Als Girls

Als Girls
Her ALS Story seeks to raise awareness that ALS impacts young women diagnosed before 35 and provide a community for them to connect, learn from each other, and find support so they can live their best lives.
Older females may experience more early symptoms of ALS in the bulbar region of their brain, which controls facial and neck muscles. Learn more here.
Though ALS may be less common in women, the disease is no less debilitating. Learn about ALS symptoms in women, the causes, and the outlook.
Learning she had ALS at 27 felt tough. But woman starts organization to help other young women with ALS. Hopes
Amyotrophic lateral sclerosis (ALS) is a rare neurological disorder that affects specific nerve cells in the spinal cord known as motor neurons. Symptoms involve issues with swallowing and speech ...
At ALS United Greater New York, we're committed to empowering our community with knowledge about Amyotrophic Lateral Sclerosis (ALS). This guide focuses on the early signs of ALS in females, highlighting the importance of early detection and the unique challenges women face in diagnosis and management.
The Young Faces of ALS is a group of people whose lives have been impacted by ALS. We are people with ALS, children, friends, and caregivers. We are uniting to share our stories, promote awareness of ALS, and emphasize the need to support ALS research at ALS TDI. We will work together to spread awareness until there are treatments for everyone with ALS.
New Jersey woman says her rare ALS was stopped by new drug Raziel Green, 52, an active runner and mother of two, was diagnosed with a rare form of ALS in 2017. Nearly eight years later, her ...
14K Followers, 801 Following, 794 Posts - Her ALS Story (@heralsstory) on Instagram: "We are a group of women diagnosed with ALS before our 35th birthday who are challenging the stereotype that ALS is an old white man's disease."
At just 34, Melissa faced the unimaginable: an ALS diagnosis. With two young sons and a vibrant life, she leaned on her family and the Emory Healthcare ALS Center to find strength—and purpose. Today, she's not only navigating ALS with courage, she's helping researchers uncover new hope through clinical trials.
Meteorologist Jeriann Ritter announced in an interview with Keith Murphy that doctors think she may have ALS, which could end her time at WHO 13.
The "Grey's Anatomy" and "Euphoria" actor, 53, agreed to be interviewed on the condition that the footage be released after his death.
Iowa - WHO 13 Meteorologist Jeriann Ritter says doctors believe she has amyotrophic lateral sclerosis, or ALS.Ritter explained how she's handling the news in a
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The "Grey's Anatomy" and "Euphoria" actor, 53, agreed to be interviewed on the condition that the footage be released after his death.
While it may feel like a distant memory, temperatures were in the 60s a week ago, giving construction crews the chance to get ahead on some projects around the metro ...
'Euphoria' star Eric Dane, who died on Feb. 19, 2026, and actress Rebecca Gayheart shared two children, daughters Billie and Georgia. Here's everything to know about Eric Dane's kids.
Carrigtwohill CC 2-1 St. Als, Carrigtwohill Our U17 girls were crowned Munster Champions in St. Coleman's Park on Tuesday. It was a game of high quality with both sides showing why they were playing...
Days after Eric Dane's death at age 53 following a battle with ALS, his girlfriend Janell Shirtcliff shared a glimpse inside her apparent romance with the late actor.
Eric Dane's girlfriend, Janell Shirtcliff, honored the late actor after his death at age 53 following a battle with ALS
A familiar face in Iowa television, Jeriann Ritter has announced she has been diagnosed with amyotrophic lateral sclerosis (ALS), bringing an end to her 20-year career as a meteorologist at WHO 13 in Des Moines. The 49-year-old revealed her diagnosis during an emotional on-air interview that aired ...
Professor Stephen Hawking was seen grinning from ear-to-ear as he sat sandwiched between two bikini-clad women in a photo released in the Jeffrey Epstein files.
Add Yahoo as a preferred source to see more of our stories on Google. A beloved longtime Iowa meteorologist revealed she has been diagnosed with an aggressive case of ALS - a career-ending illness ...
Her ALS Story represents only a fraction of young women with ALS. We are honored to highlight others that never got the chance to officially be a part of our group. <3
Eric Dane, known for his roles on "Grey's Anatomy" and "Euphoria," died this week from amyotrophic lateral sclerosis at age 53. The fatal nervous system disease, also known as Lou Gehrig ...
Eric Dane was feeling extreme emotions as ALS was keeping him away from his daughters. The renowned American actor, who rose to fame with his portrayal of Dr. Mark Sloan in Grey's Anatomy and...
36K Followers, 191 Following, 625 Posts - ALS Scan Official (@alsscan.official) on Instagram: "Satisfying your guilty pleasures since 1996 • Official channel of #ALSScan. Managed by @metart.network and censored to comply with Instagram's terms."
ALS Scan (TV Series 2004- ) - Cast and crew credits, including actors, actresses, directors, writers and more.
Rebecca Gayheart remained his caregiver even after their 2018 separation, telling her girls: "He is our family. We show up with dignity and grace."
