Save the date of Saturday, July 23rd, for the Faces of Lupus Fashion Show Gala! This fun fundraiser features 30 beautiful and handsome models, all of whom have lupus or are a healthcare provider to people with lupus.Learn More
Our current CEO La Toija Snodgrass will be moving out of state with her family so we are looking for an energetic, experienced nonprofit professional to serve as our Chief Executive Officer. If interested, please send cover letter and resume to Board Chair Robin Miner at email@example.com.CEO Job Description
Congratulations to Destney Johnson on being the recipient of the Marlene Stepanek Lupus Legacy Scholarship!Learn More
If you weren't able to attend the In the Loop - Healthy Living with Lupus symposium, a few of the presentations from the symposium are available!Learn More
We'd love to learn and share how our Chapter has impacted your life or a family member's life. Please send your stories (250 words or less) and a photo headshot and we'll share in our eNewsletter, website and social media. Send story to Damiah at firstname.lastname@example.org.Read Stories
Looking for someone who can provide support and assistance to overcome the barriers that come along with lupus? That’s what our patient navigators do!Learn More
We hope you'll join us on June 26-28 for the virtual National Lupus Advocacy Summit.Learn More
Everything you need to know in one place. Stay updated on all the latest COVID-19 news as it impacts those with lupus from resources, news, and programming. We will be keeping you updated and provide virtual programming to get you through these unprecedented times. You are not alone.Learn More
Make Your Mark is the community fundraising program of the Lupus Foundation of America. Each year, hundreds of Make Your Mark members organize unique events and athletic feats that raise money to fight lupus. Use your passion to raise funds for lupus through a local event, special occasion, athletic competition or whatever you have in mind.More Information
On average, it takes nearly six years for people with lupus to be diagnosed, from the time they first notice their lupus symptoms.
The Lupus Foundation of America estimates that 1.5 million Americans, and at least five million people worldwide, have a form of lupus.
Lupus strikes mostly women of childbearing age. However, men, children, and teenagers develop lupus, too. Most people with lupus develop the disease between the ages of 15-44.
We are very thankful to our Chapter's 2022 Community Partners!
The Lupus Foundation of America, Indiana Chapter is part of a national force devoted to solving the cruel mystery of lupus while providing caring support to those who suffer from its brutal impact. If you join the fight, we will not have to concede victory to this terrible disease. With your support and involvement, we will be able to solve the cruel mystery of lupus in our lifetime and end its devastating impact on millions of lives.Donate Now