Pain in Sickle Cell Disease SIG
Purpose
The focus of the Pain in Sickle Cell Disease SIG will be to foster the development of a multidisciplinary community that brings together a diverse group of pain researchers including basic scientists, clinicians and other health professionals to increase the knowledge of pain in sickle cell disease, and to transform clinical practice and public policy to reduce pain-related suffering in children and adults with this disorder.
Leadership
Chair: Carlton Dampier, MD
Professor of Pediatrics
Emory University
Aflac Cancer and Blood Disorders Center
2015 Uppergate Dr. Room 464
Atlanta. GA 30322
404.727.4510
Communication Tool
Membership in the Pain in Sickle Cell Disease SIG allows you the benefit of participating in an APS-sponsored listserv. This forum offers community members an exchange for sharing best practices, asking questions, offering helpful information, and networking. To post a message to all members, send an e-mail to APSSickleCellSIG@lists.americanpainsociety.org.
Please keep in mind that you can only send messages to the listserv from the e-mail address you provided in your member profile. If you are having difficulties using this listserv, please e-mail the APS Listserv Administrator at list@americanpainsociety.org.
Save the Date
2019 Scientific Meeting
Milwaukee, WI
April 3-6
Additional Resources
To join this SIG, contact the APS National Office at list@americanpainsociety.org.
Basic Science | Clinical Trials | Complementary and Alternative Medicine | Ethics | Genetics and Pain | Geriatric Pain | Measurement of Pain and Its Impact | VA/DoD | Nursing | Pain and Disparities | Pain Education | Pain in Infants, Children, and Adolescents | Pain Rehabilitation | Primary Care | Psychosocial Research | Pain in Sickle Cell Disease
