Huntington's Disease Society of America
Northeast Ohio Chapter

Genetic Testing Centers in Northeast Ohio approved by the HDSA

Center for Human Genetics
University Hospitals of Cleveland
Arthur B. Zinn, M.D., Ph.D.
(216) 844-3936

Genetics Center
MetroHealth Medical Center, Cleveland
Carol A. Crowe, M.D.
(216) 778-4323

Genetics Center
Children's Hospital, Akron
Haynes Robinson, M.D.
(330) 543-8792

Huntington's Disease Society of America Dr. George Sumner and the Disease Bearing His Name by John P. Conomy, M.D., J.D. Huntington's Disease Society of America: a Brief History of People and Programs 1967-1997 Genetic Testing for HD: A Guide for Families Huntington's Disease: A Disease of Mind and Body (A Case for Support) More Resources on the Web
The National Research Roster for HD Patients and Families is a nationwide registry and information resource dedicated to assisting scientific research on HD. The Roster identifies HD patients and families who are interested in participating in research projects to help scientists learn more about HD. The Roster has involved nearly 3,000 families in HD research.

The Indiana University DNA Bank was established as the world’s first DNA bank in 1984. The DNA bank was created so that individuals and families could store DNA samples that may be needed for future genetic testing.

For more information about the Roster or the DNA bank, please visit http://hdroster.iu.edu or contact the coordinator by calling (317) 274-5744 or email pswolf@iupui.edu
Make this the last generation of HD.
Your support and understanding can make a difference. There are many ways to help find the cure. So, please, don't delay, call HDSA today! Or, contact the local chapter in your area.

Barbara Kaiser – Development Director
HDSA Northeast Ohio Chapter
10176 Luman Lane
Twinsburg, OH 44087
bkaiser@HDSA.org
Phone: 330-998-6600
Fax: 330-998-6677

Presented by Lakewood Public Library