Leah Stavenhagen, 29, started Her ALS Story to bring together young women with ALS and challenge the myth that it's an old person's disease.
One minute she was a fashion publicist, the next she was diagnosed with ALS, a rare and terrifying illness that's more common in men.
Brooke Eby was in her early 30s when she was diagnosed with ALS — but she is determined to show the world what it is really like to live with an incurable di...
Hear from three women how have battled ALS, or Lou Gehrig's disease. AlS does not just affect men, but women too.
Michele Stellato, featured in Matter of Mind: My ALS and diagnosed as a young woman with ALS, talks about how she uses humor to cope while she fights for research. She addresses some common myths ...
"I feel the more people that use their voices, the more attention we will bring to ALS, and the closer we will be to finding treatments and one day at a cure."
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Gayheart filed for divorce from Dane in 2018, but dismissed her petition in March 2025 just before Dane announced he had been diagnosed with ALS.
Amanda Tam, 24, was in her first year at university when she began to notice some concerning symptoms. Her grip became weak, and soon after she had trouble walking and developed debilitating ...
As an occupational therapist, Katie Adams had a keen sense of what was happening to her body when her ALS symptoms first started and was pretty sure she knew why. Little did she know her intuition would not only prove to be correct.
Lauren "Lolo" Spencer was diagnosed with ALS at 14. Now, she uses Instagram and YouTube to give advice and share her experience.
Dec 6, 2022
This blog post will discuss the various symptoms of ALS and its effects on the human body. We will also discuss causes and treatment options for ALS.
Her ALS Story and the ALS Therapy Development Institute (ALS TDI) have collaborated on a video that aims to explain the biological processes behind ALS.
My life isn't going to be what I always dreamed about, but I believe I was meant to have Lou Gehrig's disease, or ALS. When people think of ALS, the degenerative nervous system disease that ...
Sarah Langs, AB'15, hopes to bring awareness to disease, inspire other women to work in baseball
Grey's Anatomy star Eric Dane has passed away, after revealing his ALS diagnosis. Meet his wife, Rebecca Gayheart, and their two daughters, Billie and Georgia Dane.
ALS seems to be striking people who are younger and younger and doctors don't know why
Amanda has always used writing to process things. So when she faced the challenge of ALS, she started blogging about it—at first just for herself, and then for the community.
16 members of Her ALS Story joined together on a girls' trip to Wisconsin to connect in-person.
All ladies shaved
"As an organization wholly funded through philanthropy, we greatly value our partnership with the Calendar Girls of '72, their families, and communities," says Meg Whiteford, senior associate director of development at the Packard Center.
'I can tell you, up until this point, I didn't forecast this storm hitting,' meteorologist Jeriann Ritter said in an interview
Leah shares her experience being diagnosed and living with ALS. She also discusses the urgent need for advancements in science that will lead to potential tr...
I'm convinced that years of chronic stress triggered my ALS — work, perfectionism, overtraining and underfueling all combined into a neurological freakout at the cellular level.
Each year, the Hero Awards recognize special people in the ALS community who have made a significant impact for those living with the disease. People like Brooke Eby, whose approach to just about everything is to joke about it, even living with ALS.
Jill Leblanc shares the story of how she was diagnosed, and how she has been adjusting to the realities of life with the disease - and how she is managing her symptoms
Rebecca Gayheart remained his caregiver even after their 2018 separation, telling her girls: "He is our family. We show up with dignity and grace."
Erste Freundschaften entstehen! Lola, Nana, Juna und Marlene haben sich gesucht und gefunden - ab jetzt sind sie als „Spice Girls" unterwegs. 👯‍♀️ #GNTM...
At first, Her ALS Story came together and connected with each other primarily online. However, after a small group of HAS members got together at a beer festival in 2021, Kate says that they quickly recognized the uplifting power of meeting in person. Soon, they were discussing the possibility of a larger, multi-day gathering.
Brooke Eby (@limpbroozkit) on TikTok | 10.8M Likes. 244.3K Followers. just a gal with ALS Brooke@eptalent.com.Watch Brooke Eby's popular videos: "Slinggg batter batte...", "My diagnosis story #...". Join 244.3K followers on TikTok for more alsawarenessmonth, als, ad content
Amyotrophic lateral sclerosis (ALS), formerly known as Lou Gehrig's Disease, is a neurological disease that affects motor neurons—those nerve cells in the brain and spinal cord that control voluntary muscle movement.
Whether you're living with ALS, a caregiver, or a loved one, your story holds the potential to illuminate the realities of this disease, break down misconceptions, and offer a sense of solidarity to others navigating similar day-to-day challenges.
When a family is dealing with an ALS diagnosis, children/youth are often more aware than parents may realize. Thus, beginning a conversation with them about an ALS diagnosis can be very challenging. Although you may feel you do not know how to approach the conversation, it is important to be honest and direct with your children/youth. They can sense when you are stressed and may believe that ...
The ALS Association's Support and Services for people living with ALS and caregivers living in Arizona
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