What is Huntington’s Disease?

Huntington’s disease (HD) is a rare, inherited disorder that causes the progressive deterioration of nerve cells in certain parts of the brain.

It is classified as a neurodegenerative disorder, meaning it occurs when nerve cells die or are damaged due to genetic factors. HD affects individuals of all genders and ethnic backgrounds, though it is most commonly diagnosed in people between 35 and 44 years old. People with HD often experience cognitive difficulties, movement disorders, behavioural changes and psychiatric symptoms.

Kinsa Care Approach to Huntington’s Disease

Patients with Acquired Brain Injury may face immense challenges as they recover from their trauma. In addition to physical complications arising from paralysis or sensory impairments, patients may struggle with psychological issues like depression or anxiety due to alterations in their personality caused by the injury itself. Changes in behaviour can make social situations difficult for those living with ABI, as well as for friends and family members trying to support them throughout recovery. Other forms of difficulty include confusion and memory problems due to the disruption of neural networks in the brain and difficulty retaining information.