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Here's what actual trans military voices have to say about Trump's ban.

An estimated 15,000 trans people currently serve in the military.

In June 2016, the U.S. secretary of defense made a long-overdue announcement: The military was ending its ban on transgender service members.

With the 2011 end to the "Don't Ask, Don't Tell" policy banning gay, lesbian, and bisexual people from serving, allowing trans people to serve openly seemed like the logical next step.

As then-Secretary of Defense Ash Carter explained, “Our mission is to defend this country, and we don’t want barriers unrelated to a person’s qualifications to serve preventing us from recruiting or retaining the soldier, sailor, airman, or Marine who can best accomplish the mission.”


Fast-forward a year, and President Trump has undone that progress, tweeting that "the United States Government will not accept or allow transgender individuals to serve in any capacity in the U.S. military."

He cited "tremendous medical costs" as the reason behind his decision despite the fact that a RAND Corporation study found that the total additional cost of allowing trans people to serve in the military is $2.4 million-8.4 million. (For comparison, in 2014, the military spent more than 10 times that on erectile dysfunction medication alone.)

But maybe Trump's decision wasn't about cost at all. According to Axios reporter Jonathan Swan, a Trump administration official was quoted as saying the move "forces Democrats in Rust Belt states like Ohio, Michigan, and Wisconsin, to take complete ownership of this issue."

"How will the blue collar voters in these states respond when senators up for re-election in 2018 like Debbie Stabenow are forced to make their opposition to this a key plan of their campaigns?" Swan quoted the official as saying.

In other words, Trump's decision doesn't seem to be about readiness, cost, or any of the other reasons frequently tossed around by opponents of trans inclusion in the military. Instead, it's just a game of politics, with trans lives as pawns.

There are currently an estimated 15,000 trans people serving in the military. What do they think of Trump reinstating the ban? We asked them.

Amanda Clark was discharged back in 2007 after coming out as trans. While she says she's ambivalent about military service, she sees this as a matter of basic civil rights.

"I can’t possibly fathom what openly out trans people in the military are feeling right now. Hell, I feel scared now just being a trans person in the civilian world. It feels like the f*cking fascists who run this country are coming for us, and openly serving trans people are next. I’m sure a lot of officers/[non-commissioned officers] are going to be thrilled to get involved in paperwork hell discharging folks."

Kristen Carella, who served on active duty 2001-2005 as an intelligence analyst stationed in Germany, pointed out that many U.S. allies (18 in total, including Australia, Canada, France, Germany, Spain, and the United Kingdom) allow trans people to serve without issue.

"Here was an opportunity for this country to move forward, recognizing the sacrifices transgender people have ALWAYS made in the armed forces, by allowing us to serve openly. [According to Human Rights Campaign] stats 26% of the trans community serves in the military at some point during their lives, that is TWICE the rate of the general population.

Trump's decision is a stunning reversal that can be taken only as a slap in the face, personally to every transgender person who has ever served. It accomplishes nothing more than making sure transgender people remain a demonized and hated target that right-wing politicians can target to scare their base and push their agendas. Of course, all of this demonization ensures that the ignorant violence which leads bigots to murder transgender people in the streets (particularly trans women of color) will continue."

Penelope R., an intersex trans woman who served in the Air Force for six years before leaving to pursue transition, says "members are going to die" because of this new policy, and she urges those who might not generally support the military to care about this.

"[The] American military, despite its many infelicities, has always been a reliable space for many kinds of marginalized people to hide out in. This is why trans people are disproportionately represented in the military.

Enlisting was always a last resort for me — I've known I was trans since I was a child, and knew going into the military meant carving away parts of my identity I cherished, but at the time the alternative was death. Just death. I chose to live, and as a result I met my wife, found a chosen family that makes the sun rise for me, made enough money to afford transition, and qualified me to receive transitional health care from the Illinois VA. ... The military helped make my life worth living. And now it's all gone to shit for everyone.

Despite what he says, there's nothing Trump can say or do to stop trans people from serving — he can only get rid of those he knows about. It will only go back to how it was before, with trans service members confined to the closet at the risk of their careers."



Then-Defense Secretary Ash Carter lifts the ban on trans troops on June 30, 2016. Photo by Saul Loeb/AFP/Getty Images.

Landon Wilson, who served in the Navy and was the topic of a widely read 2014 Washington Post profile about trans people in the military, points out that the  ban means "honorably serving people" will be removed from service, "effectively weakening our country."

