“Other Cancer Survivors”: The Impact on Family and CaregiversGolant, Mitch PhD; Haskins, Natalie V. MATThe Cancer Journal: November-December 2008 - Volume 14 - Issue 6 - p 420-424 doi: 10.1097/PPO.0b013e31818d894a Special Issue on Late and Long-Term Medical Problems for Cancer Survivors: Original Article Buy Abstract Author InformationAuthors Article MetricsMetrics Care for cancer patients has changed significantly over the past 10 years and in turn, the pressure on family caregivers of these patients is increasing. The trend toward community-based medical facilities, shorter hospital stays, and growing survivorship rates all contribute to the growing burden on family caregivers. To best address the needs of caregivers, the psychosocial oncology community must seek a deeper understanding of caregiver burden and develop strategies to manage the stress that is a result of this burden. Toward this goal, The Wellness Community in partnership with the National Coalition for Cancer Survivorship conducted and reported on a national survey of over 500 caregivers to look at the psychosocial impact of the disease on caregivers. The findings from this survey as well as data from The Wellness Community’s online support group research were used to outline recommendations to better meet caregivers and patients. From the The Wellness Community, Washington, DC. Correspondence: Natalie Victoria Haskins, MAT, 919 18th Street, NW, Suite 54, Washington, DC 20006. E-mail: email@example.com. © 2008 Lippincott Williams & Wilkins, Inc.