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102-year-old woman discovers that she's a surviving member of special WWII unit

Crescensia Garcia is getting the recognition she deserves.

army, 102-year-old woman, twitter, crescensia garcia
CBS Mornings/YouTube

A 102-year-old woman's family learned something about her past military service thanks to Twitter.

You never know when you have a legend in your family. Two years ago, a woman named Tara Garcia reached out to "CBS Mornings" correspondent David Begnaud to share a story. Her grandmother, Crescensia Garcia, had just turned 100 and had recently survived COVID-19, only having to briefly use oxygen. Begnaud shared the story of the elder Ms. Garcia with his followers on Twitter, including some pictures Tara had sent him. Little did they know, a bigger story was about to unfold.


Edna Cummings, a retired Army colonel, saw Begnaud's tweet. One of the pictures Tara had sent him was of her grandmother in her military uniform. Cummings told "CBS Mornings" that seeing the photo of Crescensia "was like being in a casino and hitting the jackpot." Why? Turns out Crescensia was part of a very special military unit during World War II.

Cummings needed to know Crescensia's dog tag numbers to confirm her suspicions, so she reached out to Tara. After receiving them, Cummings was able to confirm that Crescensia was part of a burn unit located near Birmingham, England, which treated wounded soldiers due to a shortage of people in the area who could perform those procedures. She may not have thought much of it at the time (it was her military duty after all), but Crescensia Garcia was part of something special.

The SixTripleEight was an 855-member unit that was all Black and all women. Of course, the unit was segregated, but that didn't stop the members from serving their country. Crescensia Garcia, who is now 102 years old, is one of only six surviving members of the unit. And her family had no idea.

"They're the only military women's unit to receive a congressional gold medal," Cummings told "CBS Mornings." "They are part of an elite group of less than 200 recipients. The first being General George Washington." In addition to receiving the congressional gold medal, the family learned that Crescensia's name is on a World War II monument along with other veterans, in Fort Leavenworth, Kansas.

When Tara Garcia found out this information, "I looked at my parents and said, 'I think we just opened Pandora's box here,'" she said. The revelation certainly led to some very cool opportunities, including meeting first lady Dr. Jill Biden.

Both Crescensia and Tara Garcia sat down with David Begnaud on "CBS Mornings" to talk about their family and it was truly the sweetest thing. Although she's beginning to show signs of her age, Crescensia is still pretty sharp and a truly beautiful soul.

Crescensia was born in Puerto Rico in April 1920, before women even had the right to vote. At that time, a loaf of bread was less than 20 cents! She moved to New York City in her youth, and at the age of 24 she enlisted in the Army because the bombing of Pearl Harbor made her so enraged that she felt it was her civic duty to serve and protect. She was immediately put in an all-Black unit for her basic training in Texas.

"They put me in the Black section and there is a White section. That's America to you. See? That's America to you and it's very sad, very sad," she told Begnaud. After the segment, he explained to the news desk that the reason she was able to become a medic was due to her light skin color. She was able to "pass" as white, which earned her privilege.

Social media post helps woman discover her grandmother's World War II past

Much like others who have served in war, Crescensia doesn't seem to think her time in the Army was anything special. She told Begnaud that she was "just" a medic and was only doing her job tending to the injured.

"I am proud to be an American," she said.

After the war, she went back to New York City, settling in the Bronx and getting married and having three children. She became a seamstress, working in Manhattan's Garment District. Now, she is living her best life and sharing her story with the world.

During their interview, Begnaud explained that he had a surprise for both women. He had gotten in touch with the White House and arranged for Dr. Jill Biden to call and FaceTime with them.

"You are one incredible woman and I can't thank you enough for all your service to our country," Dr. Biden said warmly.

"And I salute you. Keep it up. Keep up the good work," Crescensia said, raising her hand to salute the first lady.

At 102, her memory isn't what it used to be, but, according to Tara, her presence of mind during the interview and conversation with the first lady is something neither of them will forget.

"The fact that she knew who that was. Yeah, and she felt that acknowledgment just now. That's all I needed. That's all I needed. I just want her to remember, that's all," Tara said.

We salute Crescensia Garcia and thank her for being who she is.

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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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