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Joy

10 photos of seriously wounded vets remind us about the real costs of war.

Their wounds belong to all of us.

democracy, justice, wounded veterans, documentation, portraits
Image by David Jay/ David Jay Photography.

Maj, Matt Smith at Walter Reed Medical Center in Bethesda, Maryland.

This article originally appeared on 05.31.15


Photographer David Jay specializes in fashion and beauty, stuff that's "beautiful and sexy — and completely untrue," as he puts it. But that's not all he photographs.

Three years ago, Jay began to take pictures of young, severely wounded soldiers returning home from the wars in Iraq and Afghanistan.

Trigger warning: These portraits don't shy away from wounded bodies.


Be prepared. I found them shocking at first. But keep looking. The more I looked, the more beauty and humanity I found reflected here. (The photo captions are from the Jay's Unknown Soldier Project Facebook page. All images used with permission.)

military, body image, disabilities

Lt. Nicholas John Vogt, U.S. Army

Image by David Jay/ David Jay Photography.

This is 1st Lt. Nicholas John Vogt, U.S. Army. On Nov. 12, 2011, he was severely injured by an IED while on a foot-patrol in Panjwaii, Afghanistan. We took these pictures this past weekend in the swimming pool at Walter Reed Medical Center. I asked Nicholas for his permission to post these images and this was his response: "The only thing that I want to pass on is this: Losing limbs is like losing a good friend. We wish we could still be with them, but it wasn't 'in the cards.' Then we get up, remember the good times, and thank God for whatever we have left." Image by David Jay/ David Jay Photography. All images used with permission.

In a National Public Radio interview about his project, Jay said, "You can imagine how many times each of these men and women have heard a parent tell their child, 'Don't look. Don't stare at him. That's rude.'"

"I take these pictures so that we can look; we can see what we're not supposed to see. And we need to see them because we created them." — David Jay
photography, mental health, veteran rights

Taking a swim.

Image by David Jay/ David Jay Photography.

Jay wants us to see, to become even a little familiar with the tragic loss of limbs and burned skin of wounded vets — his portraits are 4 feet wide — but he also wants us to see them as people and to think about their experiences and those of people in their lives.

health, David Jay, The Unknown Soldier

Bobby Bernier with daughter Layla.

Image by David Jay/ David Jay Photography.

This past week, I went to San Antonio, Texas. There I had the privilege of photographing both Daniel Burgess and Bobby Bernier. They are friends. Daniel stepped on a IED, losing one leg and destroying the other. Bobby was hit by incoming artillery, sustaining burns over 60% of his body. He is pictured here with his daughter Layla.

IED, Maj. Matt Smith, Afghanistan

Maj, Matt Smith at Walter Reed Medical Center in Bethesda, Maryland.

Image by David Jay/ David Jay Photography.

This is Maj. Matt Smith. This past week, Matt allowed me to photograph him in his room at the Walter Reed Medical Center in Bethesda, Maryland. Less than three months ago, on June 8, 2013, in Paktika province, Afghanistan, Matt was shot along with five others by a member of the Afghan National Army. The bullet severed his femoral artery, resulting in the amputation of his leg. A private and soulful man, it was an honor to photograph him. Thank you, Maj. Smith.

disabled, war, amputee

Spc. Marissa Stock injured by an IED.

Image by David Jay/David Jay Photography.

burn victim, roadside bomb, survivor

Jerral Hancock survived a roadside bomb.

Image by David Jay/ David Jay Photography.

This is Jerral Hancock. He was driving a tank in Iraq. A roadside bomb pierced the armor, breaching the interior. We shot these pics two weeks ago at his home in Lancaster, California, where Jarral lives with his two beautiful children. We ended up hanging out into the night, smokin' ciggys ... so I kept taking pictures.

"To the men and women of The Unknown Soldier, I can't thank you enough for your courage and sacrifice ... both on and off the battlefield. It is an honor to photograph you." — David Jay
swimming, photography, internal injuries, Airborne Ranger

SFC Cedric King floats in the pool.

Image by David Jay/David Jay Photography.

On July 25, 2012, SFC Cedric King, an Airborne Ranger, was severely injured by an IED while serving his country in Afghanistan. Due to the explosion, Cedric sustained a multitude of internal and external injuries, losing both his legs. Cedric was doing his laps while I was photographing 1st Lt. Nicholas Vogt in the pool at Walter Reed Medical Center last week. Cedric kept watching, so I had to ask. Cedric said, “That man (Nicholas) doesn't know it, but he changed my life. There was a point when I was so down that I thought I couldn't go on. And then one day I saw him swimming ... and I just thought, wow ... if he can go on like that, then I can go on too." Cedric will also change people's lives. Already has.

Marine, foot-patrol, Afghan Army

Michael Fox, 27-year-old Marine.

Image by David Jay/David Jay Photography.

This is Michael Fox, a 27-year-old Marine and an amazing man. On Nov. 15, 2011, Michael was on foot-patrol in the Helmand province of Afghanistan. His is the first picture of "The Unknown Soldier."

The SCAR Project, battle-scarred, therapy

Staff Sgt. Shilo Harris in Houston, Texas.

Image by David Jay/David Jay Photography.

This past weekend, I photographed Staff Sgt. Shilo Harris in Houston, Texas. He came up from San Antonio to see one of my other exhibitions, The SCAR Project (www.thescarproject.org). Shilo was severely burned on Feb. 19, 2007, by a roadside bomb estimated at 700 pounds. He lost three men out of a crew of five. Only Shilo and his driver survived the blast. Shilo has a book coming out soon. He is truly an amazing man, and I am honored to call him a friend.

"The Unknown Soldier is about neither war or politics ... but rather something infinitely simpler and more powerful." — David Jay
healing, medicine, remedy, hope

Thomas Young in Kansas City, MO.

Image by David Jay/ David Jay Photography.

The Library of Congress has acquired images from Jay's The Unknown Soldier project as part of its documentation of the wars in Iraq and Afghanistan. This speaks to the power of these images in capturing war's aftermath. But they are so much more than documentation.

Pictures like these help those of us who remain at home to begin to comprehend the true human cost of war.

Sponsored

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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via Pixabay

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Photo by Ash Dowie on Unsplash

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America's Got Talent/Youtube

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