Huntington’s Disease is a progressive genetic disorder that affects the brain, causing physical, cognitive, and emotional challenges. This article is a comprehensive guide that explains the disease in detail, addressing its causes, inheritance patterns, symptoms, and treatment options. It begins with an introduction to the condition, followed by a discussion of its prevalence and the different forms it can take, such as adult-onset and juvenile Huntington’s Disease. The article explores the genetic basis of the disease, focusing on the role of the HTT gene, and explains how the condition is inherited. It then provides an in-depth look at the symptoms, which include movement difficulties, memory loss, and mood changes, as well as the methods used for diagnosis, including genetic testing and brain imaging. The article outlines current treatment and management strategies, covering medications, therapies, and experimental approaches that aim to slow disease progression or alleviate symptoms. It also examines the prognosis and discusses practical aspects of living with the condition, offering guidance and resources for patients and caregivers. Organized in a logical flow, the article moves from understanding the basics to addressing daily challenges and future planning. Written in simple language, it ensures that the information is accessible and easy to understand for all readers.