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15 'habits' of people who grew up with an 'emotionally fragile' parent

Having an emotionally fragile parent can leave lasting damage.

15 'habits' of people who grew up with an 'emotionally fragile' parent
via The Mighty

If you grew up with an "emotionally fragile" parent, chances are, you didn't have the typical, idyllic childhood you often see in movies.

Maybe your parent lived with debilitating depression that thrust you into the role of caregiver from a very young age.

Maybe your parent was always teetering on the edge of absolute rage, so you learned to tiptoe around them to avoid an explosion. Or maybe your parent went through a divorce or separation, and leaned on you for more emotional support than was appropriate to expect of a child.


Growing up with an emotionally fragile parent can leave lasting damage on a person as they leave childhood and enter adulthood.

Though it's true many kids who grow up with emotionally compromised or neglectful parents struggle with their mental health in adulthood, it's important to remember parents seldom set out to abuse their kids.

Oftentimes they simply do not have the support or resources to care for their own mental health. If you are a parent struggling with your mental health, we want you to know there is no shame in struggling, but it's important to seek the support you need.

Our partners at The Mighty wanted to know what "habits" people who grew up with emotionally fragile parents have now as adults, so they asked their community to community to share their experiences with us.

Here's are the "habits" our community shared with us:

1. Constantly Apologizing"

"Constantly apologizing is just one of many things I do as a result of an 'emotionally fragile' parent. Another is panic and, again, apologize if someone looks at their watch or checks the time when I am doing something, particularly if shopping. It is why I prefer to be alone and do things at my own pace, the anxiety and fear such an innocent thing like checking the time because of me is horrible." — Jodie B.

"Constantly apologizing for normal things like having an opinion and crying, bending over backwards to please everyone and keep the peace, not standing up for myself because when I did at home I'd get blown up at, etc." — Natalie J.

2. Overthinking

"I overthink everything all of the time because I'm trying to prepare myself for the next thing you will be disappointed in." — Faith L.

3. Always Feeling Afraid of Upsetting Others

"Not talking or doing anything for fear of getting into trouble or making people upset. Feeling like you can't move or speak without permission, even amongst your closet friends." — Rye B.

4. Having "Control Issues"

"I have huge control issues because I felt responsible for everyone's feelings. My father had a hairpin trigger temper and my mother was a perpetual victim, so I tried to micromanage every little thing to keep him from exploding, and protect her. Now I have debilitating anxiety and it becomes worse if I feel like something is out of my control. Because if I can't control everything, then something might upset someone, and it'll be my fault and not only will I be in trouble, but no one will love me. It's exhausting." — Murphy M.

5. Being a "Parent" for Others

"Be the mom for all my group friends. The mature person who will be there to give you the advice someone else can't." — Gladys M.

"Automatically parent everybody because I had to do it my whole life, but then I break down when it comes to trying to take care of myself." — Chloe L.

6. Struggling to Make Decisions

"I have a hard time making choices, or having an opinion. When you spent your whole childhood, teens and part of your 20s without the ability to choose things for yourself, you either feel guilty, or really uncomfortable having an opinion. Because you feel like you're going to get in trouble, or you're going to have a panic attack." — Kaylee L.

7. Ignoring Your Own Feelings

"I feel like I always have to fix everyone, take care of everyone, control everything. I feel like I have to ignore my feelings, and I have a hard time reaching out to people." — Kayla O.

"[I] try so hard to hide my feelings rather than rock the boat." — Jodi A.

8. Being a "People-Pleaser"

"I find it impossible to talk about how I feel. I constantly try make others happy, even if it means hurting myself. But I grew up with a dad who was both physically and emotionally abusive." — Jamie J.

"Being a people-pleaser. I do a lot of 'fawning' now because I always had to watch what I said in case it triggered either severe depression or anger." — Sela M.

9. Feeling Like You're a Supporting Role in Your Own Life

"I always feel like I'm just playing a small supporting role in the great drama of other people's lives instead of my life being a story of my own. I have a really hard time believing my feelings are valid and matter." — Susanna L.

10. Constantly Fearing Abandonment

"Constantly fearing abandonment… And no matter how much reassurance I get, I keep waiting for the moment where that love disappears." — Monika S.

11. Overanalyzing the Behavior of Others

"I overanalyze how people talk and their body language. When you're used to looking for small clues to try to make life easier or prepare for a meltdown, it's… a hard habit to break." — Lexi R.

12. Pushing People Away

"I push people away when I hit my depression low since that's what my mom did. I'm trying to learn how to let people in but it's hard to do at times and I never know how to tell people." — Jennifer B.

13. Getting Offended Easily

"My daughter would say I cry too much and get offended too easily, and she isn't wrong." — Kat E.

14. Cleaning Up After Others

"Cleaning other people's homes while you're there because you grew up cleaning up after everyone because your parents didn't clean." — Des S.

15. Being Very Empathetic

"Yes there has been some negative impact but I also recognize that I learned how to be empathetic at a really young age. I remember my mom crying — I was only about 3 years old — and I went and got her the stuffed bear she had in her room." — Lauren A.

If you grew up having to take care of an emotionally fragile parent, you're not alone. Whether you're struggling to assert boundaries in your life, have trouble communicating your needs or don't know how to take care of yourself, we want you to know there's a community of people who want to support you in your recovery journey.

The article was originally published by our partners at the Mighty and was written by Juliette Virzi.

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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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