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Hereditary Hemorrhagic Telangiectasia

This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.

HHT Foundation International, Inc.

International. Founded 1991. Mutual support and education for persons interested in hereditary hemorrhagic telangiectasia (aka Osler-Weber-Rendu syndrome). Supports clinical and genetic research. Counseling and advice for patients. Referrals to appropriate treatment centers. Annual patient/doctor conference. Tri-annual newsletter 'Direct Connection.' Aims to protect all members under the Right To Privacy Act.
Write:
HHT Foundation International, Inc.
P.O. Box 329
Monkton, MD 21111
Voice: 410-357-9932
Fax: 410-357-0655
Website: http://www.hht.org
E-mail: hhtinfo@hht.org
Verified: 8/13/2013

WebMD Medical Reference from the American Self-Help Clearinghouse

Last Updated: September 04, 2014
This information is provided as a resource and does not constitute an endorsement for any group.  It is the responsibility of the reader to decide whether a group is appropriate for his/her needs.  For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.This information is not intended to replace the advice of a doctor. Healthwise disclaims any liability for the decisions you make based on this information.   

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