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Scoliosis Research Society (SRS)
An International Organization Dedicated to the Education, Research and Treatment of Spinal Deformity
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Scoliosis Research Society (SRS)
An International Organization Dedicated to the Education, Research and Treatment of Spinal Deformity
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The SRS is an International Association
Scoliosis Research Society
555 East Wells Street, Suite 1100
Milwaukee, WI 53202-3823 USA
[ MAP ]
Phone: (414) 289-9107
Fax: (414) 276-3349
Email: info@srs.org
Web: srs.org
Office hours:
Monday - Friday
8:00am to 5:00pm, Central Time
Executive Director
Tressa Goulding, CAE, CMP
tgoulding@srs.org
Staff
Meetings Coordinator
Cydni Chapman
cchapman@srs.org
Annual Meeting, Awards, IMAST, Website
Meetings Director
Megan Kelley
mkelley@srs.org
Annual Meeting, IMAST, Corporate Support, Program
Executive Assistant
Courtney Kissinger
ckissinger@srs.org
Board of Directors, Bylaws & Policies, CME, Directed Research, Spine Deformity Journal
Program Coordinator
Katy Kujala-Korpela
kkujala-korpela@srs.org
Patient Inquiries, Historical Society Information, SRS Newsletter, E-Text, Endowment
Program Manager
Brian Lueth
blueth@srs.org
Advocacy, Education, Membership, Research Grants
Membership Manager
Nilda Toro
ntoro@srs.org
Membership, Morbidity & Mortality Reporting, Member Passwords
The Scoliosis Research Society provides information on these web pages regarding research and links as a public service. The SRS believes that patients should contact their treating physician about the relevance of any information listed on the site prior to proceeding with any particular treatment. Just as no two individuals are exactly alike, no two patients with a spinal deformity are the same. Therefore, your spinal deformity surgeon will be the most important source of information about the management of your particular spinal problem.