From diagnosis to daily life:
Navigating Huntington's disease

Talking to children about Huntington’s disease means starting honest, age-appropriate conversations early. Keeping the dialogue open helps kids feel more secure and supported as the condition progresses.

Support groups and community resources for Huntington’s disease can offer meaningful connection, emotional support, and reliable information for people living with HD and their caregivers.

Huntington’s disease disrupts sleep, worsening cognitive decline and emotional distress. Managing sleep with consistent routines, relaxation techniques, and medical support can improve rest, daily functioning, and overall well-being.

An early Huntington’s diagnosis helps patients access symptom management resources, improve their overall quality of life, and make informed plans for the future. Advancements in genetic testing have made early detection more accurate.

As Huntington’s disease advances, symptoms related to movement, cognition, and behavior become increasingly pronounced. Greater awareness of each stage supports more effective care planning.

Adaptive devices can help make daily life with Huntington’s disease more manageable by enhancing mobility, improving communication, and simplifying everyday tasks, thereby promoting safety, comfort, and greater independence.

Genetic testing for Huntington’s identifies HTT gene mutations, aiding in diagnosis and family planning. Genetic counselors can guide you through the process and its emotional impacts.

Chorea, involving involuntary muscle movements, is linked to Huntington’s disease but can occur in other conditions too. Understanding their connection can help manage symptoms.

A Huntington’s diet focused on nutrient-dense, high-calorie foods and supportive meal strategies can help maintain weight and ease mealtime challenges caused by swallowing difficulties.