'Palliative care' means more than 'end-of-life' care for children and families coping with muscle disease
posted on July 1, 2009 - 11:06am
Families face complicated health care decisions when coping with a child’s neuromuscular disease, and the best course of action isn’t always clear. Often, the child’s doctors are in uncharted territory too.
Now, MDA is trying to provide a road map through this confusing, emotional time by offering families and physicians enhanced “palliative care” services for the children it serves.