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3 reasons more and more states are outlawing daily fantasy sports sites like FanDuel.

If you've watched an NFL game this year, chances are you've seen at least one ad for either DraftKings or FanDuel.

Probably, you've seen more like 17 hojillion. Photo by Scott Olson/Getty Images.


You probably know that they allow users to bet on fantasy sports — and maybe earn (or more likely, lose) a few bucks here and there. What you might not know is that these sites have come under increased legal scrutiny in the past few months.

Nevada banned the sites from operating in-state back in September. And just today, the attorney general of New York ordered both DraftKings and FanDuel to stop taking bets in that state while his office investigates the legality of each business.

What's the deal? Why is fantasy football — of all things — attracting the attention of the law? It basically boils down to three things.

1. An employee cheating scandal makes the whole thing look ... kinda shady.

Photo by Donald Miralle/Getty Images.

In theory, fantasy sports are a level playing field. You put in your money and choose your players and/or teams, and you're promised an equal shot at winning a monetary prize. It's a system that works ... as long as everyone has the same information.

Increasingly, that's looking like it might not be the case with DraftKings and FanDuel.

In September, an employee of DraftKings won $350,000 in a competition at competitor site FanDuel — the same week he accidentally released a bunch of insider data online — which made it seem like people who work for daily fantasy sports sites might be operating with more information than the average player. According to some reports, executives and employees of the two companies are some of the top bettors on their rivals' platforms.

Ultimately, the employee was cleared — internally — of wrongdoing. But it prompted the FBI to launch an investigation, which is ongoing.

2. Unlike most gambling, the daily fantasy sports industry is pretty much completely unregulated.

Photo by Scott Olson/Getty Images.

Gambling is a heavily supervised industry in most states and on the Internet. A 2006 law prohibits most forms of betting online. Online fantasy sports are exempt from the law, however, as "games of skill" are not technically considered gambling under the law.

Why is fantasy football a game of skill? It's ... not entirely clear. Evaluating player and team statistics — and making judgments based on that analysis — certainly requires specific knowledge. You could probably say the same for more traditional gambling platforms like horse racing and poker. But it doesn't really matter. Under the law, right now, it's considered one.

Without the same government oversight that comes with running a traditional casino or other gambling operation, daily fantasy sports could be vulnerable to hacking, cheating, insider betting, and other such bad behavior that potentially makes the contests lopsided, unfair, and not-as-advertised.

Conventional gambling outfits certainly aren't always beacons of honesty and fairness even with oversight, but right now, daily fantasy sports are subject to none. And that's a problem.

3. Gambling is a big public health issue, which is rarely addressed.

Slot machines. Photo by Philippe Lopez/Getty Images.

To hear representatives from DraftKings and FanDuel tell it, daily fantasy sports are not gambling. Which — as today's New York Times report makes clear — is news to New York Attorney General Eric T. Schneiderman, who launched the most recent investigation of the sites:

"The attorney general's office said daily fantasy sports 'appears to be creating the same public health and economic problems associated with gambling.'"

More casinos are closer to more Americans than ever before. Studies estimate 1.1-1.9% of the population — between 3.5 and 6 million people — suffers from some form of gambling addiction. And low-income Americans are particularly vulnerable, as their losses can be far more catastrophic. Many experts believe that, as a potential source of addiction, fantasy sports are indistinguishable from other forms of gambling. Now that they're available at the click of a button, the barrier to entry is suddenly extremely low, and the potential to lose hundreds or thousands of dollars is high.

Fantasy sports can be fun and harmless — but more oversight is a good thing.

For those who play — and even place the odd bet here and there — fantasy sports can be a rewarding hobby. Gambling a little bit of money with your friends or even random strangers on the Internet is fun! But betting through an easily hackable, unregulated system where employees might have access to information that you don't? Not to mention one that can be an emotionally and financially devastating if abused?

