The Beginning
LupiesUnite is a non-profit organization founded in 2019 to address the lack of awareness surrounding Lupus and other autoimmune illnesses. Lupus, a chronic autoimmune disease, causes inflammation throughout the body, resulting in symptoms such as fatigue, joint pain, rashes, and organ damage. Unfortunately, Lupus is often misdiagnosed, and the lack of awareness about the disease in the medical community and the world has led to inadequate research funding, limited treatment options, and delayed diagnosis. According to the Lupus Foundation of America, 1.5 million Americans and 5 million people worldwide are affected by some form of Lupus. Lupus is known to affect 90% of women and is 2 to 3 times more prevalent in ethnic communities. Only 10% of men are diagnosed with Lupus. LupiesUnite aims to educate and increase awareness about Lupus and other underlying autoimmune illnesses, such as Fibromyalgia and Rheumatoid Arthritis.
Our organization provides various programs and services to offer you the knowledge you need on anything related to Lupus. We provide patient testimonials, mentor services for Lupus patients and their loved ones, and much more. Our mentor services pair newly diagnosed Lupus patients with more experienced Lupus patients to provide them with guidance, support, and information. Our organization also offers educational workshops, support groups, and community events to raise awareness about Lupus. We believe everyone deserves access to accurate information about Lupus, and our mission is to provide resources and support to those affected by the disease.
We are committed to advocating for research funding and spreading awareness about Lupus to improve diagnosis, treatment, and quality of life for those living with Lupus. LupiesUnite welcomes donations of all kinds to support those with Lupus who require assistance with medication, clothing/shoes, and school supplies. Our mission is to raise awareness about the severity of Lupus and the damage it can cause, while also showing that those living with the condition can still achieve their dreams and goals. Lupus is no longer the death sentence it once was, and with proper medical care and a personalized treatment plan, individuals with Lupus can lead fulfilling lives. We want the world to know about Lupus in the same way that Cancer, Diabetes, and AIDS are widely recognized, and our ultimate goal is to give Lupus the recognition it deserves, particularly in the medical community
BOARD OF DIRECTORS
Janay Townes- Founder/CEO
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