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Welcome | Indiana

No One Fights Alone in Indiana

Over 36,000 Hoosiers are living with lupus. Whether you are living with lupus or loving someone with lupus, we are here.

This is my chapter   |   
We hope to see you in 2022!
Download 2022 Chapter Timeline of Events

Welcome Brian Rothenberger

Please join our Board of Directors and staff in welcoming Brian Rothenberger as our new CEO! We’re excited to have Brian as part of our team and are confident his non-profit experience as well as his extensive history of successful leadership and relationship development, productivity and quality improvement, and strategic support will help ensure our Chapter is able to live our mission of improving the quality of life for all people affected by lupus through research, education, support and advocacy.

Learn More About Brian
Faces of Lupus Fashion Show

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.

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An image of the dome of the US Capitol building against a blue sky with a stamp that reads "Turn Capitol Hill purple"

We hope you'll join us on June 26-28 for the virtual National Lupus Advocacy Summit.

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LFA, Indiana Part-Time Development Associate Job Opportunity

Are you a mature, confident, organized, detail-oriented individual who is looking for a new challenge? Would you like to join a small but dynamic group of mission-driven people who want to make a difference in the lives of those living with lupus? If so, we would like to speak with you! Please send resume to

Director of Operations and Patient Services Job Description
In the Loop logo

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!

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The Patient Navigation Program is designed to help patients overcome barriers to healthcare.

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!

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Coronavirus image

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.

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Make Your Mark logo

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.

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6 Years

On average, it takes nearly six years for people with lupus to be diagnosed, from the time they first notice their lupus symptoms.

1.5 Million Americans

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.

Community Partners

We are very thankful to our Chapter's 2022 Community Partners!

Partnership Sponsors

  Lilly logo     GSK Us In Lupus logo

Guardian Sponsor



Join the Fight

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.

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