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Identity

Here's how 18 people got over being homophobic, proving there's hope for everyone

"I looked for logical reasons to be and couldn't find any."

lgbtq, homopbobia, overcoming homophobia

Homophobia? Get over it.

There are many different reasons why some people are homophobic. A lot of them are raised in religious households where homosexuality is seen as sinful and they never get over their indoctrination.

A study from 2018 found that people who foster homophobic attitudes are less intelligent than those who accept people regardless of their sexuality. For the study, researchers asked subjects if they agree or disagree with the following statement: “Homosexual couples should have the same rights as heterosexual couples do.”

After comparing data sets, researchers found that the lower a person's cognitive intelligence, the more likely they are to be homophobic.

An older study from 2016 using an eye-tracking device found that some homophobic men seem to have an impulsive, automatic attraction to other men.

Homophobic attitudes are more prevalent in people with authoritarian personality types. Authoritarians have “submissive attitudes toward strong leaders, a desire to punish all who violate conventional moral codes, and strong fear that conventional morality is breaking down.”


There are also some who believe that humans evolved to be homophobic because it favors the propagation of the species. "In its simplest form, parents who showed a concern for their child’s sexual orientation may have left more descendants than those who were indifferent,” Gordon Gallup, a human sexuality researcher, wrote.

(It should be noted that Gallup formulated his theory in the ‘80s.)

Regardless of how people become homophobic, the good news is that Americans are slowly becoming more accepting of LGBTQ people. A Reddit user by the name of aestheticbear wanted to prove that everyone is capable of losing their homophobic views by asking the subforum, “What happened that made you stop being homophobic?”

According to the posts, growing up and meeting people who are LGBTQ was one of the most effective ways for people to get over their homophobia. It also helped when they got away from religious parents and began to see the world with their own eyes.

Here are 18 of the best ways that people got over being homophobic.

1. 

"I met some gay people. As it turns out they were just people." — moolord

2. 

"Not homophobic, but I woke up at about 10 when my mom said my uncle was banned from coming to our vacation condo by my father because he was gay. Before then I kind of let the arguments and both sides bit wash over me, but that was a crystalization point where I started noticing it as pure bigotry. I'm sorry the nicest dude in the family full of domestic violence and white-collar drug abusers cant come to Christmas because he's gay? You're both cheating on each other, sanctity of what marriage now?" — Robin_Games

3. 

"My mom slapped me and told me everyone has a right to be happy. That was in 9th grade 13 years ago." — Bloodllust

4. 

"Homophobia was the norm when I was growing up, then I got older and the political landscape changed which made me question my belief and I came to the conclusion it just didn't make any sense to be homophobic." — LuciferIsFallen

5. 

"I came out as gay." — pethal

6

"Realised that, fundamentally, being gay is just 'what' you are. It’s not 'who' you are." — Alternative-Rain-718

7. 

"I wasn't super homophobic, just a 'love the sinner, hate the sin' kind of guy. On my last day in high school, someone said 'Why do I care? They're not hurting me.' Cured me in three seconds. I still remember how magical that moment was for me." — Dirgonite

8. 

"Stopped listening to my homophobic family and left their religion. Oh and also realized I myself was pretty gay." — Raidden

9. 

"There are 20 years between myself and my youngest brother. I (and my SO) was raised in an explicitly homophobic/biphobic/transphobic fundamentalist religion (that I left with my SO in my early 20s) so I had a lot of internalized, conditioned, toxic beliefs about the LGBTQ that needed to be deconstructed. My little brother was obviously either gay or bi and it was obvious from the time he was six imho. He came out to my sisters, SO, and I as bi when he was 11 and we were like "tell us something we don't know lol." I think watching him just grow up, it was obvious that he hadn't chosen to be that way, it was just how he was. This false narrative that LGBTQ are somehow defective or sinners became more disgusting to me over time.

I can't remember exactly when it happened but my SO and I were like 'if our future child happened to be LGBTQ, could we teach that child the things we were taught about the LGBTQ?" We were like "no, that would be evil.'

Now, we have an 18yo niece that recently came out as a lesbian and we feel honored to be the only family that she trusts enough to introduce to her first GF. Spending time with her just reaffirms the fact that there is nothing wrong with the LGBTQ, it was our upbringing that was defective." — Jormungandr91

10. 

"I was in the military during the repeal of don’t ask don’t tell. I wasn’t pro-gay whatever that might mean but sitting in those mandatory command meetings really opened my eyes. There were some legit homophobes trying every trick in the book to justify everything from moving sleeping arrangements to outright violence out in the open with gay people in the room.

I may not have been super sympathetic before that but after I realized just how difficult it was for a gay person just to go to work. Or how many precautions they were taking on a daily basis to keep in the closet. It pushed me from disinterested in the subject to siding with the obviously pragmatic stance of pro-gay marriage and gays in the military." — Pencilowner

11. 

"Went off to college, started meeting gay people, quickly realized that their awesomeness was no different than any straight person’s awesomeness, stopped bothering to “otherize” them as I had in high school." — hailnaux

12. 

"I became good friends with someone who came out to me a year or so after we got to know each other. Turns out he wasn't the abomination that my Christian parents/church had taught me all gays were. Indoctrination of children is a bitch." — Vefantur

13. 

"Honestly I think it was Lady Gaga. I was young and impressionable and she was cool and so LGBT+ friendly that I just started accepting people. And then it turned out I was a lil gay too so things worked out well lol." — plutoforprez

14. 

"I grew up and met some openly gay people." — polkavert

15. 

"I became an atheist. Through a painful experience of getting through serious depression, I came out the other side with a different worldview. As soon as I shed religion I began to question a lot of things including how I really feel about LGBTQIA people vs what I'd been indoctrinated to believe. They are just people trying to go about their normal routine like myself. There's no vast conspiracy or 'gay agenda.'

Years later, I suspect I'm one of them now. I might be asexual but I'm not sure yet." —HonestSummer

16. 

"As a teen I loved to make fun/bash gay people and listen to heavy metal. Then one day Rob Halford from Judas Priest came out as gay. Well, he is fucking Rob Halford and he can do whatever the fuck he wants. He is Rob Halford and being gay did not make him any less amazing in my eyes. After that I stopped caring about people being gay or not. Who am I to second guess or mock Rob Halford's life choices?" — cambeiu

17.

"I looked for logical reasons to be and couldn't find any." — theyellowmeteor

18. 

"I grew up." — jthomas287

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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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