Brooke Eby Wikipedia: Age, ALS, Career and Life

Brooke Eby was an American business development professional, social media creator and ALS advocate who became widely known for documenting her experience with amyotrophic lateral sclerosis through humor, education and personal storytelling.

Born on December 22, 1988, in Potomac, Maryland, Eby built a career in business development before becoming a prominent online voice for people living with ALS. She worked at Salesforce for about a decade and used her growing social-media audience to explain the realities of a disease that she had once associated mainly with older people.

Eby died at age 37 after living with ALS for more than four years following her diagnosis in March 2022. The ALS Network announced her death on October 1, 2026, describing her as an advocate, storyteller, community builder and friend.

Latest Update: October 2, 2026

As of October 2, 2026, Brooke Eby has died at the age of 37. The ALS Network announced her death on October 1, 2026, while tributes also came from Salesforce CEO Marc Benioff and others who knew her through her advocacy and professional career.

Eby was diagnosed with ALS in March 2022 at age 33. She spent the following four years sharing her experience with the disease online, including changes to her mobility, breathing, swallowing and speech. Her final years were marked by an increasingly large social-media audience and continued work to connect people living with ALS.

Her death followed a period in which she had openly documented the progression of her illness. In September 2026, she shared that her speech had deteriorated rapidly and that people were increasingly unable to understand her.

Who Was Brooke Eby?

Brooke Eby was an American business development manager and social media personality best known for her ALS advocacy. Her online identity was closely associated with the username @LimpBroozkit, under which she posted candid and often humorous videos about living with ALS.

Her approach was unusual because she frequently used humor while discussing an incurable neurological disease. Rather than presenting ALS only through medical explanations, Eby showed her audience what daily life with the condition could look like for a younger adult.

Her public work eventually reached hundreds of thousands of people on social media. She also founded ALStogether, a community intended to help people with ALS and their caregivers connect with resources and one another.

Brooke Eby Age and Birth

Brooke Eby was born on December 22, 1988, in Potomac, Maryland, United States. She was 37 years old when she died in 2026.

Her age became an important part of her public advocacy because ALS is often associated in the public mind with older adults. Eby repeatedly used her own experience to demonstrate that the disease can also affect younger people.

She was 29 when she first noticed symptoms in 2018 and 33 when she received her formal ALS diagnosis in March 2022.

Early Life and Education

Eby grew up in Potomac, Maryland, and later attended Lehigh University. She graduated from Lehigh in 2010. Her professional background was primarily in business development, sales and technology rather than entertainment.

Before becoming known for ALS advocacy, Eby worked in the corporate world and developed a career in sales and business development. She eventually moved between major U.S. cities, including New York and San Francisco, as her professional career progressed.

Brooke Eby’s Career Before ALS Advocacy

Eby’s career was centered on business development and technology. In 2016, she joined Salesforce, where she worked in business development and sales-related positions.

Salesforce identified her role as an ISV Principal Business Development Manager within its sales organization. In a company profile, Eby said she had been with Salesforce for nearly eight years at the time of the interview.

Her ALS symptoms began while she was working in New York City. In 2018, she noticed that she was having difficulty walking and developed what she initially believed might be a minor physical problem.

Her condition progressed slowly enough that doctors initially struggled to identify its cause. She underwent numerous tests, including imaging, blood tests, spinal taps and other neurological examinations before receiving a definitive diagnosis years later.

Brooke Eby’s ALS Diagnosis

Eby was officially diagnosed with amyotrophic lateral sclerosis, commonly known as ALS or Lou Gehrig’s disease, in March 2022.

She was 33 years old at the time. According to accounts from Eby and ALS organizations, her symptoms had begun approximately four years earlier with weakness and difficulty walking. The disease eventually affected additional parts of her body.

The diagnosis changed the direction of her public life. Instead of keeping her experience private, Eby began using social media to document what she was experiencing and to make conversations about ALS more accessible.

