+
More

A woman who's tackling revenge porn, and 9 other women changing the world for the better.

True
L'Oréal Paris Women of Worth

Despite facing numerous social and political obstacles throughout history, women have always been powerful agents of change.

Every era has its heroines — women who inspire, empower, and offer the world an extra dose of awesome. Some of these women are household names, while others fly under the radar, improving their communities and impacting people around them with little fanfare or fame.

Those unsung female heroes are who L’Oréal Paris had in mind when they created the philanthropic program, Women of Worth. Every year for the past 12 years, 10 women have been chosen from thousands of nominees to be honored for their selfless volunteer work as advocates and founders of charitable causes.


For 2018, the list of nominees is impressive. Of these 10 women, one will be chosen (by you, if you vote before the end of November) as a National Honoree and receive an additional $25,000 for her organization.

Get ready, because reading about these extraordinary women will make you want stand up and cheer.

In 2014, Shreya Mantha was tutoring sex-trafficking survivors to help them get their GEDs. Then she started her own foundation — at age 13.

Shreya Mantha. All photos via L’Oréal Paris.

Shreya is now 17 and her Foundation for Girls is a thriving, youth-led social venture hoping to change the life-trajectory of at-risk girls and youth in Charlotte, North Carolina. Through a network of “caring coaches” and programs in digital literacy, financial wellness, leadership, and health and wellbeing, teen moms, homeless girls, refugees and trafficking survivors receive the skills and structured support they need to realize their full potential and take charge of their futures.

As of June 2018, Foundation for Girls has reached 1,480 girls and youth, has almost 300 workshops and completed more than 14,000 hours of life-changing investment.

Adding to the “Wow, these kids!” factor, Alisha Zhao was 17 when she founded Kids First Project to help homeless kids achieve their dreams.

Alisha Zhao

When she was 14, Alisha volunteered at a homeless shelter, and it struck her how all of the kids there had big dreams and ambitions, but limited opportunities. A few years later, in 2015, Kids First Project was born. The initiative helps bridge the gap between homeless kids and the resources they need to reach their full potential.  

Today, the Kids First Project is in 10 locations with more than 400 volunteers in the Portland and San Francisco Bay areas — serving approximately 500 families who are experiencing homelessness each year. The now 20-year-old says her goal is to "work on the issue of youth homelessness and human rights for my entire life," and that this honor will help her "empower children experiencing homelessness to reach their full potential and help break the generational cycle of poverty."

Meanwhile, 25-year-old Hannah Dehradunwala is tackling food waste in New York with her platform Transfernation.

Hannah Dehradunwala (right).

Where Hannah grew up in Pakistan, no one let food go to waste. But when she returned to the United States to attend NYU, she was struck by the amount of food that got thrown out after catered events on campus. So she created Transfernation, a platform for companies and corporate hospitality groups to donate extra food to those in need of food assistance.

By coordinating ride-share drivers and bike messengers to pick up leftover catering and deliver it to community based organizations, the organization is helping empower businesses to reduce their environmental footprint and decrease food waste. So far, Transfernation has rescued 530,000 pounds of food and provided 510,000 meals to those without reliable access to food sources.

Veteran Genevieve Chase was severely injured in the line of duty. Now she’s channeling that experience into helping other female veterans.

Genevieve Chase

While deployed in Afghanistan as an Intelligence Soldier with the Army Reserve, a car filled with explosives plowed into Genevieve Chase’s truck, leaving her with external wounds and a traumatic brain injury. What's more, when she came home, like so many other soldiers, Genevieve suffered from PTSD and struggled with depression and suicidal ideation.

And as she dove into veteran advocacy, she felt the absence of awareness and support for female veterans. So she attempted to fill that void by starting the non-profit organization American Women Veterans, which honors and empowers military women, veterans and their families. The 40-year-old’s goal is to create “a community of empowered and inspiring women who will continue to ensure that all military women and veterans get the care and benefits we’ve earned so we can continue service to our communities both in and out of uniform.”

Holly Jacobs is helping victims of another form of trauma —nonconsensual porn — with her Cyber Civil Rights Initiative.

In 2011, Holly was blindsided when nude photographs she’d shared privately with a romantic partner showed up on the internet without her consent. Her identity was exposed, and she felt like running from the world. Instead, she decided to fight back — for herself and other victims of “revenge porn.”

Holly Jacobs

Today, the 35-year-old’s Cyber Civil Rights Initiative (CCRI) serves thousands of victims around the world. Advocating for technological, social, and legal innovation to fight online abuse and discrimination, CCRI has helped advise legislation in 30 states, Washington, D.C. and the federal government. And the CCRI Crisis Helpline serves hundreds of callers per month. “Nonconsensual pornography is intended to make women feel worthless,” Holly says. "I want to tell victims like myself that they don’t have to run or hide in shame. They are not alone, and together we have the power to speak up and fight online abuse.”

