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Science

Trees for me, we and thee: What's behind the growing push for 'tree equity'

Most of us don't think of trees as a measure of social justice, but it's a real thing.

tree equity, environmental justice

Wealthy areas have up to 65% more tree cover than lower-income communities.

When we talk about environmental justice, we usually talk about how vulnerable communities are disproportionately impacted by things like contaminated water, air pollution, toxic living conditions and lack of access to healthy food. We aren't usually referring to about how many trees someone has around them on a regular basis, but a push for "tree equity" indicates that maybe we should.

That's right, tree equity. It's a real thing.

The impact that trees have on our daily lives is significant. Not only do trees provide natural beauty that brings us joy and comfort, but they absorb carbon dioxide and other air pollutants, release oxygen, provide cooling shade, filter drinking water and support wildlife. Being near trees helps us live healthier lives in various ways, but some people see more of these benefits than others.

In fact, according to the non-profit group American Forests, wealthy areas have 65% more tree cover than lower-income areas nationwide in the U.S., and it's especially an issue in our cities.


"The inequitable distribution of trees exacerbates social inequities," American Forests shares on its website. "A map of tree cover is too often a map of income and race—especially in cities. That’s because trees often are sparse in low-income neighborhoods and some neighborhoods of color. In fact, policies from the early 1900s are still shaping the way redlining contributes to periods of disinvestment, exacerbating tree inequity in these neighborhoods."

The "tree equity" project aims to minimize these disparities so that everyone can reap the health, economic and other benefits trees provide. Through calculating a "tree equity score" derived from tree canopy cover, climate, demographic and socioeconomic data in 486 Census-defined Urbanized Areas, the project aims to prioritize planting trees in neighborhoods that need them the most.

And cities are stepping up to the plate. Washington, D.C., now boasts an overall tree equity score of 91 out of 100—one of the best in the nation—but it took concerted, sustained effort to get there. Decades of disinvestment in the 70s and 80s led to a profound reduction in tree cover in the city, and by the late 1990s, the impact of that disinvestment was clear. In 1999, the Washington Post’s Metro section shared two aerial photos of the city, one from 1973 and one from 1997, showing how the landscape had changed over that time and people were shocked.

"The story needed no words," shares American Forests. "From the perspective of the 30-meter resolution available at the time, one image was predominantly green, the other looked like a tornado had ripped through a majority of the nation’s capital."

The stark difference between those images sparked a citywide conversation about priorities, and a push for more vegetation ensued. The city created an Urban Forestry Administration with a robust budget for getting the city's tree canopy thriving. And according to D.C.'s current tree equity score, it has worked.

On the other side of the country, the other Washington is also investing in trees, which may seem ironic considering its nickname as The Evergreen State and Seattle's "Emerald City" moniker. Trees have always been a big part of Washington's identity, but that doesn't mean its overall tree equity score is good. The interactive tree equity score map shows neighborhoods around Seattle ranging from a perfect score—100 out of 100—all the way down to 16 out of 100.

According to Grist, Washington has initiated the nation's first statewide tree equity project, the Washington Tree Equity Collaborative, bringing together city governments, Native tribes, community groups, businesses and researchers to expand the tree canopy in Washington’s urban areas with a focus on underserved populations.

Washington’s commissioner of public lands Hillary Franz said in a statement, “We must invest like never before, in order to ensure our most vulnerable communities have cleaner air and are better protected from extreme heat."

Grist offers a specific example of tree inequity in Seattle: Wealthy neighborhoods along Puget Sound and Lake Washington tend to have a lot of trees, while lower-income areas of south Seattle do not. Some communities will naturally have more trees due to proximity to water or natural topography, of course, but an analysis from Seattle’s Office of Planning and Community Development found that the most disadvantaged communities have been losing tree coverage 11 times faster than the least disadvantaged. That's an equity issue.

With climate change leading to more deadly heat waves in the American West, trees have become even more vital. The shade provided by trees can lower surface temperatures by double digits, and the evaporative properties of tree leaves can lower overall temperatures by as much as 9 degrees Fahrenheit. Lowering temperatures reduces energy use, which in turn helps lower pollution and increase air quality and even helps reduce the costs of street pavement maintenance since excessive heat makes pavement break down more quickly.

Of coure, the flip side of thee relationship between climate change and trees is that extreme weather events put a lot of stress on trees. Heat waves, droughts, strong storms, fires—not exactly ideal conditions for trees to thrive in overall. Even in areas where climate change may appear to be having a positivite impact on tree growth, researchers have found that pollution and higher temperatures are making trees larger, but weaker.

There's no question, however, that planting more trees is a good thing. Seattle's current plan will see three new trees planted for every healthy, site-appropriate tree removed from city property and two trees planted for every tree that dies or is deemed hazardous or invasive. And over the next five years, the city plans to plant 8,000 trees on public and private properties and 40,000 trees in parks and natural areas, with underserved communities being prioritized.

We all deserve the benefits trees have to offer. To learn more about tree equity and projects to build more tree cover and find out how you can help, visit the American Forests website.

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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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Sorry, Labradors. After 31 years, America has a new favorite dog.

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via Pixabay

A sad-looking Labrador Retriever

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America's Got Talent/Youtube

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