Pain in persons with severe dementia is often not recognized or treated because these persons cannot communicate their needs. Family caregivers are in the best position to provide information to hospital care personnel about the patients' needs, including pain. Little research has evaluated the role of the family caregiver when patients move between care facilities. This study describes family caregivers' experiences when their family members with dementia were admitted to unfamiliar care sites and provides the caregivers' recommended changes to healthcare settings. This article is relevant to family members and healthcare professionals who care for persons with severe dementia.

The Journal of Rehabilitation Research and Development (JRRD) has been a leading research journal in the field of rehabilitation medicine and technology for over 40 years. Formerly the Bulletin of Prosthetics Research, JRRD debuted in 1983 to include cross-disciplinary findings in rehabilitation. JRRD, a scientifically indexed journal, publishes original research papers, review articles, as well as clinical and technical commentary from U.S. and international researchers on all rehabilitation research disciplines.

JRRD publishes in both print and electronic formats, increasing the journal's dissemination from a hard copy circulation of 8,000 to 2.3 million Web downloads in 2005. Currently, there are over 1,000 peer-reviewed articles available in electronic format and free for downloading. JRRD will initiate an archiving program in 2005 to make all issues of JRRD and the Bulletin of Prosthetics Research available online.

Journal of Rehabilitation Research and Development
Now Available Online and in Print: www.rehab.research.va