Chicago police officer Jennifer Maddox fights crime by providing after school programs for at-risk kids.

Jennifer was a single mother working two jobs when she founded Future Ties, an after-school program that provides a haven for young people in the Chicago's Woodlawn area. She had noticed that most crime and gang activity took place after school, so in 2009 she set out to give kids a productive, empowering "safe space" where kids go instead — using her own money to purchase supplies.

Jennifer Maddox

Today, Future Ties serves about 40 elementary students, with adult volunteers, parents, and young people from the community serving as role models and tutors. Since its founding, gang-related activities have declined and crime has decreased by 50 percent. Jennifer, now 47, wants to expand Future Ties' life-changing services to help the 1,200 young people living in her community.

Laura Reiss, 49, also started an after school program, encouraging kids to be kind and contribute to their world.

Laura's foundation started out as a free after-school kindness program at her children's elementary school in Boca Raton, Florida. That single club morphed into The Samaritans365 Foundation, Inc., a not-for-profit organization that teaches kids to be kind to themselves and others, and make a positive impact in their communities and the world.

Laura Reiss

The Samaritans365 Foundation, Inc. now has more than 400 ambassadors and 4,050 members in 90 chapters across nine states. All together, they have collected and distributed $1,347,000 in goods, raised $2.5 million in disaster relief, and invested 613,213 community service hours. Laura's strong formula for empowering people is helping her reach her goal of "leaving this world better for having been here."

Christy Silva took a parent's worst nightmare and turned it into a life-saving screening program.

In 2010, Christy's seven-year-old son Aidan collapsed without warning and died of Sudden Cardiac Arrest. They had no idea he had a heart condition, and despite investigations, the cause of the arrhythmia that led to the heart attack is still unknown. Then Christy learned 70 percent of conditions that cause SCA in kids can be detected by a simple, non-invasive EKG (electrocardiogram). She decided she had to help other families avoid the same fate.

Christy Silva

Thus was born Aidan's Heart Foundation, which provides awareness, education, support and coordinated screening efforts. Through screenings of 1,800 youth in Pennsylvania, the Foundation has detected previously undiagnosed and potentially life-threatening heart conditions in 25 young people. It's also helped pass legislation to equip schools with updated defibrillator (AED) devices and trained more than 4,500 sixth-grade students and 400+ adults in life-saving CPR-AED skills. Christy, 44, says "Aidan may be gone, but our work is keeping his legacy alive.”

Betty Mohlenbrock proves it's never too late to make a difference with her nonprofit reading program for incarcerated parents.

Betty is a retired classroom teacher who has always been committed to improving kids' lives. In 2010, at age 70, she came out of retirement to found Reading Legacies, a nonprofit dedicated to negating some of the devastating effects of incarceration on families by fostering relationships between incarcerated parents and their kids through the simple act of reading aloud together.

Betty Mohlenbrock

Last year, Reading Legacies facilitated 8,000 read-aloud experiences among family members participating in its programs. Based on research the org's conducted, 73 percent of children enjoy reading more and nearly 70 percent communicate more with their parents since starting the program. Every teen who has volunteered with Reading Legacies says it has strengthened their leadership skills, and 94 percent of incarcerated parents participating have felt a boost in morale and feel more connected to their children at home.

Betty, now 78, wants "to give people hope, especially if they haven’t had a reason to be hopeful for a long time.”

As a two-time cancer survivor, Carolyn Keller understands how important a wig can be for women undergoing chemo.

Carolyn was diagnosed with cancer in 2002 and again in 2005. When she lost her hair while undergoing chemotherapy, she started using wigs to cover her hairless head. Then, when her sisters-in-law were diagnosed with cancer, she passed her wigs onto them. Carolyn felt how empowering it was as a survivor to pass on wigs to another woman going through cancer treatment. As Carolyn, now 57, says, "Sometimes simple gestures can be the most healing."

Carolyn Keller

That's why she founded EBeauty Community, Inc. Through the organization's Wig Exchange Program, more than 25,000 women have received and donated wigs, and 10,000 wigs are distributed each year to women across the country through a network of hospital partners. EBeauty is considered the largest wig exchange program for women undergoing treatment for cancer in the country. And so far, Carolyn's goal "to help women embrace their identity and dignity when everything else in their life feels out of control” seems to be right on target.

Does one of these women's stories stand out to you? You can offer her your vote.

Throughout the first three weeks of November, anyone can cast a vote to choose this year's Women of Worth National Honoree. If you'd like to help one of these women receive an additional $25,000 for her cause, go to the L'oréal Paris website, and vote before November 30th, 2018.

Good luck choosing just one, though. They all deserve all the kudos.

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.