Why Brooke Eby Became Famous

Eby gained attention through her social-media account LimpBroozkit. Her content combined personal updates, humor, practical information and explanations about ALS.

She did not present herself solely as a medical educator. Instead, she showed everyday experiences such as using mobility aids, dealing with changes in physical ability, navigating relationships and adapting to the realities of a progressive disease.

Her humor became one of the defining features of her online presence. The ALS Association noted that Eby used jokes to make difficult conversations easier for people to approach and encouraged her audience to ask questions about the disease.

By 2025, her platforms had attracted hundreds of thousands of followers, giving her a substantial audience for ALS awareness and fundraising.

Brooke Eby and ALStogether

One of Eby’s major projects was ALStogether, a community she founded to support people living with ALS and their caregivers.

The project was designed as a place where people could find information and connect with others who understood the practical challenges associated with the disease. It also reflected Eby’s belief that people newly diagnosed with ALS needed accessible information and a community around them.

Her advocacy extended beyond social media. She participated in public speaking and ALS-related events and supported fundraising efforts for research and awareness. The ALS Association reported that she had helped raise substantial funds for ALS research through her public advocacy.

Brooke Eby’s ALS Symptoms and Disease Progression

Eby’s ALS journey unfolded over several years, and she regularly documented changes in her physical abilities.

Her first symptoms appeared in 2018, when she noticed weakness and difficulty walking. Over time, she moved from walking independently to using mobility aids and eventually a wheelchair.

In 2025, she discussed declining breathing capacity and the increasing role of respiratory support. By January 2026, she was also reporting bulbar symptoms, including difficulty swallowing, speech disturbances and increased saliva.

In September 2026, Eby publicly discussed a major change in her ability to speak. She said that while people had been asking her to repeat herself for months, her speech had become much harder to understand in the weeks leading up to her September update.

She continued making videos despite these changes, maintaining the direct and humorous style that had become associated with her advocacy.

Brooke Eby’s Final Public Updates

One of Eby’s final major public updates focused on her declining speech. In a video published in early September 2026, she explained that she felt as though she had lost her voice rapidly.

She described needing to position her head and neck carefully to produce words. She also discussed uncertainty about whether the change was related to weakened breathing or muscles around her mouth.

Although she used humor in the video, she also spoke openly about how difficult the development was for her. The update reflected the balance that had characterized much of her public ALS journey: humor alongside direct discussion of fear, loss and frustration.

Brooke Eby Family and Parents

Eby maintained a close relationship with her family, who became increasingly involved in supporting her as ALS progressed.

In 2024, reports said she moved back to her parents’ home in Potomac as she required additional assistance. Her family members also appeared in some of her social-media content.

Public sources do not provide a complete verified biography of every member of Eby’s family. For that reason, specific claims about her parents’ occupations, exact ages or other private details should not be added without reliable documentation.

Brooke Eby Husband, Boyfriend and Relationships

Eby’s personal relationships occasionally appeared in her social-media discussions, particularly as she addressed the realities of dating while living with ALS.

However, a complete and consistently verified public record of her marital status or spouse is not available in the major biographical sources reviewed for this profile. She should therefore not be described as married unless supported by a reliable source.

Her openness about dating with ALS became part of her broader advocacy because she wanted younger people with the disease to see that relationships, friendship and ordinary life continue to matter after a diagnosis.

Brooke Eby Religion

Eby’s religious beliefs are not sufficiently documented in the reliable biographical sources reviewed for this article. There is no need to assign a religion or denomination without a verified public statement from Eby herself.

Brooke Eby Height

A reliably documented official height for Brooke Eby is not established in the primary sources reviewed. Online biography sites may publish measurements, but those figures should not automatically be treated as confirmed.

Brooke Eby Net Worth

There is no reliably verified public figure for Brooke Eby’s net worth.

