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HHT Foundation International, Inc.

Rare Diseases are celebrated in today's Washington Post supplement!
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Today, there is a special supplement in the Washington Post celebrating Rare Diseases and the 30 year anniversary of the passage of the Orphan Drug Act in Congress.  READ the full supplement. 


 
HHT Awareness will save lives! 
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The HHT Foundation has invested in it's first national HHT Awareness Ad Campaign. 
 
Our ad is located on page 2 just below the message from the National Organization for Rare Disorders (NORD). Remember, 9 out of 10 people who have HHT don't know they have it. They could be your next door neighbor, classmate, co-worker, or family member.

Awareness is the key to early diagnosis and treatment which will ultimately save lives.
 
Please pass this email on to everyone you know, including your doctors and congressional representatives, by clicking on the SHARE button below. We guarantee you will impact someone's life. We appreciate your support! 
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HHT Foundation International, Inc.                 www.hht.org

Our mission is to find a cure for HHT while saving the lives and improving the well-being of individuals and families affected by this disease. We are a member-funded non-profit organization that achieves it's mission by funding research, educating families and physicians, providing linkages between people affected by HHT, collaborating with HHT treatment centers worldwide, advocating for federal involvement, and engaging the scientific and medical community.  

Our accomplishments are made possible through the generous donations of our members and those who have contributed on their behalf.  We need your continued support.