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There's been a quiet protest happening in the trees of Appalachia. Now, it's catching on.

When Abigail peeks out from her perch — a wooden platform dangling high in a tree on a mountain ridge in West Virginia — she sees a nearly picture-perfect landscape.

She points out roaming farm animals and watches cars drive the few country roads that border the Jefferson National Forest. "The sunsets are incredible," Abigail describes. "And it’s pretty peaceful when the winds aren’t too strong."

[rebelmouse-image 19532530 dam="1" original_size="800x600" caption="The view from Abigail's tree platform. Photo courtesy of Appalachians Against Pipelines." expand=1]The view from Abigail's tree platform. Photo courtesy of Appalachians Against Pipelines.


‌The 22-year-old Virginian (who asked us not to disclose her last name because of the risk involved in her protest) has called this sweeping landscape around Peters Mountain — and this one tree — home since she and others climbed up its branches on a mission on Feb. 26, 2018.

She chose the tree she’s in for a reason: It sits right where the Mountain Valley Pipeline is slated to carry natural gas through the fragile limestone terrain beneath its roots.

The construction of this pipeline would mean the destruction of this landscape, and Abigail is determined to stall that as long as possible.

The Mountain Valley Pipeline was first proposed in 2014 and has been met with community resistance every step of the way.

The route moves from north of Clarksburg, West Virginia, down to just southeast of Roanoke, Virginia — where it's been proposed it will continue another 70 miles south into North Carolina. The 42-inch-diameter pipeline will carry fracked natural gas, and residents like Becky Crabtree — who lives along the route and whose sheep Abigail can see from her tree — fear for their health, communities, and land.

Pipeline route map created by Upworthy.

"We can’t find record of a pipeline of this size ever being built on such a steep grade," Crabtree says. "There are so many questions we have, and no one is answering any of them for us."

Crabtree's property at the base of Peters Mountain is intersected by the pipeline, and her concerns about it are endless. She worries about sinkholes, about the quality of water reservoirs in the area, and about the construction traffic planned on her little one-lane road. She worries about the fence around her sheep field that she’ll have to pay to rebuild once MVP widens that road for their use. She worries about the effect the pipeline will have on the Appalachian Trail, which it will cross under just a couple hundred feet from Abigail’s tree.

[rebelmouse-image 19532532 dam="1" original_size="800x450" caption="The ridge of Peters Mountain from above Abigail's tree. Photo courtesy of FightingFox Photography." expand=1]The ridge of Peters Mountain from above Abigail's tree. Photo courtesy of FightingFox Photography.

Armed with many of the same concerns as Crabtree, over 400 landowners along the pipeline’s route refused to grant MVP easements on their property. These landowners were sued by MVP in 2017 for access to the land; eventually, a federal court will grant the private company access by condemning each person’s land through eminent domain, claiming that the pipeline serves a public good.

Upworthy reached out to MVP for a comment, but has not heard back.

Just a few dozen miles from Abigail, a 60-year-old woman nicknamed "Red" has also taken to the trees to stop pipeline construction on her family’s Virginia land.

"When I saw the tree sits on Peters Mountain," Red Terry says, "I knew what we had to do." Her husband’s family has lived on the Roanoke County land for generations, preserving the streams, wetlands, and an historic orchard that the pipeline will run right through.

"Everyone wants MVP’s money," she quips. "But there are some things in life worth a hell of a lot more than money."

Red's tree-sit, like Abigail's, has been surrounded by tree-felling in recent weeks. But the presence of the tree-sitters — along with dozens of supporters on the ground — has prevented MVP from cutting many trees in the pipeline's path. Although the community supporting these protests is vast, the threat of legal consequences has kept many, like Abigail, from disclosing personal information.

[rebelmouse-image 19532533 dam="1" original_size="2581x1936" caption="A protester blocks a MVP access road in Virginia. Photo courtesy of FightingFox Photography." expand=1]A protester blocks a MVP access road in Virginia. Photo courtesy of FightingFox Photography.

