Race to Erase MS

Race to Erase MS Dedicated to the treatment and ultimate cure of Multiple Sclerosis. Research is our core focus. We are now so much closer to finding a cure.
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The Nancy Davis Foundation for Multiple Sclerosis was founded by Nancy Davis in 1993 after being diagnosed with multiple sclerosis. After her diagnosis, she was determined to devote her time and resources to finding a cure. Nancy’s hope, courage and strength continue to inspire her to maintain a vibrant quality of life despite this chronic disease, but most of all, she remains positive, continues to live her life to the fullest and is tireless in her efforts to finding the cure for MS. In the process of learning all she could about multiple sclerosis, she discovered that MS affects close to two million Americans primarily between the ages of 20 and 40, and three times as many women as men, Nancy Davis made it her deep personal commitment to help find the cause and ultimately the cure of this disease. In 1993 she founded The Nancy Davis Foundation for Multiple Sclerosis and held the first Race to Erase MS event – an intimate ski getaway weekend in Aspen, Colorado – that pulled in over $1.3 million for the Foundation. Since its inception, the Race to Erase MS has become an exciting star-studded gala. The foundation has gained the support of many key individuals in the fashion and entertainment worlds, including Tommy Hilfiger who has been a major sponsor since 1997 and who has a sister living with MS. The annual Race to Erase MS event has raised over $30 million for multiple sclerosis research to date. All proceeds directly fund the foundation’s Center Without Walls program, a selected network of the nation’s top seven MS research centers. This nationwide collaboration of physicians, scientists and clinicians are on the cutting-edge of innovative research programs and therapeutic approaches to eradicate MS. The Centers work as a team constantly communicating, never duplicating. It was the goal of Nancy Davis to build a winning team and the Foundation sought out the best and the brightest MS research facilities throughout the world. It is the hope of her Foundation that in addition to combating MS through research in a clinical environment, that an increased awareness will be created by educating the public about this devastating disease.

“While there’s no cure for MS yet, we have broken so much new ground in a very short time and we will not stop until we cross the finish line and find a cure for MS,” Nancy explains. It’s amazing how the landscape has significantly changed over the years. At the time Nancy was diagnosed is 1993, there were no drugs on the market to help stop the progression of this disease. Miraculously, there are now six with FDA approval with a seventh very near approval and others to be approved in the very near future. This expansion of minds working towards a cure gives individuals the confidence that MS may in fact be erased in the next decade with the diligent work of the Center Without Walls physicians and the continued support of the many generous and caring contributors to this cause.


**DISCLAIMER**
The contents of the Nancy Davis Foundation Facebook Fan Page, such as text, graphics, images, and other material contained on the Site ("Content") are for informational purposes only. The Content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on the eMedicineHealth Site! If you think you may have a medical emergency, call your doctor or 911 immediately. The Nancy Davis Foundation does not recommend or endorse any specific tests, physicians, products, procedures, opinions, or other information that may be mentioned on the Site. Reliance on any information provided by the Nancy Davis Foundation, Nancy Davis Foundation employees, others appearing on the Site at the invitation of the Foundation, or other visitors to the Site is solely at your own risk.

12/29/2025

Dr. Christopher Orlando has been part of our Center Without Walls team since his fellowship at USC. Now a new USC faculty member and a Race to Erase MS Young Investigator awardee, he shares how vital our community’s support is in accelerating MS research.

Less than 72 hours left to make a tax-deductible gift for 2025. Contribute today: https://shop.erasems.org/products/race-to-erase-ms-donation-1

12/06/2025

12/05/2025

Center Without Walls Symposium

Giving Tuesday is here! Every dollar fuels MS research, empowers breakthroughs, and brings us closer to a cure. Join us ...
12/02/2025

Giving Tuesday is here! Every dollar fuels MS research, empowers breakthroughs, and brings us closer to a cure. Join us in funding the science and making a difference today. Visit the links in our bio and story to learn more about the ways to contribute today!

We’re proud to recognize Joseph Sabatino, MD, PhD as a recipient of our Race to Erase MS Innovation Award. For decades, ...
12/01/2025

We’re proud to recognize Joseph Sabatino, MD, PhD as a recipient of our Race to Erase MS Innovation Award.

For decades, scientists have known that infection with the Epstein–Barr virus (EBV) is strongly associated with the development of multiple sclerosis. EBV is incredibly common and usually remains dormant, but it can periodically reactivate. While EBV is now understood to be a key risk factor for developing MS, its role after the disease begins remains a major unanswered question.

Dr. Sabatino’s research seeks to understand whether EBV reactivation may be linked to worsened long-term MS outcomes. His study will examine EBV activity, along with antibody and T-cell responses in the blood of patients with stable MS compared to those whose disease has progressed.

This work will help determine whether EBV reactivation contributes to inflammation in MS or perhaps even triggers disease worsening.

This is the kind of critical, future-shaping research your support makes possible. Make an early donation in honor of Giving Tuesday at: erasems.org or the link in our bio!

We’re proud to recognize Christopher Orlando, MD, as a recipient of our Race to Erase MS Innovation Award. A timely diag...
11/30/2025

We’re proud to recognize Christopher Orlando, MD, as a recipient of our Race to Erase MS Innovation Award.

A timely diagnosis is critical for people living with multiple sclerosis. When MS goes unrecognized or untreated, symptoms can worsen, leading to greater long-term disability. Dr. Orlando’s important research focuses on understanding why some individuals experience significant delays before receiving a diagnosis and starting treatment.

His study examines the full landscape of potential barriers:
- Patient-based factors: insurance coverage, travel distance to care, and other access-related challenges.
- Healthcare system factors: such as whether a person can see a neurologist early in the process.
- Physician-based factors: including the MS knowledge of the first doctor a patient sees whether a neurologist or an emergency department provider.

The research will also explore whether pre-existing conditions like high blood pressure and cardiovascular disease contribute to diagnostic delays across different healthcare systems. The goal is to identify at-risk groups and create real, workable interventions to ensure everyone with MS receives timely, equitable care.

Thanks to our supporters, Race to Erase MS can fund critical research like this, helping more people get the early diagnosis and treatment they need. Make an early donation in honor of Giving Tuesday at: erasems.org or the link in our bio!

Join us for a day of hope, breakthroughs, and connection. The MS Forum & Expo brings together top researchers, medical e...
11/26/2025

Join us for a day of hope, breakthroughs, and connection. The MS Forum & Expo brings together top researchers, medical experts, and the MS community to share the latest advances in research and support. This event is free and open to the public, register at erasems.org or at the link in our bio!

The countdown to Giving Tuesday is on! ⏰ Your early gift ensures their vital work continues donate at erasems.org or at the link in our bio.

Join us for the MS Forum and Expo, a day of hope, breakthroughs, and connection as we explore the latest in MS research ...
11/19/2025

Join us for the MS Forum and Expo, a day of hope, breakthroughs, and connection as we explore the latest in MS research and patient innovation.

In-person and virtual registration available at: erasems.org/ms-forum-expo/
If you’re attending in person, here’s a special treat: the first 30 people to register for in-person attendance will receive a gift at the event.

We’re heartbroken to learn of the passing of Loni Anderson, a true icon and cherished friend of Race to Erase MS. Her ge...
08/04/2025

We’re heartbroken to learn of the passing of Loni Anderson, a true icon and cherished friend of Race to Erase MS. Her generous spirit and unwavering support of our mission to find a cure for MS touched so many lives. We are forever grateful for her kindness, compassion, and commitment. She will be deeply missed. 💙🧡

06/22/2025

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1875 Century Park E, Ste 280
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90067

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