
Lewy Body Dementia (LBD) is a brain disease that’s often misunderstood. It’s actually the second most common type of progressive dementia after Alzheimer’s disease (AD). For patients and families, learning what LBD is, how it differs from other dementias, and how to manage its symptoms can make a huge difference in planning care and finding support.
LBD happens when abnormal protein clumps—called Lewy bodies—build up inside brain cells. These clumps are made of a protein called alpha-synuclein. Over time, they interfere with how brain cells communicate and work, leading to problems with memory, thinking, movement, and behavior. We spoke with neurologist and author Dr. Carolyn Larkin Taylor, who has treated patients with LBD for over 30 years. In her memoir, Whispers of the Mind: A Neurologist’s Memoir, she shares both medical insight and the deeply human side of caring for people with this condition. “Treating these patients inspired me so much because of their courage,” Dr. Taylor says. “I wanted to show readers that we all share a common humanity—and that the human spirit is more resilient than we ever knew.” RELATED: Is it Alzheimer’s or Forgetfulness? 5 Signs to Tell
LBD and Alzheimer’s both cause memory loss and confusion, but they affect the brain in different ways and often progress differently. Knowing which type of dementia you’re dealing with helps families plan and understand what to expect. “People sometimes think dementia is just dementia—but it’s important to know which kind. Each type has different symptoms and needs. An accurate diagnosis helps families better manage care and support,” Dr. Taylor explains. It’s also worth noting that LBD and Alzheimer’s can occur together, which makes diagnosis more challenging. The only way to confirm LBD for sure is by examining brain tissue after death, but doctors can make a strong clinical diagnosis based on symptoms. RELATED: Alzheimer’s vs. Other Dementias: What’s the Difference?

LBD often shows up with both memory problems and movement issues similar to Parkinson’s disease. Doctors look for several hallmark signs:
People with LBD can have dramatic ups and downs in their alertness—one moment they’re engaged and clear, and the next they’re drowsy, staring, or confused.
Seeing things that aren’t there (like people or animals) is very common. These hallucinations can be vivid and realistic, and sometimes frightening.
Many patients develop slowness, stiffness, and balance problems. Tremors may or may not occur.
This can be one of the earliest signs of LBD. People physically act out their dreams—talking, shouting, punching, or kicking during sleep. Sometimes they fall out of bed or accidentally hurt their bed partner. “Patients often describe dreams where they’re fighting off an attacker,” Dr. Taylor says. “Bed partners may report being hit or kicked, and sometimes the person wakes up on the floor.” LBD is more common in men, possibly because estrogen may help protect women’s brains from the buildup of these abnormal proteins.
LBD shares symptoms with both Alzheimer’s and Parkinson’s diseases, as well as certain psychiatric conditions. This overlap can make diagnosis tricky.
“When patients with LBD are given typical antipsychotics, their symptoms often get worse,” Dr. Taylor says. “That’s an important clue that it’s not a primary psychiatric disorder.”
There’s currently no cure for LBD, but many symptoms can be managed with supportive care and understanding. The main focus is keeping the patient safe, comfortable, and emotionally supported—while helping caregivers avoid burnout.
Continuous reassurance is key,” according to Dr. Taylor.
Eventually, many patients will need care in a specialized facility that understands LBD.
Research into LBD is growing fast. Scientists are working on ways to diagnose it earlier and develop treatments that stop the buildup of alpha-synuclein in the brain. While there’s no cure yet, there is real hope for the future—and plenty that families can do right now to improve quality of life and keep loved ones safe, understood, and supported.


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