"It's a heartbreaking shame that the President of the United States is choosing to ignore the sacrifices of transgender service members, particularly at a time where so many have proven their dedication to this country. A diverse military makes a strong military; by removing honorably serving people from service, the President is effectively weakening our country, both as a fighting force and as a leader in civil rights."

Vivian Wise, an information systems technician on active duty in the Navy, came out to her shipmates the day President Obama and Secretary Carter lifted the ban in 2016. She disagrees with President Trump's assertion that trans people serving in the military is a "disruption."

"To say that my service has been a 'disruption' is an outright lie. My Commanding Officer, immediate superiors and co-workers have all been fully supportive of me. I am one of the senior technicians within my division, responsible for training our new sailors and managing our day-to-day and week-to-week work list. I was, until just now, being groomed to lead one of our division's two watch teams for our upcoming deployment, beginning late next year. In that capacity, I serve a critical role in my work center.

Summarily discharging me from military service, for nothing more than petty bigotry and electoral politics, is the disruption. The GOP as a whole, and the Trump administration in particular, are degrading my unit and hundreds if not thousands of other units across the armed services by taking away valuable people. We, and the American people, deserve better than this."

Cisgender allies, activists, and experts are voicing their concerns, as well.

In an email, TransMilitary co-director and executive producer Fiona Dawson (who, in 2015, documented the story of two trans service members who fell in love) weighed in on the move, saying she hopes Trump will actually take the time to meet some of the trans personnel he deems unfit for service.

"Donald Trump's assertions against transgender service members are baseless. Science and ethics determine there is no rational reason why the thousands of transgender women and men who have been defending our country and fighting for our freedom for hundreds of years should not be permitted to continue doing so."

Former Secretary Carter offered his opinion on the reinstatement of the discriminatory policy as well, saying that it "has no place in our military."

Advocacy organizations and civil rights groups across the country are issuing press releases, denouncing the tweet on a number of grounds.

The Palm Center called this "a worse version of 'Don't Ask Don't Tell'" and hit Trump over his claims of "tremendous costs."

"As we know from the sad history of that discredited policy, discrimination harms military readiness. This is a shocking and ignorant attack on our military and on transgender troops who have been serving honorably and effectively for the past year. As former Chairman of the Joint Chiefs of Staff Mike Mullen stated yesterday, their service must be respected. The Rand Corporation has estimated that the cost of medical care for transgender troops is approximately one one-hundredth of one percent of the military annual health care budget, or at most, $8.4 million per year. To claim otherwise is to lie about the data."

Tyler Deaton of the American Unity Fund, a conservative LGBTQ organization, criticized Trump for going back on what he saw as LGBTQ-friendly campaign promises in a statement that is long but worth reading in its entirety:

"President Trump promised to protect the transgender community. As President, he said he was 'respectful and supportive of LGBTQ rights' and would 'protect the community from violence and oppression.' But President Trump has broken his promise and, coupled with his administration's efforts to roll back protections for transgender students in our nation's public schools, he is developing an undeniable pattern of anti-gay and anti-transgender policy while in office. ... As conservatives and advocates for LGBTQ freedom, AUF calls on President Trump to reconsider his comments, and stand with all of our soldiers, including those who are transgender."

Former Justice Department official Vanita Gupta, currently president and CEO of the Leadership Conference on Civil and Human Rights, slammed Trump's move as "yet another broken promise to the American people."

"President Trump doesn't understand that our military is stronger when there are no discriminatory barriers to service. The civil and human rights community will continue to loudly and proudly stand up for the rights of all who are willing to protect the security of our country, including the thousands of transgender people currently serving in our military."

And of course, there was pushback from a number of Democratic and Republican politicians alike.

House Minority Leader Nancy Pelosi (D-California) commented on the sad irony of Trump's decision to increase discrimination on the 69th anniversary of President Truman's order to desegregate the military.

Sen. Kirsten Gillibrand (D-New York) announced plans to introduce legislation that would overrule Trump's decision.

Rep. Jerry Nadler (D-New York) highlighted the number of trans people serving in the military.

Rep. Illeana Ros-Lehtinen (R-Florida), who has a transgender son, spoke out against it as well.

Rep. Joe Kennedy III (D-Massachusetts) offered to stand in solidarity with trans soldiers.

Sen. Orrin Hatch (R-Utah) said "transgender people are people, and deserve the best we can do for them."

And Senate Minority Leader Chuck Schumer (D-New York) called trans service members "patriots."

Trans people exist in the world and have every right to engage in the same activities and occupations as anybody else.

This is a big deal, and it's not just a distraction. Nobody should be discriminated against for who they are — not in the military, not in education, not in housing, not in employment, not in health care, not at all.

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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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