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Iraq War veteran shares how military service to his country prompted him to give up on Fox News

Iraq War veteran shares how military service to his country prompted him to give up on Fox News

Let me preface this post by saying that I am not a regular Fox News watcher. The handful of times I've tried to watch it, I haven't been able to stomach it for long. I don't watch televised news much anyway, but the blatant biases and sensationalist tone of Fox News is a huge turnoff for me.

It's not for a sizable percentage of Americans, though. There are more than a few people who believe Fox News when it says it's "fair and balanced." There are folks who believe Fox News when they tell them that "mainstream media" is hopelessly biased toward "the liberal left" and therefore can't be trusted like they can.

I wrote a whole article once about venturing over to Fox News's Facebook page to expose myself to different perspectives and coming away endlessly frustrated by the amount of verifiable falsehoods Fox News followers were perpetuating—a sad reality that only confirmed my belief that Fox News erodes people's ability to discern what is actually true.

But don't take my word for it. Take one of their analysts who quit the network and called it a "propaganda machine." Or take this veteran on Reddit who shared how they used to be an avid Fox News watcher until their tour in Iraq gave them a wake-up call.

In a Reddit thread about a Fox News segment discussing Fox News' coverage of Michelle Obama's DNC convention speech, user BabyMFBear wrote:


"My personal thoughts on Fox News:

Following 9/11, I found myself glued to Fox News. It was, after all, 'America's news network,' and included a 'no-spin zone' to ensure we were getting the real story. The reporting was 'fair and balanced,' and it was up to the viewer to come to conclusions based on 'we report; you decide.'

The hosts proudly wore their American flags on their lapels, and they taunted the French for not supporting our call to arms, and I cheered as we established the 'Coalition of the Willing' as we trounced Iraq, and started kicking Taliban ass in Afghanistan.

Then I got to Iraq, and my attitude changed. The Iraqis I worked with were normal, every day people. They were friendly and inviting. Aside from the language and cultural differences, they were no different than myself.

And then I met Colin Powell when he addressed everyone in the compound and, in not so many words, told us he appreciated our service but this mission was in error.

His exact words were 'You may hear a lot of things about the mission here in Iraq, but just know I am grateful for all of you who answered the call on behalf of your nation.'

That was quite a profound moment, not only for my time in service, but for my entire outlook on information, politics, and life in general.

Were Iraqi's better off without Saddam? Most likely. Looking back, that wasn't our problem to solve.

We have more weapons of mass destruction than nearly every other country combined, with the most advanced delivery systems available.

Could you imagine another country bombing us because our President isn't a good person with nuke release authority? Could you imagine being blown back into the Stone Age over it?

We are just living our lives, in total disagreement, in an intense atmosphere, but could you sit by peacefully while getting obliterated by a foreign country over it?

I'd be making homemade bombs to protect my family. I would want those invaders out of my country, even if it was because they and I both agree in our views of the U.S. President. That goes out the window when foreign troops are at my door.

Fox News helped sell a lie. Fox News put on theatrics, and pumped me up for war.

Two years later, I was covering a high-level NATO Security Conference. A 4-star Dutch general made the opening remarks about 'a war of necessity (Afghanistan)' and a 'war of choice (Iraq).'

I served in an unnecessary war. I am proud of my service to the Iraqi government. I was there to help. I am happy my next two deployments were in support of combat operations in Afghanistan.

Fox News sells theatrics. They sell hyperbole. That network's agenda is to serve the defense industry and military industrial complex.

Fox News has convinced people that someone like me hates America.

Fox News has convinced people that someone like me doesn't belong here.

Fox News has convinced people my views are unAmerican.

I'd be the first person to lead a charge against a foreign invasion.

Fox News has people convinced I'm the enemy.

Turn off Fox News. I'm pleading with you."

Comments have poured in, thanking the poster not only for their service, but for sharing their experience of breaking up with Fox News. Many of us have friends and relatives who are hopelessly glued to that station, constantly being fed the propaganda they're peddling, distrustful of award-winning journalism yet somehow trusting of Tucker Carlson.

Others shared similar stories of having once been Fox News fans but then recognizing it for what it was:

"I remember being a young man, watching Fox News after 9/11. It was shiny, entertaining, engrossing.

But I knew something was off about it. I didn't really know what Jingoism was, but I was sensing that this was most definitely some kind of propaganda.

I really do see the appeal and why it captures so many."Antnee83


"Brother, U.S. Army Signal Corp. Vet here, and I have to say a big Thanks, to you for being able to share your experience. I have also tried to share my experience from the perspective of a Signal Solder that is saturated with intel. as part of the job, and to witness the active misinformation campaigns that are used by the FOX propaganda outlets and how they were coordinated from the inside out, not to mention outside interference from hostile nations using 3rd wave warfare tactics against the U.S." – UrzasPunchline


"Iraq Vet here as well and the same for my wife (2004-2005) coming home I was a different person than when I went and not just for the obvious "going to war" reasons, but for the reasons you laid out above. If someone bombed my county to the Stone Age I'd be out there fighting them too, they're just supposed to lay down and let us run over them?!

I think there are a lot of Vets just like us but there are plenty of trump supporters too. I just hope this year is a wake up and the crazy things he's doing now will wake ppl up. I do know many trump supporters that say they can't vote for Biden and won't... but they also can't vote for trump so they'll stay home. That's good enough for me."Lathus01


I'd be making homemade bombs to protect my family

"Yep. Formerly in intelligence, and spent 2 years in Baghdad doing it. Lots of other intelligence people would refer to insurgents as "terrorists", and it always felt so wrong. They aren't terrorists, they are doing exactly what I would be doing if someone invaded my country and my city, and if you wouldn't you can't call yourself a patriot. Those people were basically fighting an army from the future and they STILL fought. Now THAT is bravery and patriotism."TalentKeyh0le


"Great post brother. I too was in the same boat as you. Born and raised in conservative catholic household and watched much of the same hyperbolic "America is great at kicking ass" propaganda generated by Fox News.

I too served in Iraq and in a very much "enemy" facing role where I spoke to these men we were holding indefinitely as enemy combatants and there were some long conversations I had with them where things sometimes didn't sit right, honestly.

I've had many years to realize what I was a part of, not necessarily regret, but certainly had to come to terms with things I did against men who were probably acting exactly as I would have in opposite roles.

I love this country and I love its people and still appreciate the time getting to serve it, but Jesus if I don't worry every day about what may be needed to save it's soul and that of all its citizens."TheRealAJ58


The original poster thanked people for the responses, saying "I hope what I've said here empowers other vets to speak out, and know they are not alone."

They also wrote of veteran suicides and the role false information plays:

"The number of veteran suicides is not hyperbole. Reconciliation is sometimes not possible without self-destructive behaviors. Some just cannot bring themselves to face their actions, and I cannot place blame on them. I place the blame on those who manipulate our youth into believing false realities."

I'm not saying we don't need a military. I fully believe in having national defense as a priority- right now more than at any other time since WWII.

We just need a military that is willing to defend our citizens, and not an away-team "bringing the fight to an enemy" under false pretenses.

Again, thank you. I'm now drained and emotional - in a good way.

I wish nothing but the best for all of us."

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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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