Membership

SIG: Pain in Sickle Cell Disease

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: Assistant Dean for Clinical Research
St. Christopher’s Hospital for Children
Office for Clinical Research
1599 Clifton Rd NE
Mailstop 1599-001-1AG
Atlanta. GA 30322
404-778-2561

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.ampainsoc.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@ampainsoc.org.

APS Scientific Meeting

Mark your Calendars: 2012 APS Scientific Meeting
May 16-19, 2012
Honolulu, HI

The Pain in Sickle Cell Disease SIG will meet in Hawaii May 17th from 4:15-5:15 P.M.

2011 APS Scientific Meeting
May 19-21, 2011
Austin, TX

Additional Resources

Join the SIG

Contact the APS national office at list@ampainsoc.org.