Increased Depression, Burden, Reported in Family Caregivers of ALS Patients
American Academy of Neurology (AAN)Family caregivers of people with ALS, most often spouses, are likely to become depressed and feel burdened, but that's not the case for the people they are caring for, according to a study published in the March 20, 2007, issue of Neurology, the scientific journal of the American Academy of Neurology.