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An actual engineer explains why the wall is 'a disaster of numerous types waiting to happen.'

An actual engineer explains why the wall is 'a disaster of numerous types waiting to happen.'

Immigration arguments aside, what about the physical logistics of building Trump's wall along the border?

Many pundits, politicians, and ordinary people have offered their opinions on whether or not Trump's proposed border wall should be built. Most of the time, these discussions revolve around the philosophical and economic issues it raises, but what of the actual, physical building of the wall itself?

Enter Amy Patrick, real-life wall expert. In a now viral Facebook post, Patrick explained to those of us who don't design walls for a living why the planning and building of this wall is much more complicated and potentially much, much more expensive than most of us would ever guess.


Patrick first offered a list of her credentials:

"I’m a licensed structural and civil engineer with a MS in structural engineering from the top program in the nation," she wrote, "and over a decade of experience on high-performance projects, and particularly of cleaning up design disasters where the factors weren’t properly accounted for, and I’m an adjunct professor of structural analysis and design at UH-Downtown. I have previously been deposed as an expert witness in matters regarding proper construction of walls and the various factors associated therein, and my testimony has passed Daubert. Am I a wall expert? I am. I am literally a court-accepted expert on walls."

Well then. Here we go.

Wall expert Amy Patrick explains why the wall is "a disaster of numerous types waiting to happen."

"Structurally and civil engineering-wise, the border wall is not a feasible project," Patrick began. "Trump did not hire engineers to design the thing. He solicited bids from contractors, not engineers. This means it’s not been designed by professionals. It’s a disaster of numerous types waiting to happen."

Howdy.To recap: I’m a licensed structural and civil engineer with a MS in structural engineering from the top program...

Posted by Amy Patrick on Tuesday, January 8, 2019

What disasters, you may ask? Patrick explained:

"Off the top of my head...

1) It will mess with our ability to drain land in flash flooding. Anything impeding the ability of water to get where it needs to go (doesn’t matter if there are holes in the wall or whatever) is going to dramatically increase the risk of flooding.

2) Messes with all kind of stuff ecologically. For all other projects, we have to do an Environmental Site Assessment, which is arduous. They’re either planning to circumvent all this, or they haven’t accounted for it yet, because that’s part of the design process, and this thing hasn’t been designed.

3) The prototypes they came up with are nearly impossible to build or don’t actually do the job. This article explains more:

https://www.google.com/…/mobile.engineering.…/amp/17599.html"

Then she explained why the wall would be a logistical nightmare—and a lot more expensive than initial estimates.

"The estimates provided for the cost are arrived at unreasonably," Patrick wrote. "You can look for yourself at the two-year-old estimate that you see everyone citing.

http://fronterasdesk.org/…/Bernstein-%20The%20Trump%20Wall.…

It does not account for rework, complexities beyond the prototype design, factors to prevent flood and environmental hazard creation, engineering redesign... It’s going to be higher than $50bn. The contractors will hit the government with near CONSTANT change orders. 'Cost overrun' will be the name of the game. It will not be completed in Trump’s lifetime."

Well, that's some smelling salts right there. I know I hadn't taken any of those factors into consideration, and I'm not even a supporter of the wall.

"I’m a structural forensicist, which means I’m called in when things go wrong," Patrick continued. "This is a project that WILL go wrong. When projects go wrong, the original estimates are just *obliterated*. And when that happens, good luck getting it fixed, because there aren’t that many forensicists out there to right the ship, particularly not that are willing to work on a border wall project—a large quotient of us are immigrants, and besides, we can’t afford to bid on jobs that are this political. We’re small firms, and we’re already busy, and we don’t gamble our reputations on political footballs. So you’d end up with a revolving door of contractors making a giant, uncoordinated muddle of things, and it’d generally be a mess. Good money after bad. The GAO agrees with me."

(The GAO is the Governmental Accountability Office. Here's an article from The Hill detailing their report that the Trump administration has not taken all of the economic factors into account.)

Finally, she shared why the wall, even if built successfully, wouldn't be effective.

"I could, right now," Patrick wrote, "purchase a 32 foot extension ladder and weld a cheap custom saddle for the top of the proposed wall so that I can get over it. I don’t know who they talked to about the wall design and its efficacy, but it sure as heck wasn’t anybody with any engineering imagination."

Ouch.

"Another thing: we are not far from the day where inexpensive drones will be able to pick up and carry someone," she continued. "This will happen in the next ten years, and it’s folly to think that the coyotes who ferry people over the border won’t purchase or create them. They’re low enough, quiet enough, and small enough to quickly zip people over any wall we could build undetected with our current monitoring setup."

Seriously, though. Our technology is advancing so quickly, and in order to mitigate all of the possible breaches of the wall, we'd have to have border patrol agents set up along the entire border. And if we're going to do that, let's do that instead of the wall and save ourselves billions of extra dollars.

"Let’s have border security, by all means, but let’s be smart about it," Patrick concluded. "This is not smart. It’s not effective. It’s NOT cheap. The returns will be diminishing as technology advances, too. This is a ridiculous idea that will never be successfully executed and, as such, would be a monumental waste of money. 🤷🏻‍♀️"

Thanks for providing even more reasons the government shutdown over funding the wall is ridiculous, Ms. Patrick.

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

The American Kennel Club has crowned a new favorite.

via Pixabay

A sad-looking Labrador Retriever

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According to the American Kennel Club, for the past 31 years, the Labrador Retriever was America’s favorite dog, but it was eclipsed in 2022 by the Frenchie. The rankings are based on nearly 716,500 dogs newly registered in 2022, of which about 1 in 7 were Frenchies. Around 108,000 French Bulldogs were recorded in the U.S. in 2022, surpassing Labrador Retrievers by over 21,000.

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Photo by Ash Dowie on Unsplash

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America's Got Talent/Youtube

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