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This guide to weight and body image from the Girl Scouts is freaking amazing.

A quick and simple look at fighting negative body image.

body image, Girl Scouts, fat shaming
Image pulled from YouTube video

Girl Scouts share social media posts on positive body image.

This article originally appeared on 06.19.17


The Girl Scouts' guide to help parents talk to their daughters about weight and body image is kind of amazing.


The guide, titled "Yes, Your Daughter Just Called Herself Fat," written by Girl Scouts’ developmental psychologist, Andrea Bastiani Archibald, includes a step-by-step look at responding to your child should they come home one day from school saying, "I'm fat."

First of all, it breaks down just how prevalent fat-shaming is in our culture:

"According to studies, a whopping 80 percent of 10-year-olds are afraid of being fat. Why? Because they’re constantly surrounded by both subtle and direct messages that curvier or heavier girls aren’t as well liked, aren’t as likely to succeed in business, and in general, aren’t going to have as much fun or happiness in their lives."

Second of all, it explains why the knee-jerk response "You're not fat. You're beautiful!" that so many of us have actually isn't helpful.

Honestly, this part is so good that I'm just going to include the whole thing (which in its own awesome way, features the only reference to "The Dress" that won't make you want to scream):

"[I]f she really sees her body in a certain way, simply telling her to stop seeing it that way isn’t going to help much. Remember that infamous dress on social media a few years back that some people thought was blue and some thought was gold—and how frustrating it was when those who saw it differently insisted that you were seeing it wrong and tried to get you to see it their way? That’s kind of how your girl is going to feel when you tell her that her body simply isn’t the way she thinks it is.
...by essentially telling her that she's not fat, she's pretty, you're reinforcing the idea that fatter, rounder, curvier or heavier bodies aren't beautiful — which simply isn't true. There are endless ways to be beautiful, and your daughter will grow up with a much healthier relationship to her body if you teach her that in a genuine way from a young age."

This is such an important message that we don't hear often enough. Calling someone fat isn't bad because being fat is inherently bad, but it is bad to call someone fat as an insult because it implies that there's something wrong with larger bodies.

Fat is just another type of body, andall types of bodies are OK.

The guide also features some great steps parents can take if their daughters feel negatively about their body fat.

1. Don't assume you know where she's coming from.

"A better approach is to pause for a moment and ask your daughter why she thinks she’s fat," the guide advises. "Is it because her clothes are fitting differently than they used to or that a size she used to wear doesn’t feel comfortable anymore?"

Maybe her discomfort has to do more with the bodies of her classmates or what she's seeing in the media. Or maybe she is fat, and really just needs you to tell her that's OK too. Getting to the root of what's causing body image issues is an important first step.

Again, the guide warns against those knee-jerk reactions: "If she says she thinks her legs are bigger or her tummy is rounder than those of her friends, those may actually be correct observations — and there’s nothing wrong with acknowledging that."

2. Set a good example for her!

Kids pick things up from their parents all the time and internalize those messages even if parents aren't trying to pass them on. This is just as much about setting a good example as anything else.

"Another reason your girl might call herself fat is because she’s heard you do the same to yourself," reads the guide. "Your daughter listens to everything you say — and if you’re picking yourself apart in front of the mirror or complaining about your weight, there’s a good chance that she’ll follow in your self-disparaging footsteps."

That means giving yourself a bit of a break too. Just as you don't want her to have to try to live up to unrealistic beauty standards, remind yourself that you don't have to either.

"Identify parts of your body that serve you well and make note of the things you really do love about the way you look," says the guide. "Healthy habits like eating right and exercise are good for everyone and should be a daily part of your routine, but fixating on your body and how it could or should be different isn’t healthy for anyone."

3. Pay attention to the kind of media she's consuming and make sure she's seeing a variety of body types being celebrated.

TV, movies, and advertising are chock-full of messages meant to instill shame around body appearance, especially in girls and women. A bit of emotional counterprograming can go a long way. For example, check out the upcoming children's book "Glitter Stripes"; and for older girls, Hulu's "My Mad Fat Diary," Melissa McCarthy's performance in "Ghostbusters," and Chrissie Metz in "This Is Us," and Lynn Champlin on "My Crazy Ex-Girlfriend" are great body-positive/fat-positive representations in the media.

Video of plus-size blogger posted on Girl Scouts Twitter page below:

The guide advises parents to "go the extra mile to compensate for some of the less-healthy messages your daughter may be getting from other sources" by exposing them to accomplished women of all shapes and sizes.

"She needs to know you don’t have to be a certain size or shape to make it big in life."

This guide is just one of the many phenomenal parenting resources you can find on the Girl Scouts website.

Other topics include how to raise your children to be leaders, how to stand up to bullying, and how to be the best they can be in school. They're all great in their own ways, but the body image article stands out especially.

Thanks to the Girl Scouts, parents can now feel equipped to handle this potentially difficult conversation.

Sponsored

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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