Joy

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

The sweet-faced, loveable Labrador Retriever is no longer America’s favorite dog breed. The breed best known for having a heart of gold has been replaced by the smaller, more urban-friendly French Bulldog.

According to the American Kennel Club, for the past 31 years, the Labrador Retriever was America’s favorite dog, but it was eclipsed in 2022 by the Frenchie. The rankings are based on nearly 716,500 dogs newly registered in 2022, of which about 1 in 7 were Frenchies. Around 108,000 French Bulldogs were recorded in the U.S. in 2022, surpassing Labrador Retrievers by over 21,000.

Keep ReadingShow less
Pop Culture

Melissa McCarthy describes Halle Bailey’s endearing habit on ‘The Little Mermaid’ set

Even the guy holding the boom mic said it was his “favorite thing.”

Melissa McCarthy shares Halle Bailey's "divine" habit.

Music can truly feel like magic sometimes, especially when someone has the voice of an angel—or perhaps a wistful, land-loving mermaid.

Reviews of Halle Bailey's performance in Disney's new live-action "The Little Mermaid" have been overwhelmingly positive, which isn't too surprising considering her vocal talents. But according to co-start Melissa McCarthy, who plays the wicked sea witch Ursula in the film, Bailey's siren-like appeal didn't end when the cameras stopped rolling.

In a press interview for the movie, McCarthy shared that Bailey had an endearing habit of quietly humming all the time, sometimes without even realizing that she was doing it. McCarthy's description of the way she and even members of the sound crew reacted to Bailey's constant lovely humming is a testament to the heartwarming, wholesome magic of music.

Keep ReadingShow less
@geaux75/TikTok

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

Molly, an adorable, affectionate 10-year-old pit bull, found herself tied to a tree after her owners had abandoned her.

According to The Dodo, Molly had “always been a loyal dog, but, unfortunately, her first family couldn’t reciprocate that same love back,” and so when the house was sold, neither Molly nor the family’s cat was chosen to move with them. While the cat was allowed to free roam outside, all Molly could do was sit and wait. Alone.

Luckily, the young couple that bought the house agreed to take the animals in as part of their closing agreement, and as soon as the papers were signed, they rushed over to check in.
Keep ReadingShow less

A woman is upset with her husband and wants to leave him.

There are a few big reasons why 70% of divorces in the United States among heterosexual couples are filed by women. Women have more economic opportunities than in decades past and are better positioned to care for themselves and their children without a husband’s income.

Another big reason is that even though the world has become much more egalitarian than in the past, women still bear the brunt of most of the emotional labor in the home. Gilza Fort-Martinez, a Florida, US-based licensed couples’ therapist, told the BBC that men are socialized to have lower emotional intelligence than women, leaving their wives to do most of the emotional labor.

Secondly, studies show that women still do most of the domestic work in the home, so many are pulling double duty for their households.

Keep ReadingShow less
Pop Culture

Youth choir from South Africa moves 'AGT' audience with a touching tribute to Nightbirde

The group was so inspired by the former 'AGT' contestant that they sang her song, "It's OK," leaving everyone in tears.

America's Got Talent/Youtube

Mzansi Youth Choir received a Golden Buzzer for their cover of Nightbirde's "It's OK."

Season 18 of “America’s Got Talent” kicked off on May 30th, and one of the most memorable acts of the night came in the form of a touching tribute to a former well-loved ‘AGT’ contestant.

Hailing from South Africa, the all-white-clad Mzansi Youth Choir began a capella singing “It’s OK,” which was instantly recognized as a tune created by Nightbirde—a young woman remembered not only for her lovely singing voice, but also for her incredible emotional resilience.

Back in 2021, Nightbirde arrived on the stage with only a 2% chance of surviving a third round of cancer. But still, she kept to her philosophy of "You can't wait until life isn't hard anymore before you decide to be happy." She passed away in Feb 2022, but not before sharing her beautiful heart with the world.
Keep ReadingShow less
Photo by Tod Perry

A recreation of the note left on Brooke Lacey's car.

If you are having thoughts about taking your own life, or know of anyone who is in need of help, please call the National Suicide Prevention Lifeline at 1-800-273-TALK (273-8255) or text "HOME" to the Crisis Text Line: 741741.


There’s an old Hebrew saying that if you “save one life, you save the world entire.” Who knows if Brooke Lacey, 22, had that lofty goal when she began a campaign in 2020 to help uplift people’s spirits during the first COVID-19 wave.

But her kind efforts may have done just that.

Lacey has struggled with mental health issues throughout her life and she knew that people like her were going to have a really hard time during COVID-19 lockdowns. A study from May 2021 found that the New Zealand population had “higher depression and anxiety compared with population norms.” The study also found that “younger people” and “those most at risk of COVID-19 reported poorer mental health.”

Keep ReadingShow less