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In 2013, a fan asked 'Star Trek' to make Sulu gay. Here's his response to the news.

John Cho's recent announcement that Sulu will be gay in "Star Trek: Beyond" predictably set the Internet on fire.

Photo from "Star Trek: Beyond"/Paramount Pictures.


According to Cho, the decision was made, in part, as a tribute to George Takei, the openly gay actor and LGBT rights activist who played the character in the original series.

The actor revealed that Sulu's relationship with his partner — with whom he has a daughter — would be treated as any other relationship in the film and essentially be "no big deal."

Lots of fans were thrilled.



But the announcement about Sulu's sexual orientation had a surprise critic: Takei himself.

Photo by Frederick M. Brown/Getty Images.

"I’m delighted that there’s a gay character," Takei told The Hollywood Reporter. "Unfortunately, it’s a twisting of Gene [Roddenberry’s] creation, to which he put in so much thought. I think it’s really unfortunate."

Takei explained that he believed that while "Star Trek" is ready for a gay main cast member, the decision to depict Sulu's same-sex relationship in a prequel recasts the Enterprise helmsman as closeted in the original series.

Simon Pegg, who co-wrote the screenplay, responded in The Guardian to "respectfully disagree" with Takei.

Photo by Francois Nel/Getty Images.

"Justin Lin, Doug Jung and I loved the idea of it being someone we already knew because the audience have a pre-existing opinion of that character as a human being, unaffected by any prejudice," Pegg said in a statement.

"Their sexual orientation is just one of many personal aspects, not the defining characteristic."

One fan who was particularly excited by the news was Dan Wohl, a California graduate student who asked for exactly this move in a 2013 essay published on The Mary Sue.

"J.J. Abrams, if you’re listening, I think you should make Sulu gay," Wohl wrote.

Giving Sulu a same-sex partner, Wohl argued — and treating their relationship as simply something that is — would not only be a moving tribute to Takei's life and work, but help begin to correct "complicated but ultimately disappointing history" of mostly ignoring LGBT themes and characters on "Star Trek."

Wohl told Upworthy that he was delighted by the news.

Photo from "Star Trek: Beyond"/Paramount Pictures.

"I think it's awesome, and I'm really glad they're doing it," he said.

While he expected that the franchise would eventually introduce LGBT characters, he explained that he didn't believe the writers of the film would actually choose a character with such a long history to be the series' first.

"It's very rare to have something that you want so much to happen in your fandom come true."

"The normalization of things is really powerful," Wohl explained, praising the creators of "Beyond" for choosing not to make a grand statement about Sulu's sexuality within the film.

Making Sulu's sexual orientation just one more facet of a character with decades of rich backstory rather than a major plot point, he said, is just as powerful as using the character to make a big, sweeping statement.

"Almost just as important is to show that the things that were fought for should be viewed as just parts of life."

While he criticized the franchise for being behind the curve on LGBT issues to date, Wohl hopes that with a new series about to launch on CBS, "Star Trek" will further affirm its inclusive values.

"What I really think 'Star Trek' could and should become a pioneer in is when it comes to trans characters," he said.

Similarly, he said, if the franchise does introduce a trans character or characters, it could break new ground by refusing to make their gender identity the focus of their arc.

"The only time that you basically see a trans character is when the story is about them being trans."

But first, the franchise is — thankfully, finally — boldly going ... where many have gone before.

Photo by James Teterenko/Wikimedia Commons.

The show "was an attempt to say that humanity will reach maturity and wisdom on the day that it begins not just to tolerate, but take a special delight in differences in ideas and differences in life forms," creator Roddenberry wrote in an essay on the "Star Trek" philosophy.

While creators, actors, and fans may disagree about the particulars, with "Star Trek," what else is new?

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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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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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Molly was found tied to a tree by the new owners of the house.

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A Good Samaritan thwarts an attempted bank robbery.

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Michael Armus Sr., 69, was waiting in line when he noticed a man slip a teller a note. The tellers looked concerned, and the man who slipped the note had his shirt pulled over the bottom of his face. The man claimed that he had a gun. It was a robbery.

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