Brooke Eby shared her life with ALS online, but her account was more than a diary

Brooke Eby, who went by the online handle LimpBroozkit, lived with amyotrophic lateral sclerosis (ALS) for many years before her death at the age of 37. She gained notoriety by sharing her journey with the disease on social media, using humor and frankness to build a sizable following. In 2022, Eby started posting updates about her ALS experience on TikTok under her username LimpBroozkit.

Her content quickly gained traction, attracting hundreds of thousands of fans who appreciated her willingness to openly discuss disability, healthcare, and identity.

Eby's approach to sharing her ALS diagnosis was characterized by levity and candor. She once said to Today in 2023, "Levity is my superpower," which became a defining trait of her content. Even as her condition worsened, Eby continued to use humor to navigate her illness. Her ability to balance humor with honesty resonated with viewers, allowing them to connect with her on both personal and communal levels.

Beyond her platform, Eby's influence extended to creating ALStogether, a nonprofit organization aimed at connecting people diagnosed with ALS with resources, experts, caregivers, and each other. Her dedication to building a supportive community is evident in the comments section of her posts, where followers often share their own experiences, fostering a sense of solidarity and understanding.

Eby's impact goes beyond her personal diary; it represents a broader trend in social media where individuals use platforms not just for entertainment, but for education and connection. Through her honest portrayal of life with ALS, Eby has played a significant role in shifting societal attitudes towards chronic illnesses and accessibility. Her legacy continues to inspire and educate, leaving a lasting impact on those who followed her journey online.