Seems like it might be a good idea to stay away until a few more rules are put in place.

Taking a look under the hood of the industry is long overdue. Hopefully, a thorough investigation can make the system fairer, more transparent, and, most importantly, work better for everyone.

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Three women, three MS journeys: How multiple sclerosis looks different for everyone

Gina, Nathalie and Helga share their reactions to being diagnosed with MS and how they stay informed and positive in the face of ever-changing symptoms.

Courtesy of Sanofi

Helga, Nathalie and Gina all have MS, and their experiences show how differently the disease can manifest.

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It’s been 155 years since neurologist Jean-Martin Charcot gave the first lecture on a mysterious progressive illness he called “multiple sclerosis.” Since then, we’ve learned a lot. We know MS causes the immune system to attack healthy tissue, including damaging the brain and spinal cord. Resulting symptoms can be debilitating and include fatigue, blurred vision, memory problems and weakness. Huge advancements in our understanding of MS and its underlying causes, as well as treatment advances, have been made in the past few decades, but MS remains a complex and unpredictable reality for the 2.8 million+ people diagnosed around the world.

Ironically, the only real constant for people living with MS is change. There’s no set pattern or standard progression of the disease, so each person’s experience is unique. Some people with MS have mild symptoms that worsen slowly but sometimes improve, while others can have severe symptoms that drastically alter their daily lives.

All people with MS share some things in common, however, such as the need to stay informed on the ever-evolving research, find various lines of support and try to remain hopeful as they continue living with the disease.

To better understand what navigating life with MS really looks like, three women shared their MS stories with us. Their journeys demonstrate how MS can look different for different people and interestingly, how the language used to talk about the disease can greatly impact how people understand their realities.

woman with horse, woman riding horseGina loves riding her horse, Benita.Courtesy of Sanofi

Gina—Hamburg, Germany (diagnosed with relapsing multiple sclerosis in 2017)

When her youngest son was 4 months old, Gina started having problems with her eye. She’d soon learn she was experiencing optic neuritis—her first symptom of MS.

“Immediately after the diagnosis, I looked up facts on MS because I didn’t know anything about it,” Gina says. “And as soon as I knew what could really happen with this disease, I actually got scared.”

As her family’s primary income provider, she worried about how MS would impact her ability to work as a writer and editor. Her family was afraid she was going to end up in a wheelchair. However, for now, Gina’s MS is managed well enough that she still works full-time and is able to be active.

“When I tell somebody that I have MS, they often don't believe me the first time because I don't fulfill any stereotypes,” she says.

Overwhelmed by negative perspectives on living with MS, Gina sought support in the online MS community, which she found to be much more positive.

“I think it’s important to use as many positive words as you can when talking about MS.” It’s important to be realistic while also conveying hope, she says. “MS is an insidious disease that can cause many bad symptoms…that can be frightening, and you can't gloss over it, either.”

To give back to the online community that helped her so much, Gina started a blog to share her story and help others trying to learn about their diagnosis.

Though she deals with fatigue and cognitive dysfunction sometimes, Gina stays active swimming, biking, riding horses and playing with her sons, who are now 11 and 6.

Cognitive dysfunction is common in MS, with over half of people affected. It can impact memory, attention, planning, and word-finding. As with many aspects of MS, some people experience mild changes, while others face more challenges.

Gina says that while there’s still a lot of education about MS needed, she feels positive about the future of MS because there’s so much research being done.

woman in wheelchair holding medal, woman rowingNathalie is an award-winning rower with multiple international titles.Courtesy of Sanofi

Nathalie — Pennes Mirabeau, France (diagnosed with relapsing-remitting multiple sclerosis in 2002)

Nathalie was a teenager and a competitive athlete when she noticed her first symptoms of MS, but it would take four years of “limbo” before she was diagnosed.

“Ultimately, the diagnosis was more of a relief, than a shock,” she says. “Because when you have signs and you don’t know why, it’s worse than knowing, in the end, what you have.”

