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27 progressive Twitter users worth following for a deeper look at a few familiar topics.

Looking for a more 'social' social network? Give these recommendations a try.

Twitter can be a huge waste of time — unless you're following the right people.

To mix things up, I try to follow new people at every available chance. Finding new voices and views to follow, however, can be challenging. After all, Twitter's "Who to Follow" section can feel a little stale at times. So if, like me, you're on the lookout for some fresh perspectives, here's a short list of some of the people who make my own Twitter feed fun and informative.

1. Sara Benincasa — @SaraJBenincasa

Author and comedian Sara Benincasa is your go-to Twitter account for lighthearted takes on current events, measured opinions on serious matters, and more than a few laughs. Her latest book, "DC Trip," came out late last year, and her next, "Real Artists Have Day Jobs," is due this April.


2. Jane Doe, MD — @DrJaneChi

Jane is a physician (who happens to also provide abortions), an intersectional feminist, and lover of small, furry animals. There's almost certainly something important happening in the world you don't know about that Jane is tweeting about right now.

3. Robin — @caulkthewagon

Robin is a Bostonian who spent much of last year organizing around the #NoBoston2024 cause, fighting the city's bid to host the 2024 Olympics. She tweets about labor, organizing, and a variety of progressive causes.

4. Melissa Gira Grant — @melissagira

Journalist Melissa Gira Grant is the author of "Playing the Whore: The Work of Sex Work." She writes on sexual politics, technology, and workers' rights.


5. Imani Gandy — @AngryBlackLady

Imani is the senior legal analyst over at RH Reality Check. Her tweets on race, gender, and pop culture are supplemented by some really great, insightful articles.

6. Andrea Grimes — @andreagrimes

Andrea is a digital editor at the Texas Observer. She's passionate about reproductive health, and she's absolutely hilarious on Twitter. In response to the "ice bucket challenge," Andrea launched the "taco or beer challenge," in which you eat a taco and/or drink a beer, and donate to help fund abortion. Because hey, why not, right?


7. Michelle Kinsey Bruns — @ClinicEscort

As her handle indicates, she's an escort for patients in and out of abortion clinics, helping to shield them from anti-choice protesters. Michelle's series of tweets about clinic violence using the #is100enough hashtag went viral late last year after the shooting at the Colorado Springs Planned Parenthood.


8. Katie Klabusich — @katie_speak

Katie is a writer and host of "The Katie Speak Show" on Netroots Radio. She's a fierce advocate for abortion rights and bodily autonomy and is just an all-around solid choice to follow on Twitter. Last year, she was featured in an Upworthy story about abortion stigma.

9. Chris Mosier — @TheChrisMosier

Chris is an athlete and the first transgender member of Team USA. He's the executive director of GO! Athletes, a nonprofit for current and former LGBTQ high school and college athletes.

10. Molly Knefel — @mollyknefel

Molly is a journalist, writer, and co-host of the "Radio Dispatch" podcast. She's also an after-school teacher for grades K-8. She's a great follow for anyone interested in hearing a fresh take on current events.

11. Jessica Luther — @scATX

Jessica is an Austin, Texas-based independent journalist and sportswriter. She's done some truly impressive work on the topic of sexual assault within college athletic programs.


12. Carlos Maza — @gaywonk

Carlos is a research fellow at Media Matters for America. Until recently, his work focused primarily on LGBT rights, but it has since expanded to include a wide range of progressive causes.


13. Jamie Kilstein — @jamiekilstein

Jamie is a musician and comedian. He's the co-author of "#Newsfail" and co-host of the "Citizen Radio" podcast. Last year, Jamie was featured in an Upworthy article about catcalls not being compliments.

14. Ijeoma Oluo — @IjeomaOluo

Ijeoma is a Seattle-based writer and editor-at-large at The Establishment, a multimedia company founded, funded, and run by women. She's a great follow for smart takes on the intersection of feminism, race, pop culture, and parenting.


15. Pasta — @pastachips

Pasta is an Edinburgh, Scotland-based sex worker who writes and blogs about politics, labor, police violence, stigma, and other issues.


16. Monica Roberts — @TransGriot

Monica is a Houston-based blogger and civil rights activist. She's won multiple awards for her blog TransGriot, and in 2013, she was named to the inaugural Trans 100 list.

17. Chris Geidner — @chrisgeidner

Chris is the legal editor over at BuzzFeed News. In the past, he's done some truly phenomenal writing on LGBTQ issues, but lately he's been churning out some truly informative posts about the death penalty and the Supreme Court's role in its future.

18. Cameron Russell — @CameronCRussell

Cameron is a model, writer, editor, and climate activist. In 2012, she gave a TED Talk about appearance and the privilege that comes along with winning a genetic lottery. In 2013, she founded Space Made, an artist collective based in Brooklyn. Her tweets tackle issues of gender, race, and climate.


19. Linda Sarsour — @lsarsour

Linda is a racial justice and civil rights activist and media commentator. She's a Palestinian-American and Muslim. Her informative tweets give a fresh look at what sadly remains a very relevant issue: Islamophobia around the world.

20. Zoé S. — @ztsamudzi

If you're interested in issues surrounding race and gender, then Zoé is a must-follow. She's blunt, unapologetic, and so frequently just spot-on in her observations.


21. Chase Strangio — @chasestrangio

Chase is a staff attorney at the ACLU, working with its LGBT & AIDS Project. He's a great follow for anyone interested in learning a bit about some of the struggles facing trans and gender-nonconforming people when it comes to the police.


22. Cyd Zeigler — @CydZeigler

Cyd is the co-founder of Outsports.com, a website dedicated to covering LGBT athletes. With some of the first athletes in major sports coming out as LGBT in recent years, Cyd's work has been essential reading as we watch these early pioneers make history.

23. Leah Torres, MD — @LeahNTorres

Leah is an OB-GYN who, yes, provides abortions. She's an advocate for her patients and is a proponent of comprehensive sex education.

24. Tina Vasquez — @TheTinaVasquez

Tina is an immigration reporting fellow at RH Reality Check. On Twitter, she shares her eye-opening opinions on race and gender and is most certainly worth a follow.

25. Ian Thompson — @IantDC

Ian is a legislative representative at the ACLU. He works on issues ranging from LGBT rights to sex education. Prior to working at the ACLU, he was an intern in Rep. Dennis Kucinich's D.C. office.

26. Dave Zirin — @EdgeofSports

Dave is the sports editor at The Nation. He hosts the "Edge of Sports Radio" podcast, and his work rides the line between sports and politics, giving him a unique perspective. He's the author of eight books.

27. Upworthy — @Upworthy

OK, OK, I work for Upworthy, so of course I'm going to recommend you follow us. But have you seen our live-tweets of award shows and debates? Or how about one of our UpChats? They're super fun and informative. And as a bonus, you get all our fun articles delivered right to your Twitter feed.

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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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