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.


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Hope is still here. It shows up in the research, in the resilience of those living with MS, and in the people who refuse...
04/10/2026

Hope is still here. It shows up in the research, in the resilience of those living with MS, and in the people who refuse to stop fighting for a better future.

Every step forward matters. Every breakthrough matters. Every voice matters.

Together, we keep pushing toward a world without MS. 💙

04/09/2026

When Siedah Garrett first heard Nancy Davis mention MS at a dinner party, it stopped her in her tracks, because she had been quietly carrying that same diagnosis for years.

She hadn’t told anyone. She didn’t want to be treated differently.

But that moment opened the door to something bigger.

Since then, Siedah Garrett has used her voice, her talent, and her time to support Race to Erase MS, helping bring awareness to the reality that a person can live with MS and still be fully functional, still create, still serve, and still live a powerful, meaningful life.

That is why her story matters. That is why this fight matters. 💙

Hope is not standing still and neither is MS research. Every new discovery brings us closer to better treatments, more p...
04/08/2026

Hope is not standing still and neither is MS research. Every new discovery brings us closer to better treatments, more personalized care, and a future we can all fight for. Progress matters. Research matters. And so does every person impacted by MS. 💙

Share this to remind someone that hope is still rising.

Closer than ever to a cure 💙Join leading doctors as they share the latest breakthroughs in MS research and care.Free + o...
04/07/2026

Closer than ever to a cure 💙

Join leading doctors as they share the latest breakthroughs in MS research and care.

Free + open to the public
Attend in person or virtually
Register: link in bio

04/06/2026

Research is moving, and the future of MS care is getting more personal.

From studying what individual cells in the brain are doing, to learning more about astrocytes and how they change, to understanding why MS can affect different populations in different ways, one thing is clear: we are stepping into a new era of possibility.

This matters because MS is not one-size-fits-all. The more we understand the genetics, biology, and lived experience behind how this disease shows up, the closer we get to more personalized care, better outcomes, and real hope for the future.

These are exciting times in MS research, and every breakthrough brings us one step closer.

What gives you the most hope when you hear about advances like this? Drop it in the comments and share this with someone who needs to hear that progress is happening. 💙

2.9 million people worldwide are living with multiple sclerosis. that number is not just a statistic, it represents moth...
04/03/2026

2.9 million people worldwide are living with multiple sclerosis. that number is not just a statistic, it represents mothers, fathers, children, friends, and neighbors fighting a battle most people cannot see.

Multiple sclerosis does not discriminate. It strikes without warning, and it affects every aspect of a person's life. But here is what gives us hope: research is changing the game.

Race to Erase MS has been on the front lines for over 30 years, funding groundbreaking research through our Center Without Walls program that connects the world's top MS research institutions.

Every dollar raised goes directly toward finding better treatments and ultimately, a cure.

2.9 million reasons to keep fighting. Zero reasons to stop.

Learn more and support the mission at RaceToEraseMS.org (link in bio)

Hope is built together 💙Join our inspiring panel of doctors as they share the latest advances in MS research and patient...
04/01/2026

Hope is built together 💙

Join our inspiring panel of doctors as they share the latest advances in MS research and patient care—and how we’re getting closer to a cure.

This is your chance to learn, connect, and be part of the progress.

Free & open to all
Join us in person or virtually
Register: link in bio

03/31/2026

What if the biggest breakthrough in MS treatment… isn’t a drug… it’s intelligence?

Not human. Artificial.

Dr. Peter Calabresi is talking about it… and this isn’t future talk. This is happening RIGHT NOW.

AI is already changing what it looks like to sit in a doctor’s office.
No more doctors buried in a screen while you’re trying to explain what’s going on.
Visits can now be recorded, summarized, and turned into accurate notes in real time… so your doctor can actually focus on YOU.

But that’s just the front end.

Behind the scenes, AI is doing something even bigger…

Instead of researching one question at a time over years,
we can now analyze massive datasets—DNA, RNA, proteins—all at once.

We’re not asking one question anymore…

We’re asking 10,000 at a time.

And in that chaos of data… patterns are emerging that humans alone would never catch.

That’s where real breakthroughs in MS research and treatment are starting to happen.

This isn’t hype.
This is acceleration.

The kind that compresses years into moments…
and gives people fighting MS something real: momentum.

If this hits home for you or someone you love… this matters.

Drop a 💙 if this gives you hope
or share this with someone who needs to see where things are headed 👇

Closer than ever to a cure 💙Join leading doctors as they share the latest breakthroughs in MS research and care.Free + o...
03/30/2026

Closer than ever to a cure 💙

Join leading doctors as they share the latest breakthroughs in MS research and care.

Free + open to the public
Attend in person or virtually
Register: link in bio

03/30/2026

What if we could stop MS before it ever starts?

Imagine identifying who is susceptible to multiple sclerosis and getting them on treatment before their very first attack before the damage is done. Because sometimes, that first attack can be devastating, and full mobility may never return.

That is the future Race to Erase MS is fighting for.
Not just better treatments but prevention.
Isolating those at risk and intervening before MS ever takes hold.

This is why research matters. This is why your support matters.
This would be amazing and it is possible.

Learn more at RaceToEraseMS.org (link in bio)

Every step is a victory when you are fighting MS.Walking to the mailbox. Making dinner. Playing with your kids. For some...
03/27/2026

Every step is a victory when you are fighting MS.

Walking to the mailbox. Making dinner. Playing with your kids. For someone living with Multiple Sclerosis, these are not small things. They are everything. And every single day you choose to keep going, you are winning.

MS does not just affect movement. It affects energy, vision, memory, and the ability to do the things most people take for granted. But the strength of the MS community is extraordinary. Every day, warriors wake up and fight battles that no one else can see.

This Friday, we want to celebrate every victory, no matter how small it may seem to the outside world. Because there is no such thing as a small victory when you are living with MS.

Share this for every MS warrior who turned an ordinary day into an extraordinary victory. Tag someone who never gives up. Tag someone who inspires you to keep fighting.

At Race to Erase MS, we are committed to funding the research that will one day make these daily battles a thing of the past.

Join the race at erasems.org. Link in bio.
March is MS Awareness Month. Let us make every moment count.

Some days, just getting out of bed is the bravest thing you can do.Living with MS means some mornings your legs don't co...
03/26/2026

Some days, just getting out of bed is the bravest thing you can do.

Living with MS means some mornings your legs don't cooperate. Your body feels like it belongs to someone else. The fatigue is so heavy it feels like gravity doubled overnight.

But you get up anyway. You put your feet on the floor. You take that first step. Because you are stronger than MS will ever be.

At Race to Erase MS, we see that strength every single day. It's why we have spent over 30 years funding research through the Center Without Walls, connecting the nation's top MS researchers to develop treatments that give people their mornings back. From zero FDA-approved treatments to 25 and counting, your fight fuels our mission.

Tag someone living with MS who inspires you every single day. Let them know you see their strength, even on the days they can't.

Share this post. Start a conversation. Join the race at erasems.org (link in bio)

Address

1875 Century Park E, Ste 280
Los Angeles, CA
90067

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm
Saturday 9am - 5pm
Sunday 9am - 5pm

Telephone

+13104404842

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