However, learning more about the disease—and the realities of disease progression—scared her.

“That glimpse of the future was direct and traumatic,” she says. Her neurologist explained that the disease evolves differently for everyone, and her situation might end up being serious or very mild. So, she decided to stop comparing herself to others with MS.

She said to herself, “We’ll see what happens, and you’ll manage it bit by bit.”

By 2005, Nathalie’s MS had progressed to the point of needing a wheelchair. However, that has not dampened her competitive spirit.

Nathalie began her international rowing career in 2009 and has won multiple world titles, including two Paralympic medals—silver in London and bronze in Tokyo. Now, at 42, she still trains 11 times a week. Fatigue can be a problem, and sometimes hard workouts leave her with muscle stiffness and shaking, but she credits her ongoing sports career for helping her feel in tune with her body’s signals.

“Over the years, I’ve learned to listen to my body, letting my body guide when I need to stop and take breaks,” she says.

Nathalie explains that she used to only look backwards because of the initial shock of her diagnosis. In time, she stopped thinking about what she couldn’t do anymore and focused on her future. She now lives in the following mindset: “Even when doors close, don’t miss out on those that open.” Instead of focusing on what she can’t do, she focuses on the opportunities she still has. Right now, this includes her training for the 2024 Paralympic Games in Paris, where she will compete for another rowing medal.

“I only go forward,” she says. “Well, I try, anyway…It’s easy to say, it’s not always easy to do. But that’s what I try to do.”

woman exiting water after swimming, woman with great daneHelga's Great Dane has become a helpful and beloved companion.Courtesy of Sanofi

Helga—Johannesburg, South Africa (diagnosed with relapsing multiple sclerosis in 2010)

When Helga first started having balance issues and numbness in her feet, she chalked it up to her training as a runner. But when the numbness moved to her face, she knew something was wrong. She never guessed it was MS.

“When I was diagnosed, I felt completely overwhelmed and clueless,” Helga says. “I felt that I had nowhere near enough information. I did not know anything about the disease…I had no idea that it was going to be a process of continually monitoring and adjusting your lifestyle.”

In the beginning, Helga’s symptoms developed slowly, and she didn’t appear ill to others. She was even able to run for a few years after her diagnosis, but she couldn’t do marathons anymore, and she began to fall frequently due to balance issues and right-foot dragging. Then her cognition issues became more problematic, especially in her job as a trainer in a printing company.

“My executive function, decision-making and short-term memory were affected to the point that I was eventually medically unfit for work,” she says. She stopped working in 2017.

However, she didn’t stop living life. Even though she could no longer run, she continued to swim competitively. She got a Great Dane puppy and trained him as a service dog to help her walk. She also serves as vice chair of the patient support organization Multiple Sclerosis South Africa, and she advises others who have been diagnosed to join a patient advocacy group as soon as possible to get reliable information and meet others with MS.

Helga says she is “hopeful” about the future of MS. “I must say that I am so grateful that we have all the new medications available, because my life would not be the same if it wasn't for that,” she adds.

Part of how she manages her MS is by looking at the positives.

“If I could tell the world one thing about MS, it would be that MS is an incurable disease of the nervous system, but it's also the greatest teacher of valuing your health, family, friends, and managing change in your life,” she says. “My life is diversified in a way that I never, ever thought it would, and MS has been honestly the greatest teacher.”

Each MS journey is unique – with each person impacted experiencing different struggles, successes, and feelings as they manage this unpredictable disease. But the common thread is clear – there is a critical need for information, support, and hope. We are proud to participate in World MS Day and share these incredible stories of living life while living with MS. To learn more about MS, go to https://www.sanofi.com/why-words-really-matter-when-it-comes-to-multiple-sclerosis.

MAT-GLB-2301642-v1.0-05/2023

This article was sponsored by Sanofi. Participants were compensated when applicable.

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