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There's an unexpected downfall to banning plastic straws. Here's what to consider.

Cities are starting to ban plastic straws in an effort to minimize waste. Great news, right?

Well, that depends.

Nobody likes waste, but sometimes in our rush to eliminate it, we don't think through the consequences of our actions. Take, for example, the push to ban plastic straws.


As of July 1, restaurants in Seattle are banned from giving customers non-recyclable plastic utensils or straws. Restaurants can still provide customers with a number of durable or compostable utensils or straws upon request.

Other cities that have banned or restricted the use of straws include Edmonds, Washington; Miami Beach and Fort Myers Beach, Florida; Monmouth Beach, New Jersey; and a slew of California towns including Alameda, Berkeley, Carmel, Davis, Malibu, Manhattan Beach, Oakland, Richmond, and San Luis Obispo.

[rebelmouse-image 19346017 dam="1" original_size="750x436" caption="Photo by Ayotunde Oguntoyinbo/Unsplash." expand=1]Photo by Ayotunde Oguntoyinbo/Unsplash.

But for some people, the disappearance of plastic straws is really bad news.

Flexible, single-use plastic straws are what make it possible for many disabled people to drink beverages. Eliminating them means requiring people to drink directly from the lip of their cup — a function that many disabled people simply aren't able to perform.

Many have suggested commonsense alternatives to plastic straws, like paper or metal ones. But in an interview with iNews, Scottish disability rights activist Jamie Szymkowiak explained exactly why popular alternatives don't meet the needs of some disabled individuals.

Permanent straw options, like metal or bamboo, are too hard for some people who rely on the flexibility of a plastic straw. (Injury is also a risk.) Biodegradable paper straws have a tendency to disintegrate when placed into heated drinks — which can pose a hazard of its own — and porous silicone straws require cleaning immediately after use.

Some might ask why people who need access to old-school plastic straws don't just purchase and bring their own wherever they go.

And sure, that is technically a solution. But making disabled people pay for something that's available to everyone else for free is a type of tax. While it's not necessarily an expensive tax, these types of things add up, and implementing a policy that makes the simple act of drinking prohibitive to certain groups sets a bad precedent.

[rebelmouse-image 19346018 dam="1" original_size="750x437" caption="Photo by Horia Varlan/Wikimedia Commons." expand=1]Photo by Horia Varlan/Wikimedia Commons.

The real problem is that cities considering restrictions simply aren't taking disabled voices into account.

Gabrielle Peters, a disabled writer living in Vancouver, has been keeping tabs on her city's plans to ban straws. What's concerning to her is that even after disability advocates presented information to elected officials, she felt their concerns were largely ignored.

Also troubling to Peters is the fact that the specific push to ban straws appears to be driven by a viral video about a turtle with a straw stuck in its nostril rather than on researched facts and statistics.

"We should feel compelled to act," she says. "But it is essential we temper our emotional response with considered thought so we don't respond in a way that ends up doing something that causes additional, different, and potentially more widespread suffering."

Peters' solution is simple: "People who don’t need straws should not use them. People who do should."

"We need to make straws accessible to those who need them," she says. "Don't turn them into a medical item, which will negatively affect availability and lead to increased expense and stigma."

As someone with dysphagia, a condition marked by a difficulty swallowing, Peters has at points relied on straws to avoid burns, broken glasses, and spilled drinks. (She's careful to note, though, that straws won't necessarily help all people with dysphagia.)

"Our solutions and adaptations are not something you can neatly chart. We figure out what works for our bodies AND our lives," she says.

In this case, that might mean people who don't need straws voluntarily choosing not to use them while also letting them remain available for those who do.

This photo shows an injured Marine, but it's important to remember that disability takes many forms and isn't necessarily something the average observer can see in someone else. Photo by Alex Wong/Getty Images.

It's important to look clearly at a problem before jumping to a  "solution" that doesn't actually make sense.

Maybe a plastic straw ban wouldn't personally affect you; maybe it seems like a small price to pay if it has a big impact on improving the health of the world's oceans. But here's the thing: It doesn't!

What makes the entire debate over straws that much more confusing is the fact that disposable straws don't actually contribute much to the abundance of plastic waste relative to other items in the ocean. So by proposing a ban on them, we're asking disabled people to sacrifice a lot in order to gain just a little in the fight for environmental health. And by doing that, we're demonstrating a frightening lack of empathy.

