In tandem with recent progress in basic and clinical research in amyotrophi
c lateral sclerosis (ALS), clinical care and management has improved substa
ntially, Key processes and practices have been established and are specifie
d in current ALS Practice Parameters; the international ALS databases ident
ify the current status of care and management given by physicians. A number
of prospective clinical management research studies are now well underway
to establish the effective utility of enteral feeding, assistive ventilator
y device, and exercise in patients with ALS. One of the main research objec
tives in the clinical management of ALS is to improve patients' quality of
life. For patients with ALS, only comprehensive multidisciplinary care can
effectively improve their overall quality of life from diagnosis to death.
This paper will briefly review a number of factors that must be considered
if we are to improve the quality of life for these patients, including comp
rehensive medical management, patient education, the importance of hope, th
e role of the health care professional, and the patients themselves.