Her career at Salesforce provided her with a professional income before and during her ALS journey, while her social-media presence, advocacy and fundraising activities increased her public profile. However, those facts do not provide enough information to calculate her personal wealth.

Online estimates of celebrity or influencer net worth frequently rely on assumptions about salaries, sponsorships, assets and advertising revenue. Unless Eby or a reliable financial source disclosed a figure, a specific net-worth number would be speculative.

Brooke Eby Social Media

Eby’s social-media identity was closely associated with the username LimpBroozkit. She used platforms including TikTok and Instagram to document her ALS experience and communicate directly with followers.

Her accounts became an important part of her advocacy because they allowed viewers to see how ALS affected everyday life over time. Her content also challenged common assumptions about who develops the disease.

Her public presence continued even as speaking and mobility became increasingly difficult. Eby had previously expressed the hope that her videos would remain available as a resource for people diagnosed with ALS after her death.

Brooke Eby Quick Profile

Brooke Eby’s Legacy

Eby’s significance came from the way she changed the conversation around ALS for a large online audience.

She showed that a person can discuss an incurable disease without reducing their identity to a diagnosis. Her videos covered humor, friendship, relationships, work, family, disability and everyday frustrations alongside medical developments.

The ALS Network said following her death that she changed how people viewed ALS and helped people living with the disease find and support one another. Salesforce CEO Marc Benioff also publicly paid tribute to her, noting her decade-long connection with the company.

Her work with ALStogether further extended that legacy beyond individual social-media posts. The community was intended to connect people living with ALS, caregivers, experts, providers and organizations.

Reader Questions

Who was Brooke Eby?

Brooke Eby was an American business development professional and social media creator known for documenting her experience with ALS. She became a prominent ALS advocate through her LimpBroozkit social-media accounts and ALStogether community.

How old was Brooke Eby when she died?

Brooke Eby was 37 years old when she died in October 2026. She was born on December 22, 1988.

When was Brooke Eby diagnosed with ALS?

Eby was diagnosed with ALS in March 2022 at age 33. Her first symptoms had appeared approximately four years earlier, beginning with weakness and difficulty walking.

What was Brooke Eby’s job?

Before becoming widely known as an ALS advocate, Eby worked in business development and sales. She joined Salesforce in 2016 and ultimately worked as an ISV Principal Business Development Manager.

What is Brooke Eby known for?

She was best known for sharing her ALS journey online through the LimpBroozkit accounts. Her content combined humor, personal storytelling, education and advocacy for people living with ALS.

What was ALStogether?

ALStogether was a community founded by Eby to help people with ALS and their caregivers connect with resources, professionals and other members of the ALS community. It became one of her major advocacy projects.

Did Brooke Eby have ALS?

Yes. Eby was diagnosed with amyotrophic lateral sclerosis in March 2022 at age 33. She publicly documented the disease’s progression for more than four years.

What happened to Brooke Eby?

Brooke Eby died at age 37 in October 2026 after living with ALS since her diagnosis in 2022. The ALS Network announced her death on October 1, 2026.

What was Brooke Eby’s TikTok name?

Her social-media username was LimpBroozkit. She used the account to share her daily experiences with ALS and raise awareness about the disease.

What was Brooke Eby’s net worth?

Her exact net worth was not publicly verified. Although she had a long professional career at Salesforce and a substantial social-media presence, there is not enough reliable financial information to establish a precise figure.

Wrap-Up

Brooke Eby built her public identity around an experience she initially had no reason to expect would become the defining subject of her career. After noticing weakness in 2018 and spending years seeking an explanation, she was diagnosed with ALS at age 33 in March 2022.

She then used social media to make ALS more understandable to people who might otherwise never encounter the disease. Her combination of humor, honesty and education helped her reach hundreds of thousands of people while also supporting fundraising and community-building efforts.

Eby’s death at age 37 on October 1, 2026, brought an end to the life she had spent documenting so openly. Her videos, advocacy work and ALStogether community remain important parts of the public record she created around living with ALS.