As a society, we are far too quick to write off the concerns of marginalized groups as insignificant or inconvenient.

The next time someone comes to you with a concern, especially if it relates to inclusion or accessibility, try to make a real effort to actually hear what they have to say, and then maybe ask yourself why something like banning a plastic straw is so important to you, anyway.

If we can't take care of each other, we can't take care of the earth. So let's start there.

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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.

True

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.

@thehalfdeaddad/TikTok

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Single dadPatrick Forseth recently shared how he made a truly teachable moment out of his son, Lincoln, getting into trouble for bullying. Rather than forcing an apology, Forseth made sure his son was actively part of a solution.


The thought process behind his decision, which he explained in a now-viral TikTok video, is both simple and somewhat racial compared to how many parents have been encouraged to handle similar situations.
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Guy with 90s-style radio show on TikTok is actually changing lives for aspiring musicians

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This guy rocks.

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As is the way with many TikTok sensations, faux radio show “The Bun 91.3” started off as a fun hobby. The DJ, known only to listeners as “The Bun,” highlights songs by up-and-coming artists all while sporting aviator sunglasses and mastering that cheesy, old-school radio voice.

Much to his surprise, The Bun’s passion project has actually been bringing major attention to aspiring musicians who might otherwise go unnoticed, just like real radio shows did back in the day.

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Typically, whoever babysits for you is solely there to focus on the well-being of your children. They feed them snacks, play games with them, and follow their bedtime routine to the letter. Then they hang out on your couch reminding Netflix that they're still watching and wait for you to return. Sure, they clean up dishes from dinner and whatever toys were pulled out during their time with your kids, but they don't typically clean your house.

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Barack Obama speaking at the World Travel & Tourism Council, 2019

If you’re looking for career advice, there are few better people to ask than former President Barack Obama. After all, he got the most prestigious job in the world after only spending four years in the U.S. Senate and seven in the Illinois State Senate.

Obama clearly knows how to work his way up in the world.

Now, he’s investigating what it means to have “good” work in his new Netflix show, “Working: What We Do All Day.” According to Netflix, the show explores compelling ideas and issues about labor and work, while focusing on the lives of individuals in various professions.

Obama sat down with LinkedIn Editor-in-Chief Daniel Roth to talk about employment-related topics, including the role of work in our lives, disruptions in the workplace in the new Millenium, and the coming AI revolution. During the 15-minute conversation, Obama shared his most important career advice for young people, and it was simple, especially for such a thoughtful, well-spoken man. The former president said, “Get stuff done. Just learn how to get stuff done.”

He then unpacked what he meant by his simple motto.

“I've seen at every level people who are very good at describing problems, people who are very sophisticated in explaining why something went wrong or why something can't get fixed, but what I'm always looking for is, no matter how small the problem or how big it is, somebody who says, 'Let me take care of that,'” Obama said. “If you project an attitude of, whatever it is that's needed, I can handle it and I can do it, then whoever is running that organization will notice. I promise.”

Obama is spot-on with his analysis. You can talk about things all day, but what really matters is taking action and making things happen. Maybe that’s why his campaign slogan in 2008 was a simple three-word phrase about taking care of business, “Yes, we can.”

"The best way to get attention is, whatever is assigned to you, you are just nailing. You're killing it. Because people will notice, that's someone who can get something done," Obama continued.

As someone who has managed people at the top levels of government, Obama has a rare understanding of the importance of relying on people to carry out essential orders and knowing who to trust to get it done efficiently and correctly. When you’re president of the United States, you must have complete trust in the people you delegate work to because thousands or even millions of lives could be at risk.

Obama also added that young people shouldn’t focus on a specific job title but on things that interest them. "The people that I find are the most successful are the people who say, 'I'm really interested in computers and figuring this stuff out,' and they end up being a Bill Gates," he said.

People will be happier with careers that are rooted in their interests because they’re doing what they love. We only get 24 hours in a day. Most people sleep eight, work eight and enjoy eight for themselves. Everyone loves sleeping and time off, but you can be happy 24 hours a day when you love your job.

Photo by Andrew Gaines on Unsplash

Firefighter Jeff Ohs resuscitated Xavier Dimples as a toddler.

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