Contact HHT Foundation International, Inc. for event and ticket information.
Does HHT run in your family?
Do you wish that there were people focused on HHT research and education?
If the answer is yes to both of these questions, then I ask that you ask yourself "How can one person help raise awareness and advance treatment and research?" The government is not going to do it.....so it is up to each one of us to do whatever we can to help in this effort.
I ask you to consider supporting the efforts of those who have accepted the challenge to run in the Race for HHT Awareness in October. The HHT office will be running in the Baltimore, MD Marathon and an active Board member is running in the Long Beach, CA Marathon all to benefit HHT. But, we can't do this alone: WE NEED YOUR HELP!
Please consider making a contribution to help in this effort which will advance our cause. You can choose to support either marathon. All proceeds ultimately benefit those affected with HHT.
Thank you for your support.
Marianne S. Clancy, Executive Director, HHT Foundation International, Inc.
If Not US, Who?
If Not NOW, When?
HHT Foundation International is a worldwide, non-profit organization whose purpose is to support patients and families and educate medical professionals. We are dedicated to the individuals and medical professionals who encounter the daily challenges of managing Hereditary Hemorrhagic Telangiectasia (HHT) also known as Osler-Weber-Rendu Syndrome.
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