ALS is a disease that changes the lives of patients and their family members. Families
confronted with a diagnosis of ALS may experience anxiety, confusion, and stress.
The following advocate organizations and social service agencies can suggest ways
to cope with the physical and emotional challenges of ALS and provide information,
assistance, and emotional support to patients, families, and caregivers. Travel
information for people with ALS is also included, as well as a reading list that
patients and their caregivers may find useful.
Click on the following links for more information:
Patient Resources
Caregiver/Family Resources
Home Care and Hospice Options
Travel Assistance
Recommended Reading