As construction ramps up, Red and Abigail aren’t the only ones taking direct action.

In Giles County, Virginia, a blockade was erected by pipeline opponents on an MVP access road. A single protester has been perched atop a 50-foot log placed vertically in the road for three weeks and counting, effectively halting construction of both the access road and the pipeline. She has not come down once, despite the continued presence of law enforcement preventing supporters from replenishing her supply of food and water. The banner hanging with her aptly reads: "The fire is catching: No pipelines."

Back in West Virginia, Crabtree says she was "jumping up and down delighted" to learn about the folks who climbed into the trees on Peters Mountain.

"We hadn’t noticed them until we read about them," she says. "But the more people that learn about them, the more admiration there is in the community. The more sense there is that we support people that ‘lay it down’ for our environment. That takes courage and wherewithal. It takes some extra teeth."

[rebelmouse-image 19532534 dam="1" original_size="800x672" caption="Photo courtesy of Appalachians Against Pipelines." expand=1]Photo courtesy of Appalachians Against Pipelines.

Local supporters have been so grateful for the tree-sitters that just a couple weeks ago, they held a spaghetti dinner fundraiser in support.

That evening, dozens of folks gathered in a church basement to eat, talk with friends and neighbors, and contribute to the cause on Peters Mountain. Crabtree’s granddaughters ran a table complete with markers and construction paper where well-wishers could write thank-you notes to be delivered up the ridge.

Up in her oak tree, Abigail recounts tales of the past three years, which she has spent opposing this pipeline.

“It got to the point where we had tried all these options to fight this,” she reports. “We talked to our representatives. We tried running our own candidates. We wrote letters to the editor. We had people sign petitions. Didn’t work, didn’t work, didn’t work. This is the only thing I feel like I have left.”

Sun is out and our batteries are happy. Hope you all are getting some ☀ too!bit.ly/supportmvpresistance

Posted by Appalachians Against Pipelines on Sunday, March 18, 2018

This fight comes at a time of widespread and increasing resistance to pipelines and other destructive fossil fuel projects around the country and the world.

Just east of the MVP route, folks are fighting the Atlantic Coast Pipeline, a natural gas pipeline that — among a multitude of other issues — has a compressor station planned for Union Hill, Virginia, a community built by the descendants of freed slaves.

Down in Louisiana, the Bayou Bridge Pipeline is scheduled to cross 700 bodies of water, including a reservoir that supplies drinking water to the United Houma Nation and 300,000 Louisiana residents. This is the tail end of the Dakota Access Pipeline, which thousands protested last year at Standing Rock.

The list goes on: Mariner East 2, Rover, Line 3, Trans Mountain. But so do the stories of people rising up in the face of this ongoing destruction of land and communities.

"I don’t have a lot to lose being in this tree," Abigail shares, as she settles into her sleeping bag for another night on the mountain. "But as a young person and person from this region, I do have a lot to lose with this pipeline."

Peters Mountain treesit in path of Mountain Valley Pipeline - with drone footage

Check out this drone footage of the tree sit! There's also footage here of trees being felled in the snowstorm on Monday right up to the base of the sit.Currently, the only thing physically standing in the way of pipeline construction is the treesit on Peters Mountain. People in trees are doing what our "representatives" and "regulators" refuse to do — they're protecting land, water, and communities of Appalachia from corporations that believe their money gives them the right to pillage this land and pollute our water.Please donate to support pipeline resistance in Appalachia: bit.ly/SupportMVPResistance

Posted by Appalachians Against Pipelines on Tuesday, March 13, 2018

For updates from resistance to the Mountain Valley Pipeline, follow Appalachians Against Pipelines and Farmlands Fighting Pipelines on Facebook. To learn about some of the other pipeline fights mentioned here, follow No Bayou Bridge, Makwa Initiative, and Camp White Pine.

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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.

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