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2021 Person On the Move

Christina Carville

Christina was diagnosed with Multiple Sclerosis in 2017. Since her diagnosis, she serves as a member of the Baton Rouge Walk MS committee & was previously a member of the Baton Rouge On The Move Luncheon committee of which she was chosen to be the keynote speaker in 2019. She serves a GRAC member as well as a District Activist Leader for the National MS Society & has met with legislators both locally and on Capitol Hill in Washington D.C. to speak on behalf of people living with MS. She has also founded the Knock Out MS Foundation which is hosting their Inaugural Knock Out MS Gala in Baton Rouge this coming August.


2021 Above and Beyond Award 


Carolyn Lorio

Carolyn is a 62 year old mother of 3, grandmother of 4.  She manages a family commercial real estate business, but sneaks out on her bike early enough to catch the sunrise every chance she gets (several mornings a week).  She is working hard to stay in shape for her 21st Bike MS in October!  Our Above and Beyond winner, raised over $34,000 last year for her ride from over 200 donors, bringing her overall fundraising total to $236,340.28.  She has also served on the Bike MS fundraising committee for the past several years.


Thank you for your generous support. We are excited to celebrate with you safely at the 2021 New Orleans On the Move event at the Elms Mansion on September 30, 2021. We've planned every detail of this event with the health and safety of our attendees, volunteers, and staff as our highest priority. Safety protocols are in place that follow current guidance from the CDC, as well as state, city and other local agencies. This includes mandatory face coverings, regardless of vaccination status, reduced touchpoints to minimize physical interactions, and adhering to capacity limits of the venue. Please note that plans may be altered as the event day approaches to ensure your safety. We will provide additional information as it becomes available. Please click here for more of what to expect at the event.


The National Multiple Sclerosis Society exists because there are people with MS. Our vision is a world free of MS. Everything we do is focused so that people affected by MS can live their best lives as we stop MS in its tracks, restore what has been lost and end MS forever.


We are more than an organization. We are a movement. United in our collective power to do something about MS now and end this disease forever. The gathering place for people with MS, their family and loved ones, healthcare providers, volunteers, donors, fundraisers, advocates, community leaders and all those that seek a world free of MS. A place to connect and take action. In order to change the world, we mobilize all possible human and financial resources to achieve results.


Hosted By

National Multiple Sclerosis Society - New Orleans
For more information please contact: Kate Schroeder


Elms Mansion, 3029 St Charles Ave, New Orleans, LA 70115, USA

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