished, many find themselves misdiagnosed, underrepresented in medical research, and alone in navigating the complexities of chronic illness.
We Are ILL is the soft place to land. We exist to rewrite the narrative for Black women with MS, lupus and other autoimmune diseases. Our programs provide transformative community, elevate patient education, and build confidence to self-advocate in both clinical and everyday settings. Whether newly diagnosed or years into their journey, our community helps women go from surviving to thriving — physically, emotionally, and socially.
We’re not just offering resources. We’re building a movement. Because when a woman feels informed, supported, and connected, she becomes a leader in her own care and a force in her community. We're redefining what "sick" looks like.
Our Mission
We Are ILL empowers Black women living with MS, lupus and other autoimmune diseases by providing culturally relevant education, community, and advocacy that transforms isolation into belonging and equips women to thrive with strength, dignity, and support.
Our Vision
A world where every Black woman living with MS and lupus is seen, heard, supported, and thriving — equipped with the tools, knowledge, and sisterhood needed to boldly navigate her MS or lupus journey.